Hajdu-Cheney Syndrome With Coexisting Rheumatoid Arthritis: A Diagnostic Challenge.

Unexpected genotypes associated with severe paediatric conditions identified in a healthy population cohort.

Bathrocephaly and Serpentine Fibula as Underrated Features of Osteogenesis Imperfecta Type I: A Case Report.

Temporal Bone CT Findings in Hajdu-Cheney Syndrome: Case Report with Review of the Literature.

Temporal Bone Osseous Dysplasia With Conductive Hearing Loss in Hajdu-Cheney Syndrome.

Hajdu-Cheney Syndrome with Fatal Progressive Basilar Invagination: Illustrative Case.

Periodontal Manifestations of Systemic Diseases.

Bone mineral density and microarchitecture improvement in a young patient with Hajdu-Cheney syndrome and autosomal dominant polycystic kidney disease treated with alendronate.

Notch2 Signaling Drives Cardiac Hypertrophy by Suppressing Purine Nucleotide Metabolism.

Hajdu-Cheney Syndrome, a Rare Cause of Acro-Osteolysis and Osteoporosis With Zoledronic Acid Experience.

Notch2 Inhibition and Kidney Cyst Growth in Autosomal Dominant Polycystic Kidney Disease.

A NOTCH2 pathogenic variant and HES1 regulate osteoclastogenesis in induced pluripotent stem cells.

Hajdu-Cheney syndrome: A case of acral osteolytic deformity of both hands.

Anaesthesia for a patient of Hajdu Cheney syndrome scheduled for scoliosis surgery-A case study.

First case of Hajdu-Cheney syndrome in Lithuania caused by novel NOTCH2 gene likely pathogenic variant.

Japanese siblings with multicentric osteolysis nodulosis and arthropathy.

NOTCH2 promotes osteoclast maturation and metabolism and modulates the transcriptome profile during osteoclastogenesis.

Multicentric Carpo-Tarsal Osteolysis Syndrome (MCTO) and "Function Profile": a rehabilitative approach.

Cranial vault suspension for basilar invagination in patients with open cranial sutures: technique and long-term follow-up. Illustrative case.

Solitary Band Acro-osteolysis in Hajdu-Cheney Syndrome.

NOTCH2 sensitizes the chondrocyte to the inflammatory response of tumor necrosis factor α.

Acroosteolysis and facial dysmorphia: a new case of Hajdu-Cheney syndrome.

Clinical, radiographic and molecular characterization of two unrelated families with multicentric osteolysis, nodulosis, and arthropathy.

Hajdu-Cheney syndrome with a novel variant in NOTCH2 gene: A case report.

Fracture healing in a mouse model of Hajdu-Cheney-Syndrome with high turnover osteopenia results in decreased biomechanical stability.

A case of safe airway management by fiber-optic nasotracheal intubation in general anesthesia in a pediatric patient with Hajdu-Cheney syndrome: a case report.

Orofacial characteristics in a child with Hajdu-Cheney syndrome.

NOTCH2 related disorders: Description and review of the fetal presentation.

Exploratory use of romosozumab for osteoporosis in a patient with Hajdu-Cheney syndrome: a case report.

[A case of Hajdu-Cheney syndrome].

Hajdu-Cheney syndrome with atypical cardiovascular abnormalities.

Scoliosis Correction in an Adolescent With Hajdu-Cheney Syndrome: A Case Report.

Progress and Current Status in Hajdu-Cheney Syndrome with Focus on Novel Genetic Research.

Surgical management of high-grade lumbar spondylolisthesis associated with Hajdu-Cheney syndrome: illustrative case.

Hajdu-Cheney Syndrome: A Novel NOTCH2 Mutation in a Spanish Child in Treatment with Vibrotherapy: A Case Report.

Nursing Care Plan for Patients with Hajdu-Cheney Syndrome.

Premature Loss of Deciduous Teeth as a Symptom of Systemic Disease: A Narrative Literature Review.

Hajdu-Cheney Syndrome: Report of a Case in Spain.

Novel phenotypic feature in a patient with a recurrent NOTCH2 nonsense mutation.

Craniospinal Surgery in Hajdu-Cheney Syndrome: A Review of Case Reports.

Hajdu Cheney syndrome; A novel NOTCH2 mutation in a Syrian child, and treatment with zolidronic acid: A case report and a literature review of treatments.

Hairy and enhancer of split 1 is a primary effector of NOTCH2 signaling and induces osteoclast differentiation and function.

Operative Management of Spinal Deformity Secondary to Hajdu-Cheney Syndrome.

Oral Surgery Procedures in a Patient with Hajdu-Cheney Syndrome Treated with Denosumab-A Rare Case Report.

Clinical relevance of targeted exome sequencing in patients with rare syndromic short stature.

Hajdu-Cheney Syndrome: A Report on Successful Halting of Acro-osteolysis.

A family with partially penetrant multicentric carpotarsal osteolysis due to gonadal mosaicism: First reported case.

Hajdu‑Cheney syndrome: the first case report in Poland?

Skeletal characterization in a patient with Hajdu-Cheney syndrome undergoing total knee arthroplasty.

Hajdu Cheney Syndrome due to NOTCH2 defect - First case report from Pakistan and review of literature.

Hajdu-Cheney Syndrome: A Systematic Review of the Literature.

Obstructive hydrocephalus treated with endoscopic third ventriculostomy in a patient with Hajdu-Cheney syndrome: case report.

A mutation in NOTCH2 gene first associated with Hajdu-Cheney syndrome in a Greek family: diversity in phenotype and response to treatment.

Notch signaling regulates Akap12 expression and primary cilia length during renal tubule morphogenesis.

Hand Deformities in Hajdu-Cheney Syndrome: A Case Series of 3 Patients Across 3 Consecutive Generations.

Distinct severity of phenotype in Hajdu-Cheney syndrome: a case report and literature review.

Antisense oligonucleotides targeting Notch2 ameliorate the osteopenic phenotype in a mouse model of Hajdu-Cheney syndrome.

Off-label uses of denosumab in metabolic bone diseases.

The Hajdu Cheney mutation sensitizes mice to the osteolytic actions of tumor necrosis factor α.

A novel mutation in the matrix metallopeptidase 2 coding gene associated with intrafamilial variability of multicentric osteolysis, nodulosis, and arthropathy.

Multicentric osteolytic syndromes represent a phenotypic spectrum defined by defective collagen remodeling.

Phenotypic presentations of Hajdu-Cheney syndrome according to age - 5 distinct clinical presentations.

The Age Dependent Progression of Hajdu-Cheney Syndrome in Two Families.

Fatal case of Hajdu-Cheney syndrome with idiopathic pulmonary hemosiderosis.

Congenital Glaucoma: a Novel Ocular Manifestation of Hajdu-Cheney Syndrome.

A 23-year follow-up of a male with Hajdu-Cheney syndrome due to NOTCH2 mutation.

Notch signaling suppresses glucose metabolism in mesenchymal progenitors to restrict osteoblast differentiation.

A Notch in the joint that exacerbates osteoarthritis.

Mice harboring a Hajdu Cheney Syndrome mutation are sensitized to osteoarthritis.

Phenotype variability in Hajdu-Cheney syndrome.

Bisphosphonate therapy for spinal osteoporosis in Hajdu-Cheney syndrome - new data and literature review.

Dental implications in Hajdu-Cheney syndrome: A novel case report and review of the literature.

An unusual presentation of intracranial meningioma in Hajdu-Cheney syndrome.

Induction of the Hajdu-Cheney Syndrome Mutation in CD19 B Cells in Mice Alters B-Cell Allocation but Not Skeletal Homeostasis.

Osseous sarcoidosis with lupus pernio.

Foot Deformities in Hajdu-Cheney Syndrome: A Rare Case Report and Review of the Literature.

A Novel Mutation of Notch homolog protein 2 gene in a Chinese Family with Hajdu-Cheney Syndrome.

NOTCH2 Hajdu-Cheney Mutations Escape SCFFBW7-Dependent Proteolysis to Promote Osteoporosis.

Extreme proximal junctional kyphosis-a complication of delayed lambdoid suture closure in Hajdu-Cheney syndrome: a case report and literature review.

The Hajdu Cheney Mutation Is a Determinant of B-Cell Allocation of the Splenic Marginal Zone.

Clinical and experimental aspects of notch receptor signaling: Hajdu-Cheney syndrome and related disorders.

Bone Structural Characteristics and Response to Bisphosphonate Treatment in Children With Hajdu-Cheney Syndrome.

High Bone Turnover in Mice Carrying a Pathogenic Notch2 Mutation Causing Hajdu-Cheney Syndrome.

A case of Hajdu-Cheney syndrome associated with psoriatic rheumatism, two causes of acro-osteolysis.

Sustained Notch2 signaling in osteoblasts, but not in osteoclasts, is linked to osteopenia in a mouse model of Hajdu-Cheney syndrome.

The developmental biology of genetic Notch disorders.

An Antibody to Notch2 Reverses the Osteopenic Phenotype of Hajdu-Cheney Mutant Male Mice.

MAFB Determines Human Macrophage Anti-Inflammatory Polarization: Relevance for the Pathogenic Mechanisms Operating in Multicentric Carpotarsal Osteolysis.

NOTCH2 genetic mutation and acro-osteolysis-the Hajdu-Cheney syndrome.

Osseointegration of Dental Implants in a Patient with Hajdu-cheney Syndrome.

Poster 315 Complications Associated with Hajdu-Cheney Syndrome: A Case Report.

Hajdu Cheney Syndrome; report of a novel NOTCH2 mutation and treatment with denosumab.

Hajdu-Cheney syndrome - a rare cause of micrognathia.

End-Stage Renal Disease in an Infant With Hajdu-Cheney Syndrome.

Hajdu-Cheney Syndrome, a Disease Associated with NOTCH2 Mutations.

Osteoblast-specific Notch2 inactivation causes increased trabecular bone mass at specific sites of the appendicular skeleton.

Images in Medicine - Hajdu-Cheney Syndrome: A Rare Case Report.

Hajdu Cheney Mouse Mutants Exhibit Osteopenia, Increased Osteoclastogenesis, and Bone Resorption.

Capillaroscopic findings in a case of Hajdu-Cheney syndrome.

Expert's comment concerning Grand Rounds case entitled "Surgical challenges in the management of cervical kyphotic deformity in patients with severe osteoporosis: an illustrative case of a patient with Hajdu-Cheney syndrome" (T. A. Mattei, A. A. Rehman, A. Issawi, D. R. Fassett).

Surgical challenges in the management of cervical kyphotic deformity in patients with severe osteoporosis: an illustrative case of a patient with Hajdu-Cheney syndrome.

A very rare cause of acro-osteolysis: Hajdu-Cheney syndrome.

[Bilateral Instability of the Interphalangeal Articulation of the Thumb in Hajdu-Cheney Syndrome].

Primary osteolysis syndromes: beware of difficult airway.

A novel NOTCH2 mutation identified in a Korean family with Hajdu-Cheney syndrome showing phenotypic diversity.