Raras
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Poliartrite juvenil
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Introdução

O que você precisa saber de cara

📋

Artrite idiopática juvenil (AIJ), anteriormente conhecida como artrite reumatoide juvenil (ARJ), é a doença reumática crônica mais comum da infância, afetando aproximadamente de 3,8 a 400 em cada 100.000 crianças. Juvenil refere-se ao início da doença antes dos 16 anos de idade, enquanto idiopática refere-se a uma condição sem causa definida, e artrite é a inflamação dentro da articulação.

Pesquisas ativas
2 ensaios
19 total registrados no ClinicalTrials.gov
Publicações científicas
253 artigos
Último publicado: 2026 Apr 9
🏥
SUS: Sem cobertura SUSScore: 0%
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Sinais e sintomas

O que aparece no corpo e com que frequência cada sintoma acontece

Partes do corpo afetadas

🦴
Ossos e articulações
15 sintomas
📏
Crescimento
3 sintomas
💪
Músculos
2 sintomas
🩸
Sangue
2 sintomas
👂
Ouvidos
1 sintomas
🫃
Digestivo
1 sintomas

+ 21 sintomas em outras categorias

Características mais comuns

Taxa de sedimentação de eritrócitos elevada
Osteoartrite do joelho
Oligoartrite
Iridociclite
Artrite poliarticular
Limitação da mobilidade articular
45sintomas
Sem dados (45)

Os sintomas variam de pessoa para pessoa. Abaixo estão as 45 características clínicas mais associadas, ordenadas por frequência.

Taxa de sedimentação de eritrócitos elevadaElevated erythrocyte sedimentation rate
Osteoartrite do joelhoKnee osteoarthritis
OligoartriteOligoarthritis
IridocicliteIridocyclitis
Artrite poliarticularPolyarticular arthritis

Linha do tempo da pesquisa

Publicações por ano — veja quando o interesse científico cresceu
Anos de pesquisa1desde 2026
Total histórico253PubMed
Últimos 10 anos164publicações
Pico202122 papers
Linha do tempo
2026Hoje · 2026🧪 2000Primeiro ensaio clínico📈 2021Ano de pico
Publicações por ano (últimos 10 anos)

Encontrou um erro ou informação desatualizada? Sugira uma correção →

Genética e causas

O que está alterado no DNA e como passa nas famílias

Genes associados

7 genes identificados com associação a esta condição.

STAT4Signal transducer and activator of transcription 4Candidate gene tested inAltamente restrito
FUNÇÃO

Transcriptional regulator mainly expressed in hematopoietic cells that plays a critical role in cellular growth, differentiation and immune response (PubMed:10961885, PubMed:37256972, PubMed:8943379). Plays a key role in the differentiation of T-helper 1 cells and the production of interferon-gamma (PubMed:12213961, PubMed:35614130). Also participates in multiple neutrophil functions including chemotaxis and production of the neutrophil extracellular traps (By similarity). After IL12 binding to

LOCALIZAÇÃO

CytoplasmNucleus

VIAS BIOLÓGICAS (5)
Interleukin-20 family signalingInterleukin-21 signalingInterleukin-12 signalingInterleukin-35 SignallingInterleukin-23 signaling
MECANISMO DE DOENÇA

Systemic lupus erythematosus 11

A chronic, relapsing, inflammatory, and often febrile multisystemic disorder of connective tissue, characterized principally by involvement of the skin, joints, kidneys and serosal membranes. It is of unknown etiology, but is thought to represent a failure of the regulatory mechanisms of the autoimmune system. The disease is marked by a wide range of system dysfunctions, an elevated erythrocyte sedimentation rate, and the formation of LE cells in the blood or bone marrow.

EXPRESSÃO TECIDUAL(Ubíquo)
Testículo
34.7 TPM
Pituitária
24.0 TPM
Brain Frontal Cortex BA9
17.3 TPM
Baço
16.7 TPM
Córtex cerebral
15.3 TPM
OUTRAS DOENÇAS (7)
disabling pansclerotic morphea of childhoodpediatric systemic lupus erythematosusoligoarticular juvenile idiopathic arthritissystemic lupus erythematosus
HGNC:11365UniProt:Q14765
IL2RBInterleukin-2 receptor subunit betaCandidate gene tested inRestrito
FUNÇÃO

Receptor for interleukin-2. This beta subunit is involved in receptor mediated endocytosis and transduces the mitogenic signals of IL2. Probably in association with IL15RA, involved in the stimulation of neutrophil phagocytosis by IL15 (PubMed:15123770, PubMed:31040185)

LOCALIZAÇÃO

Cell membrane

VIAS BIOLÓGICAS (2)
Interleukin-2 signalingInterleukin-15 signaling
MECANISMO DE DOENÇA

Immunodeficiency 63 with lymphoproliferation and autoimmunity

An autosomal recessive disorder characterized by immune dysregulation resulting in lymphoid proliferation, dermatitis, enteropathy, autoantibodies, hypergammaglobulinemia, and immunodeficiency with recurrent infections. Patients show increased susceptibility to viral infections, particularly cytomegalovirus disease.

EXPRESSÃO TECIDUAL(Tecido-específico)
Linfócitos
132.9 TPM
Baço
45.4 TPM
Sangue
24.8 TPM
Pulmão
10.7 TPM
Intestino delgado
8.6 TPM
OUTRAS DOENÇAS (3)
immunodeficiency 63 with lymphoproliferation and autoimmunityoligoarticular juvenile idiopathic arthritisrheumatoid factor-negative juvenile idiopathic arthritis
HGNC:6009UniProt:P14784
CD247T-cell surface glycoprotein CD3 zeta chainCandidate gene tested inModerado
FUNÇÃO

Part of the TCR-CD3 complex present on T-lymphocyte cell surface that plays an essential role in adaptive immune response. When antigen presenting cells (APCs) activate T-cell receptor (TCR), TCR-mediated signals are transmitted across the cell membrane by the CD3 chains CD3D, CD3E, CD3G and CD247/CD3Z. All CD3 chains contain immunoreceptor tyrosine-based activation motifs (ITAMs) in their cytoplasmic domain. Upon TCR engagement, these motifs become phosphorylated by Src family protein tyrosine

LOCALIZAÇÃO

Cell membrane

VIAS BIOLÓGICAS (9)
Translocation of ZAP-70 to Immunological synapseDownstream TCR signalingPhosphorylation of CD3 and TCR zeta chainsImmunoregulatory interactions between a Lymphoid and a non-Lymphoid cellFCGR3A-mediated phagocytosis
MECANISMO DE DOENÇA

Immunodeficiency 25

An immunological deficiency characterized by T-cells impaired immune response to alloantigens, tetanus toxoid and mitogens.

OUTRAS DOENÇAS (4)
immunodeficiency 25rheumatoid factor-negative juvenile idiopathic arthritisT-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zetaoligoarticular juvenile idiopathic arthritis
HGNC:1677UniProt:P20963
ANKRD55Ankyrin repeat domain-containing protein 55Candidate gene tested inTolerante
LOCALIZAÇÃO

OUTRAS DOENÇAS (2)
rheumatoid factor-negative juvenile idiopathic arthritisoligoarticular juvenile idiopathic arthritis
HGNC:25681UniProt:Q3KP44
PTPN2Tyrosine-protein phosphatase non-receptor type 2Candidate gene tested inAltamente restrito
FUNÇÃO

Non-receptor type tyrosine-specific phosphatase that dephosphorylates receptor protein tyrosine kinases including INSR, EGFR, CSF1R, PDGFR. Also dephosphorylates non-receptor protein tyrosine kinases like JAK1, JAK2, JAK3, Src family kinases, STAT1, STAT3 and STAT6 either in the nucleus or the cytoplasm. Negatively regulates numerous signaling pathways and biological processes like hematopoiesis, inflammatory response, cell proliferation and differentiation, and glucose homeostasis. Plays a mult

LOCALIZAÇÃO

Endoplasmic reticulumEndoplasmic reticulum-Golgi intermediate compartmentNucleusCytoplasmCell membrane

VIAS BIOLÓGICAS (1)
Interleukin-37 signaling
EXPRESSÃO TECIDUAL(Ubíquo)
Linfócitos
26.5 TPM
Ovário
21.1 TPM
Pulmão
20.3 TPM
Fibroblastos
19.6 TPM
Baço
19.0 TPM
OUTRAS DOENÇAS (2)
oligoarticular juvenile idiopathic arthritisrheumatoid factor-negative juvenile idiopathic arthritis
HGNC:9650UniProt:P17706
IL2RAInterleukin-2 receptor subunit alphaCandidate gene tested inTolerante
FUNÇÃO

Receptor for interleukin-2. The receptor is involved in the regulation of immune tolerance by controlling regulatory T cells (TREGs) activity. TREGs suppress the activation and expansion of autoreactive T-cells

LOCALIZAÇÃO

Membrane

VIAS BIOLÓGICAS (4)
RAF/MAP kinase cascadeInterleukin receptor SHC signalingInterleukin-2 signalingRUNX1 and FOXP3 control the development of regulatory T lymphocytes (Tregs)
MECANISMO DE DOENÇA

Type 1 diabetes mellitus 10

A multifactorial disorder of glucose homeostasis that is characterized by susceptibility to ketoacidosis in the absence of insulin therapy. Clinical features are polydipsia, polyphagia and polyuria which result from hyperglycemia-induced osmotic diuresis and secondary thirst. These derangements result in long-term complications that affect the eyes, kidneys, nerves, and blood vessels.

EXPRESSÃO TECIDUAL(Tecido-específico)
Baço
9.3 TPM
Linfócitos
8.3 TPM
Intestino delgado
7.2 TPM
Adipose Visceral Omentum
3.0 TPM
Pulmão
2.7 TPM
OUTRAS DOENÇAS (4)
immunodeficiency due to CD25 deficiencyrheumatoid factor-negative juvenile idiopathic arthritisoligoarticular juvenile idiopathic arthritistype 1 diabetes mellitus 10
HGNC:6008UniProt:P01589
PTPN22Tyrosine-protein phosphatase non-receptor type 22Candidate gene tested inTolerante
FUNÇÃO

Acts as a negative regulator of T-cell receptor (TCR) signaling by direct dephosphorylation of the Src family kinases LCK and FYN, ITAMs of the TCRz/CD3 complex, as well as ZAP70, VAV, VCP and other key signaling molecules (PubMed:16461343, PubMed:18056643). Associates with and probably dephosphorylates CBL. Dephosphorylates LCK at its activating 'Tyr-394' residue (PubMed:21719704). Dephosphorylates ZAP70 at its activating 'Tyr-493' residue (PubMed:16461343). Dephosphorylates the immune system a

LOCALIZAÇÃO

Cytoplasm

VIAS BIOLÓGICAS (2)
Phosphorylation of CD3 and TCR zeta chainsTranslocation of ZAP-70 to Immunological synapse
MECANISMO DE DOENÇA

Systemic lupus erythematosus

A chronic, relapsing, inflammatory, and often febrile multisystemic disorder of connective tissue, characterized principally by involvement of the skin, joints, kidneys and serosal membranes. It is of unknown etiology, but is thought to represent a failure of the regulatory mechanisms of the autoimmune system. The disease is marked by a wide range of system dysfunctions, an elevated erythrocyte sedimentation rate, and the formation of LE cells in the blood or bone marrow.

EXPRESSÃO TECIDUAL(Tecido-específico)
Linfócitos
50.6 TPM
Baço
13.9 TPM
Sangue
12.7 TPM
Intestino delgado
9.6 TPM
Pulmão
8.7 TPM
OUTRAS DOENÇAS (6)
systemic lupus erythematosusVogt-Koyanagi-Harada diseaseoligoarticular juvenile idiopathic arthritisrheumatoid factor-negative juvenile idiopathic arthritis
HGNC:9652UniProt:Q9Y2R2

Medicamentos aprovados (FDA)

2 medicamentos encontrados nos registros da FDA americana.

💊 Naproxen (NAPROXEN)
💊 Tofidence (TOCILIZUMAB)
Ver no DailyMed/FDA

Variantes genéticas (ClinVar)

111 variantes patogênicas registradas no ClinVar.

🧬 STAT4: GRCh37/hg19 2q31.3-33.1(chr2:181362315-202911548)x1 ()
🧬 STAT4: NM_003151.4(STAT4):c.372+144C>G ()
🧬 STAT4: NM_003151.4(STAT4):c.2014G>A (p.Gly672Ser) ()
🧬 STAT4: NM_003151.4(STAT4):c.482C>T (p.Thr161Ile) ()
🧬 STAT4: GRCh37/hg19 2q32.1-36.1(chr2:186698504-223918111)x3 ()
Ver todas no ClinVar

Diagnóstico

Os sinais que médicos procuram e os exames que confirmam

Carregando...

Tratamento e manejo

Remédios, cuidados de apoio e o que precisa acompanhar

Pipeline de tratamentos
Pipeline regulatório — de medicamentos já aprovados a drogas em pesquisa exploratória.
Aprovado1
3Fase 39
2Fase 21
1Fase 13
·Pré-clínico4
Medicamentos catalogadosEnsaios clínicos· 0 medicamentos · 18 ensaios
Carregando informações de tratamento...

Onde tratar no SUS

Hospitais de referência no Brasil e o protocolo oficial do SUS (PCDT)

🇧🇷 Atendimento SUS — Poliartrite juvenil

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Selecione um estado ou use sua localização para ver resultados.

Dados de DATASUS/CNES, SBGM, ABNeuro e Ministério da Saúde. Sempre confirme a disponibilidade diretamente com o estabelecimento.

Pesquisa ativa

Ensaios clínicos abertos e novidades científicas recentes

🟢 Recrutando agora

2 pesquisas recrutando participantes. Converse com seu médico sobre a possibilidade de participar.

Outros ensaios clínicos

19 ensaios clínicos encontrados, 2 ativos.

Distribuição por fase
Ver todos no ClinicalTrials.gov
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Publicações mais relevantes

Timeline de publicações
174 papers (10 anos)
#1

Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome without Camptodactyly: A Pediatric Case and Review of the Literature.

Klinische Padiatrie2026 Mar 04

Camptodactyly-arthropathy-coxa vara-pericarditis syndrome is a rare autosomal recessive disorder with camptodactyly, non-inflammatory arthropathy, coxa vara, and pericarditis. Symptoms usually begin in early childhood with swelling of interphalangeal joints, wrists, and knees. Pericarditis is rare. It is caused by proteoglycan 4 gene mutations and often misdiagnosed as juvenile idiopathic arthritis due to overlapping features. A 4-year-old boy presented with 6 months of knee and wrist swelling and nocturnal pain. His parents were first-degree cousins, and a maternal uncle had rheumatoid arthritis. He had prior hip surgeries at 2.5 years. Examination showed swelling in knees, ankles, and wrists, and 30° wrist extension limitation. No systemic symptoms were noted. The erythrocyte sedimentation rate, C-reactive protein level, and antinuclear antibody test results were normal. Magnetic resonance imaging showed effusion and synovial thickening. Initially diagnosed with polyarticular juvenile idiopathic arthritis, he received methotrexate and etanercept. Due to progressive gait issues and radiographic coxa vara, diagnosis was revised. Genetic testing confirmed homozygous proteoglycan 4 (c.915delC) mutation. This case underscores an atypical camptodactyly-arthropathy-coxa vara-pericarditis presentation without camptodactyly. Persistent non-inflammatory arthropathy despite immunosuppression should raise suspicion for camptodactyly-arthropathy-coxa vara-pericarditis. Das Camptodaktylie-Arthropathie-Coxa-vara-Perikarditis (CACP)-Syndrom ist eine seltene autosomal-rezessive Erkrankung, die durch Camptodaktylie, nicht-entzündliche Arthropathie, Coxa vara und Perikarditis gekennzeichnet ist. Die Symptome beginnen typischerweise im frühen Kindesalter mit Schwellungen der Interphalangealgelenke, Handgelenke und Knie. Eine Perikarditis ist selten. Das Syndrom wird durch Mutationen im PRG4-Gen verursacht und aufgrund überlappender klinischer Merkmale häufig mit juveniler idiopathischer Arthritis (JIA) verwechselt.  Ein 4-jähriger Junge stellte sich mit einer sechsmonatigen Vorgeschichte von Schwellungen und nächtlichen Schmerzen in den Knien und Handgelenken vor. Die Eltern waren Cousin und Cousine ersten Grades, ein mütterlicher Onkel hatte rheumatoide Arthritis. Im Alter von 2,5 Jahren hatte der Patient Operationen wegen Hüftdysplasie. Die körperliche Untersuchung ergab Schwellungen in Knien, Sprunggelenken und Handgelenken sowie eine 30°-Streckungseinschränkung in beiden Handgelenken. Systemische Symptome lagen nicht vor. ESR, CRP und ANA waren unauffällig. Die MRT zeigte Gelenkergüsse und synoviale Verdickungen. Zunächst wurde eine polyartikuläre JIA diagnostiziert und mit Methotrexat und später Etanercept behandelt. Aufgrund zunehmender Gangstörungen und radiologischer Zeichen einer Coxa vara wurde die Diagnose überdacht. Eine genetische Analyse bestätigte eine homozygote PRG4-Mutation (c.915delC).  Dieser Fall verdeutlicht eine atypische Präsentation des CACP-Syndroms ohne Camptodaktylie. Eine persistierende, nicht-entzündliche Arthropathie trotz immunsuppressiver Therapie sollte den Verdacht auf ein CACP-Syndrom lenken.

#2

Biologic treatment patterns and challenges in defining difficult-to-treat disease in children with polyarticular juvenile idiopathic arthritis: a real-world study.

Expert opinion on biological therapy2026

To evaluate the clinical characteristics, and treatment patterns of difficult-to-treat (D2T) disease in children with polyarticular juvenile idiopathic arthritis (pJIA) treated with biologic disease-modifying antirheumatic drugs (bDMARDs). This single-center, cross-sectional study included children with RF-positive or RF-negative pJIA who received bDMARD. D2T defined according to EULAR criteria, as inadequate response to at least two bDMARDs with different mechanisms of action. Disease activity was assessed using the JADAS-27. Treatment patterns, switches, and factors associated with D2T were analyzed. A total of 59 pJIA patients (79.9% female) were included, with a median follow-up of 60 months. Ten patients (16.9%) fulfilled the criteria for D2T disease after a follow-up duration of 36 months. At diagnosis, D2T patients had significantly higher inflammatory markers than non-D2T patients, with higher median CRP (45 vs. 12 mg/L, p = 0.002) and ESR (77 vs. 38 mm/h, p = 0.003) values. In univariate analyses, higher CRP, ESR, temporomandibular joint involvement, and higher JADAS-27 at bDMARD initiation were associated with D2T status (p < 0.05). D2T course was associated with temporomandibular joint involvement, elevated inflammatory markers, and higher disease activity at the initiation of the first biologic therapy.

#3

Tocilizumab-induced psoriatic dermatitis in polyarticular juvenile idiopathic arthritis: A rare case report.

SAGE open medical case reports2026

Psoriasis is an immune-mediated inflammatory disorder with a strong genetic predisposition. However, in some cases, it can emerge as an adverse effect of biologic therapy, particularly interleukin-6 inhibitors such as tocilizumab. This case report describes the unexpected onset of psoriatic dermatitis in a 16-year-old male diagnosed with polyarticular juvenile idiopathic arthritis following treatment with tocilizumab. The patient had no prior personal or family history of psoriasis, highlighting a potential paradoxical reaction to interleukin-6 inhibition. Management strategies included topical corticosteroids and vitamin D analogs, with consideration of dose adjustment or transition to an alternative biologic therapy. This case highlights the importance of recognizing dermatologic adverse effects associated with interleukin-6 inhibitors and emphasizes the need for individualized treatment strategies in juvenile idiopathic arthritis patients receiving biologic therapy.

#4

Approval of Upadacitinib in Pediatric Patients with Active Polyarticular Juvenile Idiopathic Arthritis or Active Psoriatic Arthritis: A Regulatory Perspective.

Journal of clinical pharmacology2026 Jan

On April 26, 2024, FDA approved Rinvoq (upadacitinib, extended-release [ER] tablets) and Rinvoq LQ (1 mg/mL oral solution), a new pediatric immediate-release (IR) formulation, for the treatment of active polyarticular juvenile idiopathic arthritis (pJIA) and active psoriatic arthritis (PsA) in patients 2 years of age and older. The approved dosing regimens include a weight-tiered twice daily (BID) regimen with IR oral solution and a once-daily (QD) regimen with ER tablets. The objective of this article is to summarize the FDA's major review findings and considerations supporting these approvals from a regulatory perspective. This clinical development program included a single study (Study 1) conducted in pediatric subjects aged 2 to less than 18 years with JIA with active polyarthritis to evaluate the pharmacokinetics (PK), safety, and tolerability of multiple doses of upadacitinib. No clinical trials or dedicated PK studies were conducted in pediatric patients with PsA. Efficacy was extrapolated from adults with rheumatoid arthritis (RA) or PsA to pediatric patients with pJIA or PsA, respectively, based on a PK-matching approach considering disease similarity, similar response to treatment, and comparable PK exposure. PK data analysis and simulations showed that the approved upadacitinib pediatric dosing regimen, including a BID regimen with IR oral solution and QD regimen with ER tablet, provide comparable PK exposure (Cmax and AUC) in pediatric subjects with pJIA or PsA as compared to the approved 15 mg ER tablet QD regimen in adults with RA or PsA, respectively, supporting the efficacy extrapolation from adults to pediatric subjects.

#5

Real-life data on treatment strategies for polyarticular juvenile idiopathic arthritis.

European journal of pediatrics2025 Sep 30

Polyarticular juvenile idiopathic arthritis (pJIA) is one of the most difficult subgroups of JIA to manage. The aim of this study is to compare patients who were started on MTX at diagnosis and continued on monotherapy during follow-up with patients who later required the addition of bDMARDs. Patients with pJIA following up between January 2013 and December 2023 were included in the study. The juvenile arthritis disease activity score (JADAS) was used for disease activity, and the juvenile arthritis damage index (JADI) was used for damage status. The study included 78 pJIA patients, 56 (71.8%) of whom were girls. The median age at the time of pJIA diagnosis was 11.3 (IQR 6.6-14.3) years. The patients were divided into two groups: those receiving only methotrexate (MTX) (n = 23, 29.5%) and those receiving MTX and biologic disease-modifying anti-rheumatic drugs (bDMARDs) (n = 55, 70.5%). The time elapsed until diagnosis, elbow involvement, duration of follow-up, and time to achieve clinically inactive disease were all significantly higher in patients receiving MTX + bDMARDs (p < 0.05). No significant difference was observed in the JADAS-71 value at diagnosis (p > 0.05). The JADAS-71 and JADI values at the 3rd, 6th, and 12th months were also significantly higher in patients receiving MTX and bDMARDs (p < 0.05). Patients with pJIA can achieve remission with conventional DMARDs alone, such as methotrexate. Patients with high JADAS-71 and JADI-Articular (JADI-A) values may require the use of bDMARDs. In particular, high JADAS-71 values detected at the 6th month can be used as a predictor for starting bDMARDs in pJIA patients. • Polyarticular JIA is a challenging subtype with heterogeneous treatment responses. • Objective tools such as JADAS-71 are widely used to assess disease activity and support treatment monitoring. • JADAS-71 serves as a valuable tool to guide the timing of biologic therapy initiation in pJIA patients. • Although the management of pJIA is challenging for clinicians, some patients may achieve remission with only MTX.

Publicações recentes

Ver todas no PubMed

📚 EuropePMC159 artigos no totalmostrando 161

2026

Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome without Camptodactyly: A Pediatric Case and Review of the Literature.

Klinische Padiatrie
2026

Biologic treatment patterns and challenges in defining difficult-to-treat disease in children with polyarticular juvenile idiopathic arthritis: a real-world study.

Expert opinion on biological therapy
2025

Open-Label Phase II Study of Olokizumab in Adolescent Patients with Polyarticular Juvenile Idiopathic Arthritis: Results of the 24-Week Treatment Period.

Pharmaceuticals (Basel, Switzerland)
2026

Tocilizumab-induced psoriatic dermatitis in polyarticular juvenile idiopathic arthritis: A rare case report.

SAGE open medical case reports
2025

P19 A rare case of PHOAR2-enteropathy syndrome (PHOAR2E; previously known as pachydermoperiostosis) with a causal variant in the SLCO2A1 gene.

The British journal of dermatology
2025

Comparison of clinical practices during the transitional and young adult phases between patients with oligoarticular/polyarticular juvenile idiopathic arthritis and those with rheumatoid arthritis in Japan.

Pediatric rheumatology online journal
2025

Efficacy of biologic DMARDs in improving the clinical response of patients with polyarticular juvenile idiopathic arthritis: a meta-analysis of RCTs.

Advances in rheumatology (London, England)
2025

Real-life data on treatment strategies for polyarticular juvenile idiopathic arthritis.

European journal of pediatrics
2025

CT-P47/Tocilizumab-anoh: A Tocilizumab Biosimilar.

Clinical drug investigation
2026

Approval of Upadacitinib in Pediatric Patients with Active Polyarticular Juvenile Idiopathic Arthritis or Active Psoriatic Arthritis: A Regulatory Perspective.

Journal of clinical pharmacology
2025

Telemedicine for paediatric rheumatic diseases in Japan: a national survey of physicians' perspectives.

Modern rheumatology
2025

Rare coexistence of X-linked hyper immunoglobulin M syndrome and polyarticular juvenile idiopathic arthritis in a Chinese child: A case report.

Joint diseases and related surgery
2025

Model-Informed Paradigm in Drug Development-An End-To-End Case Study From Upadacitinib Development.

Clinical and translational science
2025

Treatment of polyarticular juvenile idiopathic arthritis in Latin America: recommendations from the Pan-American League of Associations for Rheumatology.

The Lancet. Child &amp; adolescent health
2025

Inflammation-induced leg length discrepancy in children: from molecular mechanisms to clinical implications.

Frontiers in medicine
2025

Three-Year Outcomes and Latent Class Trajectory Analysis of the Childhood Arthritis and Rheumatology Research Alliance Polyarticular JIA Consensus Treatment Plans Study.

Arthritis &amp; rheumatology (Hoboken, N.J.)
2025

Comparative efficacy and safety of etanercept and adalimumab in the treatment of polyarticular juvenile idiopathic arthritis.

BMC pediatrics
2025

Clinical insights into heterogeneity of rheumatoid factor negative polyarticular juvenile idiopathic arthritis across the world.

Pediatric rheumatology online journal
2025

African guidelines for diagnosis and management of polyarticular juvenile idiopathic arthritis: PAFLAR initiative.

Pediatric rheumatology online journal
2025

Using genetics, genomics, and transcriptomics to identify therapeutic targets in juvenile idiopathic arthritis.

HGG advances
2025

An update on the safety of biologic therapies for the treatment of polyarticular juvenile idiopathic arthritis.

Expert opinion on drug safety
2025

Experience with upadacitinib in refractory polyarticular juvenile idiopathic arthritis.

Rheumatology (Oxford, England)
2025

Characteristics of refractory disease and persistent symptoms in inflammatory arthritis: Qualitative framework analysis of interviews with patients and health care professionals.

British journal of health psychology
2025

Identification and validation of susceptibility modules and hub genes in polyarticular juvenile idiopathic arthritis using WGCNA and machine learning.

Autoimmunity
2025

Polyarticular juvenile idiopathic arthritis with Madelung deformity and arthritis mutilans in 18p deletion syndrome.

Rheumatology (Oxford, England)
2024

Intraarticular corticosteroid injections in pediatric rheumatology: insights from specialists.

European journal of pediatrics
2024

Increased neutrophil extracellular trap formation in oligoarticular, polyarticular juvenile idiopathic arthritis and enthesitis-related arthritis: biomarkers for diagnosis and disease activity.

Frontiers in immunology
2024

Genetic Mutations Associated With TNFAIP3 (A20) Haploinsufficiency and Their Impact on Inflammatory Diseases.

International journal of molecular sciences
2024

Functional status of Indian children with juvenile idiopathic arthritis.

Rheumatology and immunology research
2024

Uveitis as predictor of disease flare after the first anti-TNF withdrawal in oligoarticular and polyarticular juvenile idiopathic arthritis: a multicentric Italian experience.

Clinical and experimental rheumatology
2024

Treatment Patterns in Polyarticular Juvenile Idiopathic Arthritis: A Retrospective Observational Health Claims Data Study.

Life (Basel, Switzerland)
2024

S100 proteins as potential predictive biomarkers of abatacept response in polyarticular juvenile idiopathic arthritis.

Arthritis research &amp; therapy
2024

Transcriptomic signatures of classical monocytes reveal pro-inflammatory modules and heterogeneity in polyarticular juvenile idiopathic arthritis.

Frontiers in immunology
2024

Polyarticular juvenile idiopathic arthritis with rice bodies formation: A case report.

International journal of rheumatic diseases
2025

Polyarticular juvenile idiopathic arthritis has a distinct co-inhibitor receptor profile.

Rheumatology (Oxford, England)
2024

Loeffler's Endocarditis- A cause of endomyocardial fibrosis in a patient of juvenile idiopathic arthritis: A Case Report.

JPMA. The Journal of the Pakistan Medical Association
2024

Th17/1 and ex-Th17 cells are detected in patients with polyarticular juvenile arthritis and increase following treatment.

Pediatric rheumatology online journal
2024

[Protocols in pediatric rheumatology (PROKIND): treat-to-target in polyarticular juvenile idiopathic arthritis].

Zeitschrift fur Rheumatologie
2024

Potential Process Control Issues With Abatacept.

Contact in context
2023

Risk of flare in juvenile idiopathic arthritis: Is it related to the methotrexate treatment strategy or patient characteristics?

Archives of rheumatology
2023

Identification of key biomarkers in RF-negative polyarticular and oligoarticular juvenile idiopathic arthritis by bioinformatic analysis.

Pediatric rheumatology online journal
2023

Interleukin 6: at the interface of human health and disease.

Frontiers in immunology
2023

Children with extended oligoarticular and polyarticular juvenile idiopathic arthritis have alterations in B and T follicular cell subsets in peripheral blood and a cytokine profile sustaining B cell activation.

RMD open
2023

Bone erosions associated with systemic bone loss on HR-pQCT in women with longstanding polyarticular juvenile idiopathic arthritis.

Seminars in arthritis and rheumatism
2023

Refractory inflammatory arthritis definition and model generated through patient and multi-disciplinary professional modified Delphi process.

PloS one
2023

Golimumab for Polyarticular Juvenile Idiopathic Arthritis and Psoriatic Arthritis: Pharmacologic and Clinical Considerations.

Life (Basel, Switzerland)
2023

Bradycardia after pulse methylprednisolone therapy in a child-Uncommon side effect of a frequently used drug: A case report.

Journal of family medicine and primary care
2023

Baricitinib in juvenile idiopathic arthritis: an international, phase 3, randomised, double-blind, placebo-controlled, withdrawal, efficacy, and safety trial.

Lancet (London, England)
2023

Childhood-Onset COPA Syndrome Recognized Retrospectively in the Context of Polyarticular Juvenile Idiopathic Arthritis and Rheumatoid Arthritis.

Case reports in rheumatology
2023

Microscopic Polyangiitis with Pulmonary-renal Involvement in a Patient with Polyarticular Juvenile Idiopathic Arthritis: A Case Report.

Indian journal of nephrology
2023

Factors associated with medication adherence among children with rheumatic diseases.

Frontiers in pharmacology
2023

Therapeutic Development in Polyarticular Course Juvenile Idiopathic Arthritis: Extrapolation, Dose Selection, and Clinical Trial Design.

Arthritis &amp; rheumatology (Hoboken, N.J.)
2023

Study of the shared gene signatures of polyarticular juvenile idiopathic arthritis and autoimmune uveitis.

Frontiers in immunology
2023

Population Pharmacokinetics and Exposure-Response Modeling Analyses of Golimumab in Children and Young Adults With Recently Diagnosed Type 1 Diabetes.

Journal of clinical pharmacology
2023

Dry synovitis, a rare entity distinct from juvenile idiopathic arthritis.

Pediatric rheumatology online journal
2023

Investigating Wrist Joint Position Sense and Hand Functions in Children With Polyarticular Juvenile Idiopathic Arthritis With Wrist Involvement.

Clinical pediatrics
2023

Risk stratification using anti-citrullinated peptide antibodies (ACPA) in polyarticular subtypes of juvenile idiopathic arthritis in adulthood.

Joint bone spine
2023

Aqua-Plyometric Exercises-Induced Changes in Muscle Strength, Bone Mineral Properties, and Physical Fitness in Patients With Juvenile Idiopathic Arthritis: A 12-Week, Randomized Controlled Trial.

Pediatric exercise science
2022

Economic evaluation of infliximab, synthetic triple therapy and methotrexate in the treatment of newly diagnosed juvenile idiopathic arthritis.

Pediatric rheumatology online journal
2023

Biologics with or without methotrexate in treatment of polyarticular juvenile idiopathic arthritis: effectiveness, safety and drug survival.

Rheumatology (Oxford, England)
2022

Intravenous Golimumab in Patients with Polyarticular Juvenile Idiopathic Arthritis and Juvenile Psoriatic Arthritis and Subcutaneous Ustekinumab in Patients with Juvenile Psoriatic Arthritis: Extrapolation of Data from Studies in Adults and Adjacent Pediatric Populations.

Paediatric drugs
2023

Atypical polyarticular juvenile idiopathic arthritis revealing multicentric reticulohistiocytosis with pulmonary involvement.

Rheumatology (Oxford, England)
2022

α2-fraction and haptoglobin as biomarkers for disease activity in oligo- and polyarticular juvenile idiopathic arthritis.

Pediatric rheumatology online journal
2022

Oral or Parenteral Methotrexate for the Treatment of Polyarticular Juvenile Idiopathic Arthritis.

European journal of rheumatology
2022

Impact of Clinical Pilates Exercise on Pain, Cardiorespiratory Fitness, Functional Ability, and Quality of Life in Children with Polyarticular Juvenile Idiopathic Arthritis.

International journal of environmental research and public health
2022

The Association Between the Use of Low-Slice Computed Tomography Machines and Downstream Care: Comparative Study of 16-Slice and 64-Slice Computed Tomography Angiography.

JMIR formative research
2022

Mitigated suppressive function of regulatory T cells (Treg) upon Th17-inducing cytokines in oligo- and polyarticular Juvenile Idiopathic Arthritis (JIA) patients.

Pediatric rheumatology online journal
2022

Social determinants of health influence disease activity and functional disability in Polyarticular Juvenile Idiopathic Arthritis.

Pediatric rheumatology online journal
2022

Efficacy of tocilizumab for interstitial lung disease associated with polyarticular juvenile idiopathic arthritis.

Pediatrics international : official journal of the Japan Pediatric Society
2022

[Polyarticular juvenile idiopathic arthritis and rheumatoid arthritis : Common features and differences].

Zeitschrift fur Rheumatologie
2022

Low-energy laser therapy application on knee joints as an auxiliary treatment in patients with polyarticular juvenile idiopathic arthritis: a dual-arm randomized clinical trial.

Lasers in medical science
2021

Subcutaneous golimumab induced and maintained clinical response in a child with a biological-experienced steroid-refractory flare of ulcerative colitis: A case report.

Medicine
2021

Interstitial lung disease occurring shortly after tocilizumab infusion in a patient with polyarticular juvenile idiopathic arthritis: a case report.

Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology
2021

Community poverty level influences time to first pediatric rheumatology appointment in Polyarticular Juvenile Idiopathic Arthritis.

Pediatric rheumatology online journal
2021

A case report of intracranial hypertension and aseptic meningitis: anti-tumor necrosis factor associated or juvenile idiopathic arthritis related.

The Turkish journal of pediatrics
2021

Juvenile Idiopathic Arthritis-Associated Chronic Uveitis: Recent Therapeutic Approaches.

Journal of clinical medicine
2021

The value of the patient global health assessment in polyarticular juvenile idiopathic arthritis: a nested cohort study.

Journal of patient-reported outcomes
2021

Optimizing the Start Time of Biologics in Polyarticular Juvenile Idiopathic Arthritis: A Comparative Effectiveness Study of Childhood Arthritis and Rheumatology Research Alliance Consensus Treatment Plans.

Arthritis &amp; rheumatology (Hoboken, N.J.)
2021

Improved Disease Course Associated With Early Initiation of Biologics in Polyarticular Juvenile Idiopathic Arthritis: Trajectory Analysis of a Childhood Arthritis and Rheumatology Research Alliance Consensus Treatment Plans Study.

Arthritis &amp; rheumatology (Hoboken, N.J.)
2021

Disseminated coccidioidomycosis in a patient with juvenile idiopathic arthritis receiving infliximab.

Pediatric rheumatology online journal
2021

[Cushing's syndrome with subsequent tertiary adrenocortical insufficiency after simultaneous multiple intra-articular local glucocorticoid treatment : Keep an eye on hormone deficiency conditions requiring treatment after multiple administrations of local steroids].

Zeitschrift fur Rheumatologie
2021

Rheumatoid factor positive polyarticular juvenile idiopathic arthritis associated with a novel COPA mutation.

Rheumatology (Oxford, England)
2021

Summarizing current refractory disease definitions in rheumatoid arthritis and polyarticular juvenile idiopathic arthritis: systematic review.

Rheumatology (Oxford, England)
2021

Underlying CTLA4 Deficiency in a Patient With Juvenile Idiopathic Arthritis and Autoimmune Lymphoproliferative Syndrome Features Successfully Treated With Abatacept-A Case Report.

Journal of pediatric hematology/oncology
2021

Subcutaneous dosing regimens of tocilizumab in children with systemic or polyarticular juvenile idiopathic arthritis.

Rheumatology (Oxford, England)
2021

Concentration of survivin in children with oligo- and polyarticular juvenile idiopathic arthritis (JIA): diagnostic and prognostic value-a single-center study.

Arthritis research &amp; therapy
2021

Open-label phase 3 study of intravenous golimumab in patients with polyarticular juvenile idiopathic arthritis.

Rheumatology (Oxford, England)
2020

Peripheral Blood Lymphocyte Analysis in Oligo- and Polyarticular Juvenile Idiopathic Arthritis Patients Receiving Methotrexate or Adalimumab Therapy: A Cross-Sectional Study.

Frontiers in pediatrics
2021

Model-Based Selection and Recommendation for Subcutaneous Abatacept Dose in Patients With Polyarticular Juvenile Idiopathic Arthritis.

Journal of clinical pharmacology
2021

Fallen, But Not Forgotten: Atlantoaxial Dislocation in a Child With Polyarticular Juvenile Idiopathic Arthritis in the Era of Biologics.

Journal of clinical rheumatology : practical reports on rheumatic &amp; musculoskeletal diseases
2020

Longitudinal assessment of racial disparities in juvenile idiopathic arthritis disease activity in a treat-to-target intervention.

Pediatric rheumatology online journal
2021

Platelet Glycoprotein Ib α-Chain as a Putative Therapeutic Target for Juvenile Idiopathic Arthritis: A Mendelian Randomization Study.

Arthritis &amp; rheumatology (Hoboken, N.J.)
2020

Coexistence of a novel WISP3 pathogenic variant and an MEFV mutation in an Arabic family with progressive pseudorheumatoid dysplasia mimicking polyarticular juvenile idiopathic arthritis.

Pediatric rheumatology online journal
2020

Long-term outcomes in patients with polyarticular juvenile idiopathic arthritis receiving adalimumab with or without methotrexate.

RMD open
2021

Impact of core stability exercises on bone mineralization and functional capacity in children with polyarticular juvenile idiopathic arthritis: a randomized clinical trial.

Clinical rheumatology
2020

Type 1 interferonopathy presenting as juvenile idiopathic arthritis with interstitial lung disease: report of a new phenotype.

Pediatric rheumatology online journal
2020

Treat-to-target study for improved outcome in polyarticular juvenile idiopathic arthritis.

Annals of the rheumatic diseases
2020

PADI4 (rs2240340), PDCD1 (rs10204525), and CTLA4 (231775) gene polymorphisms and polyarticular juvenile idiopathic arthritis.

British journal of biomedical science
2019

Pediatric mesenteric panniculitis: three cases and a review of the literature.

The Turkish journal of pediatrics
2021

Low Incidence of Inflammatory Bowel Disease Adverse Events in Adalimumab Clinical Trials Across Nine Different Diseases.

Arthritis care &amp; research
2020

Biologic Therapies in Polyarticular Juvenile Idiopathic Arthritis. Comparison of Long-Term Safety Data from the German BIKER Registry.

ACR open rheumatology
2019

Arthritis in children with LRBA deficiency - case report and literature review.

Pediatric rheumatology online journal
2019

Health-related quality of life during early aggressive treatment in patients with polyarticular juvenile idiopathic arthritis: results from randomized controlled trial.

Pediatric rheumatology online journal
2020

Infliximab therapy and outcomes in patients with polyarticular juvenile idiopathic arthritis: a single-center study in China.

World journal of pediatrics : WJP
2019

Canakinumab in Children with Familial Mediterranean Fever: A Single-Center, Retrospective Analysis.

Paediatric drugs
2020

Efficacy and safety of tocilizumab in a real-life observational cohort of patients with polyarticular juvenile idiopathic arthritis.

Rheumatology (Oxford, England)
2020

Outcome Monitoring and Clinical Decision Support in Polyarticular Juvenile Idiopathic Arthritis.

The Journal of rheumatology
2019

Expanding the spectrum of A20 haploinsufficiency in two Chinese families: cases report.

BMC medical genetics
2019

Slow speed resistance exercise training in children with polyarticular juvenile idiopathic arthritis.

Open access rheumatology : research and reviews
2019

[Biologics in the treatment of juvenile idiopathic arthritis : A comparison of mono- and combination therapy with synthetic DMARDs].

Zeitschrift fur Rheumatologie
2019

Biallelic loss-of-function LACC1/FAMIN Mutations Presenting as Rheumatoid Factor-Negative Polyarticular Juvenile Idiopathic Arthritis.

Scientific reports
2019

Population Pharmacokinetics and Exposure-Response Modeling Analyses of Golimumab in Children With Moderately to Severely Active Ulcerative Colitis.

Journal of clinical pharmacology
2019

Physical Fitness in Patients With Oligoarticular and Polyarticular Juvenile Idiopathic Arthritis Diagnosed in the Era of Biologics: A Controlled Cross-Sectional Study.

Arthritis care &amp; research
2020

Height and sexual maturation in girls with juvenile idiopathic arthritis.

Jornal de pediatria
2018

Physical activity in patients with oligo- and polyarticular juvenile idiopathic arthritis diagnosed in the era of biologics: a controlled cross-sectional study.

Pediatric rheumatology online journal
2018

The First Report of Multicentric Carpotarsal Osteolysis Syndrome Caused by MAFB Mutation in Asian.

Case reports in medicine
2018

SB5: An Adalimumab Biosimilar.

BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy
2018

Identification of enhanced IFN-γ signaling in polyarticular juvenile idiopathic arthritis with mass cytometry.

JCI insight
2018

Safety of Adalimumab in Pediatric Patients with Polyarticular Juvenile Idiopathic Arthritis, Enthesitis-Related Arthritis, Psoriasis, and Crohn's Disease.

The Journal of pediatrics
2019

PAIN PERCEPTION AND PAIN COPING MECHANISMS IN CHILDREN AND ADOLESCENTS WITH JUVENILE FIBROMYALGIA AND POLYARTICULAR JUVENILE IDIOPATHIC ARTHRITIS.

Revista paulista de pediatria : orgao oficial da Sociedade de Pediatria de Sao Paulo
2019

Comparison of Adults With Polyarticular Juvenile Idiopathic Arthritis to Adults With Rheumatoid Arthritis: A Cross-sectional Analysis of Clinical Features and Medication Use.

Journal of clinical rheumatology : practical reports on rheumatic &amp; musculoskeletal diseases
2018

Bilateral absence of the cruciate ligaments with meniscal dysplasia: Unexpected diagnosis in a child with juvenile idiopathic arthritis.

Clinical imaging
2018

Is palindromic rheumatism amongst children a benign disease?

Pediatric rheumatology online journal
2018

Brief Report: The Genetic Profile of Rheumatoid Factor-Positive Polyarticular Juvenile Idiopathic Arthritis Resembles That of Adult Rheumatoid Arthritis.

Arthritis &amp; rheumatology (Hoboken, N.J.)
2018

Switched Memory B Cells Are Increased in Oligoarticular and Polyarticular Juvenile Idiopathic Arthritis and Their Change Over Time Is Related to Response to Tumor Necrosis Factor Inhibitors.

Arthritis &amp; rheumatology (Hoboken, N.J.)
2018

Prior to extension, Transcriptomes of fibroblast-like Synoviocytes from extended and Polyarticular juvenile idiopathic arthritis are indistinguishable.

Pediatric rheumatology online journal
2018

Early prediction for over two years efficacy of the first biologic agent for polyarticular juvenile idiopathic arthritis: A multi-institutional study in Japan.

Modern rheumatology
2018

High Levels of DEK Autoantibodies in Sera of Patients With Polyarticular Juvenile Idiopathic Arthritis and With Early Disease Flares Following Cessation of Anti-Tumor Necrosis Factor Therapy.

Arthritis &amp; rheumatology (Hoboken, N.J.)
2018

Adiposity in Juvenile Psoriatic Arthritis.

The Journal of rheumatology
2017

Predictors of methotrexate response in Turkish children with oligoarticular and polyarticular juvenile idiopathic arthritis.

The Turkish journal of pediatrics
2017

Protocols on classification, monitoring and therapy in children's rheumatology (PRO-KIND): results of the working group Polyarticular juvenile idiopathic arthritis.

Pediatric rheumatology online journal
2017

Spontaneous regression of Epstein-Barr virus-associated lymphoproliferative disorder in a juvenile idiopathic arthritis patient after the discontinuation of methotrexate and etanercept.

European journal of rheumatology
2017

Golimumab: A Review in Inflammatory Arthritis.

BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy
2017

Juvenile Idiopathic Arthritis.

Balkan medical journal
2018

Plasma exchange successfully treated macrophage activation syndrome in rheumatoid factor-positive polyarticular juvenile idiopathic arthritis with co-existing pneumonia.

International journal of rheumatic diseases
2017

Safety of tocilizumab in the treatment of juvenile idiopathic arthritis.

Expert opinion on drug safety
2016

Biological agents in polyarticular juvenile idiopathic arthritis: A meta-analysis of randomized withdrawal trials.

Seminars in arthritis and rheumatism
2017

Pathway analysis based on Monte Carlo Cross-Validation in polyarticular juvenile idiopathic arthritis.

Pathology, research and practice
2016

Comparison of treatment response, remission rate and drug adherence in polyarticular juvenile idiopathic arthritis patients treated with etanercept, adalimumab or tocilizumab.

Arthritis research &amp; therapy
2016

A Novel Method for Pathway Identification Based on Attractor and Crosstalk in Polyarticular Juvenile Idiopathic Arthritis.

Medical science monitor : international medical journal of experimental and clinical research
2017

Interleukin-33 as a marker of disease activity in rheumatoid factor positive polyarticular juvenile idiopathic arthritis.

Modern rheumatology
2016

Cost-Effectiveness Analysis of First-Line Treatment With Biologic Agents in Polyarticular Juvenile Idiopathic Arthritis.

Arthritis care &amp; research
2016

Safety and efficacy of etanercept and adalimumab in children aged 2 to 4 years with juvenile idiopathic arthritis.

Clinical rheumatology
2016

Multifocal pigmented villonodular synovitis in a child: A case report.

Medicine
2017

No association between vitamin D levels around time of birth and later risk of developing oligo- and polyarticular juvenile idiopathic arthritis: a Danish case-cohort study.

Scandinavian journal of rheumatology
2016

Proceedings of the 2016 Childhood Arthritis and Rheumatology Research Alliance (CARRA) Scientific Meeting : Toronto, Canada. 14-17 April 2016.

Pediatric rheumatology online journal
2016

Whole blood expression profiling from the TREAT trial: insights for the pathogenesis of polyarticular juvenile idiopathic arthritis.

Arthritis research &amp; therapy
2017

Monitoring of Epstein-Barr virus load and killer T cells in patients with juvenile idiopathic arthritis treated with methotrexate or tocilizumab.

Modern rheumatology
2016

Palisaded Neutrophilic Granulomatous Dermatitis in a Child with Juvenile Idiopathic Arthritis on Etanercept.

Pediatric dermatology
2016

A novel reactive epitope-based antigen targeted by serum autoantibodies in oligoarticular and polyarticular juvenile idiopathic arthritis and development of an electrochemical biosensor.

Immunobiology
2016

Adalimumab in pediatric Crohn's disease.

Immunotherapy
2016

Juvenile arthritis disease activity score is a better reflector of active disease than the disease activity score 28 in adults with polyarticular juvenile idiopathic arthritis.

Annals of the rheumatic diseases
2016

Prediction of long-term remission of oligo/polyarticular juvenile idiopathic arthritis with S100A12 and vascular endothelial growth factor.

Modern rheumatology
2016

Disease activity score in 28 joints at 3 months after the initiation of biologic agent can be a predictive target for switching to the second biologic agent in patients with polyarticular juvenile idiopathic arthritis.

Modern rheumatology
2015

Advances in the treatment of polyarticular juvenile idiopathic arthritis.

Current opinion in rheumatology
2016

Effects of Combined Resistive Underwater Exercises and Interferential Current Therapy in Patients with Juvenile Idiopathic Arthritis: A Randomized Controlled Trial.

American journal of physical medicine &amp; rehabilitation
2016

A new alternative therapy in dermatology: tocilizumab.

Cutaneous and ocular toxicology
2015

Association between cannabinoid receptor type 2 Q63R variant and oligo/polyarticular juvenile idiopathic arthritis.

Scandinavian journal of rheumatology
2016

Long-term safety of etanercept and adalimumab compared to methotrexate in patients with juvenile idiopathic arthritis (JIA).

Annals of the rheumatic diseases
2015

Radiological improvement by tocilizumab in polyarticular juvenile idiopathic arthritis.

Pediatrics international : official journal of the Japan Pediatric Society
2015

X-linked agammaglobulinemia in two siblings with a novel mutation in the BTK gene who presented with polyarticular juvenile idiopathic arthritis.

Scandinavian journal of rheumatology

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Referências e fontes

Bases de dados externas citadas neste artigo

Publicações científicas

Artigos indexados no PubMed ligados a esta doença no grafo RarasNet — título, periódico e PMID direto da fonte, sem intermediação de IA.

  1. Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome without Camptodactyly: A Pediatric Case and Review of the Literature.
    Klinische Padiatrie· 2026· PMID 41780543mais citado
  2. Biologic treatment patterns and challenges in defining difficult-to-treat disease in children with polyarticular juvenile idiopathic arthritis: a real-world study.
    Expert opinion on biological therapy· 2026· PMID 41723586mais citado
  3. Tocilizumab-induced psoriatic dermatitis in polyarticular juvenile idiopathic arthritis: A rare case report.
    SAGE open medical case reports· 2026· PMID 41523326mais citado
  4. Approval of Upadacitinib in Pediatric Patients with Active Polyarticular Juvenile Idiopathic Arthritis or Active Psoriatic Arthritis: A Regulatory Perspective.
    Journal of clinical pharmacology· 2026· PMID 41014542mais citado
  5. Real-life data on treatment strategies for polyarticular juvenile idiopathic arthritis.
    European journal of pediatrics· 2025· PMID 41026294mais citado
  6. [Clinical characteristics and outcomes analysis of children with rheumatoid factor-positive polyarticular juvenile idiopathic arthritis].
    Zhejiang Da Xue Xue Bao Yi Xue Ban· 2026· PMID 41974575recente
  7. Status and progress in the development of rDNA-derived Tocilizumab and its biosimilars for treatment of rheumatoid arthritis.
    Biologicals· 2026· PMID 41895033recente
  8. A Case of Refractory Polyarticular Juvenile Idiopathic Arthritis Post-hematopoietic Stem Cell Transplantation Successfully Treated With Ruxolitinib.
    Cureus· 2026· PMID 41883911recente

Bases de dados e fontes oficiais

Identificadores e referências canônicas usadas para montar este verbete.

  1. ORPHA:404580(Orphanet)
  2. MONDO:0018456(MONDO)
  3. GARD:21729(GARD (NIH))
  4. Variantes catalogadas(ClinVar)
  5. Busca completa no PubMed(PubMed)
  6. Q56014153(Wikidata)

Dados compilados pelo RarasNet a partir de fontes abertas (Orphanet, OMIM, MONDO, PubMed/EuropePMC, ClinicalTrials.gov, DATASUS, PCDT/MS). Este conteúdo é informativo e não substitui avaliação médica.

Conteúdo mantido por Agente Raras · Médicos e pesquisadores podem colaborar

Poliartrite juvenil
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Poliartrite juvenil

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