Follicular Becker's Nevus: Clinical, Dermoscopic and Histopathological Description of Two Cases and Literature Review.

GLUT1DS: focus on motor profile.

Transcriptomic profiling reveals RetS-mediated regulation of type VI secretion system and host cell responses in Pseudomonas aeruginosa infections.

Enteropathogenic Escherichia coli revisited - New insights into old EPEC isolates using whole genome sequencing.

Molecular Characterization of a Rare ESBL E. coli Strain Causing a Necrotizing Enterocolitis Outbreak in Preterm Infants.

Multiple Cutaneous Leiomyomas of the Shoulder: Investigating Chronic Pain and Reed's Syndrome Association.

Uncovering a Novel Pathogenic Mechanism of BCS1L in Mitochondrial Disorders: Insights from Functional Studies on the c.38A>G Variant.

Virtual Reality as a Tool for Upper Limb Rehabilitation in Rett Syndrome: Reducing Stereotypies and Improving Motor Skills.

Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity.

Pathophysiological Significance of α-Synuclein in Sympathetic Nerves: In Vivo Observations.

Videodermoscopy as a Diagnostic Tool for Pili Trianguli and Canaliculi Syndrome.

Nonmodifiable Risk Factors Predict Outcomes in Brugada Syndrome.

Dermoscopic Features of Pili Annulati: Features of PA.

Takotsubo syndrome in a Sardinian amyotrophic lateral sclerosis cohort.

Forecasting potential invaders to prevent future biological invasions worldwide.

Trichoscopic findings in neonatal alopecia in oro-facial-digital syndrome type 1.

Hair Evaluation in Orthodontic Patients with Oligodontia.

Hereditary Leiomyomatosis and Renal Cell Cancer: A Case Report of Pilar Leiomyomatosis with History of Kidney Cancer and Review of the Literature.

Cochlear implantation in Bjornstad syndrome: a case series with literature review.

Compositional and functional aberrance of the gut microbiota in treatment-naïve patients with primary Sjögren's syndrome.

Amuc attenuates high-fat diet-induced metabolic disorders linked to the regulation of fatty acid metabolism, bile acid metabolism, and the gut microbiota in mice.

Overall Survival and Updated Results for Sunitinib Compared With Interferon Alfa in Patients With Metastatic Renal Cell Carcinoma.

Family and Caregiver Characteristics Contribute to Caregiver Change in Use of Strategies and Growth in Child Spoken Language in a Parent-Implemented Language Intervention in Fragile X Syndrome.

Evaluation of hair structural abnormalities in children with different neurological diseases.

Post-intubation laryngeal injury after COVID-19 treatment causing dyspnea: A report of six cases.

Compositional and functional aberrance of the gut microbiota in treatment naïve patients with primary Sjögren's syndrome.

Concealed Substrates in Brugada Syndrome: Isolated Channelopathy or Associated Cardiomyopathy?

Diabetes Affects Antibody Response to SARS-CoV-2 Vaccination in Older Residents of Long-term Care Facilities: Data From the GeroCovid Vax Study.

Identification of two novel variants of BCS1L gene in a patient with classical GRACILE syndrome.

Characterization of enterohemorrhagic Escherichia coli from diarrhoeic patients with particular reference to production of Shiga-like toxin.

Pili Torti: A Feature of Numerous Congenital and Acquired Conditions.

Genetics, Structure, and Function of Group A Streptococcal Pili.

Leiomyosarcoma of the vulva: a case report.

Multi-segmental postural control patterns in down syndrome.

Horizontally acquired papGII-containing pathogenicity islands underlie the emergence of invasive uropathogenic Escherichia coli lineages.

A novel mutation in the ubiquinol-cytochrome c reductase synthesis-like gene associated with complex III deficiency and Björnstad syndrome: A case report.

Clinical, trichoscopy, and light microscopic findings in hypohidrotic ectodermal dysplasia: Report of 21 patients and a review of the literature.

A New Splice-site Mutation of SPINK5 Gene in the Netherton Syndrome with Different Clinical Features: A Case Report.

Cutaneous Leiomyoma Mimicking a Keloid.

Hair cross-sectioning in uncombable hair syndrome: An epoxy embedding technique.

Visual Dermatology: Menkes Disease.

Characterization of native Escherichia coli populations from bovine vagina of healthy heifers and cows with postpartum uterine disease.

Pili trianguli et canaliculi as a phenotypic subtype in patients with central centrifugal cicatricial alopecia: A scanning electron microscopy study.

Controlled trial of lovastatin combined with an open-label treatment of a parent-implemented language intervention in youth with fragile X syndrome.

Expression and Functional Characterization of Various Chaperon-Usher Fimbriae, Curli Fimbriae, and Type 4 Pili of Enterohemorrhagic Escherichia coli O157:H7 Sakai.

Clouston syndrome with pili canaliculi, pili torti, overgrown hyponychium, onycholysis, taurodontism and absence of palmoplantar keratoderma.

Diagnosis of pili trianguli et canaliculi by frozen section: A rapid and inexpensive method of diagnosis.

Nevus psiloliparus: Newly described histopathological features from transverse sections.

The autonomic innervation of hairy skin in humans: an in vivo confocal study.

Association of innervation-adjusted alpha-synuclein in arrector pili muscles with cardiac noradrenergic deficiency in autonomic synucleinopathies.

An unusual pacing artifact.

Large-scale genome analysis of bovine commensal Escherichia coli reveals that bovine-adapted E. coli lineages are serving as evolutionary sources of the emergence of human intestinal pathogenic strains.

Molecular genetic investigations identify new clinical phenotypes associated with BCS1L-related mitochondrial disease.

QseC Signaling in the Outbreak O104:H4 Escherichia coli Strain Combines Multiple Factors during Infection.

Spontaneous Quick Resolution of Uncombable Hair Syndrome-Like Disease.

A 'pathogenic needle' in a 'commensal haystack': Genetic virulence signatures of Corynebacterium glucuronolyticum that may drive its infectious propensity for the male urogenital system.

The potential probiotic Lactobacillus rhamnosus CNCM I-3690 strain protects the intestinal barrier by stimulating both mucus production and cytoprotective response.

Hazard Identification and Characterization: Criteria for Categorizing Shiga Toxin-Producing Escherichia coli on a Risk Basis†.

Clinical spectrum of BCS1L Mitopathies and their underlying structural relationships.

Improving hazard characterization in microbial risk assessment using next generation sequencing data and machine learning: Predicting clinical outcomes in shigatoxigenic Escherichia coli.

Trichoscopy in Hair Shaft Disorders.

Characterization of a novel plasmid encoding F4-like fimbriae present in a Shiga-toxin producing enterotoxigenic Escherichia coli isolated during the investigation on a case of hemolytic-uremic syndrome.

Comparative Transcriptome Profiling Reveals a Potential Role of Type VI Secretion System and Fimbriae in Virulence of Non-O157 Shiga Toxin-Producing Escherichia coli.

Hair cross-sectioning in uncombable hair syndrome: An easy tool for complex diagnosis.

Cutaneous Smooth Muscle Tumors: A Review.

An ADAM-10 dependent EPCR shedding links meningococcal interaction with endothelial cells to purpura fulminans.

Metformin associated lactic acidosis: a case series of 28 patients treated with sustained low-efficiency dialysis (SLED) and long-term follow-up.

Pili torti, pale and elastic skin, and severe neurological impairment.

A novel homozygous mutation in PVRL4 causes ectodermal dysplasia-syndactyly syndrome 1.

Pili annulati in a case of Rothmund-Thomson syndrome with a novel frameshift mutation in RECQL4.

Multiplex real-time PCR assay for detection of Escherichia coli O157:H7 and screening for non-O157 Shiga toxin-producing E. coli.

Patients with a new variant of endemic pemphigus foliaceus have autoantibodies against arrector pili muscle, colocalizing with MYZAP, p0071, desmoplakins 1 and 2 and ARVCF.

Genome sequencing and comparative genomics of enterohemorrhagic Escherichia coli O145:H25 and O145:H28 reveal distinct evolutionary paths and marked variations in traits associated with virulence & colonization.

Xylella fastidiosa: an examination of a re-emerging plant pathogen.

Novel compound heterozygous mutations in BCS1L gene causing Bjornstad syndrome in two siblings.

A review on strategies for decreasing E. coli O157:H7 risk in animals.

THE STRUCTURE OF THE INTESTINAL MICROBIOTA AND THE FREQUENCY OF DETECTION OF PATHOGENICITY GENES (STXI, STX2, BFP) IN ESCHERICHIA COLI WITH NORMAL ENZYMATIC ACTIVITY ISOLATED FROM CHILDREN DURING THE FIRST YEAR OF LIFE.

Morphological analyses in fragility of pili torti with Björnstad syndrome.

Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome.

The primary transcriptome of the Escherichia coli O104:H4 pAA plasmid and novel insights into its virulence gene expression and regulation.

The Group A Streptococcus serotype M2 pilus plays a role in host cell adhesion and immune evasion.

Iliac Artery Aneurysms in Menkes Disease: A Case Report.

A secretome view of colonisation factors in Shiga toxin-encoding Escherichia coli (STEC): from enterohaemorrhagic E. coli (EHEC) to related enteropathotypes.

Mutation of the toxR or mshA genes from Vibrio coralliilyticus strain OCN014 reduces infection of the coral Acropora cytherea.

The Arid Melancholy-Netherton Syndrome With Protein Energy Malnutrition.

Adjuvant sunitinib or sorafenib for high-risk, non-metastatic renal-cell carcinoma (ECOG-ACRIN E2805): a double-blind, placebo-controlled, randomised, phase 3 trial.

Dermatologic findings of focal dermal hypoplasia (Goltz syndrome).

Nailfold capillaroscopic findings in primary Sjögren's syndrome with and without Raynaud's phenomenon and/or positive anti-SSA/Ro and anti-SSB/La antibodies.

Two sisters with Reed's syndrome: treatment with pregabalin.

Escherichia coli O104:H4 Pathogenesis: an Enteroaggregative E. coli/Shiga Toxin-Producing E. coli Explosive Cocktail of High Virulence.

Novel homozygous mutation, c.400C>T (p.Arg134*), in the PVRL1 gene underlies cleft lip/palate-ectodermal dysplasia syndrome in an Asian patient.

Exome sequencing reveals novel BCS1L mutations in siblings with hearing loss and hypotrichosis.

Clinical, dermoscopic, and histopathologic features of body hair disorders.

Impact of virulence genes on sepsis severity and survival in Escherichia coli bacteremia.

Global analysis of posttranscriptional regulation by GlmY and GlmZ in enterohemorrhagic Escherichia coli O157:H7.

Leiomyoma cutis: a focused review on presentation, management, and association with malignancy.