Disease: Tarsal carpal coalition syndrome
- <em>GDF6</em> Knockdown in a Family with Multiple Synostosis Syndrome and Speech Impairment
- 8 out of 10 patients do well after surgery for tarsal coalitions: A systematic review on 1284 coalitions
- A 1.6-Mb microdeletion in chromosome 17q22 leads to NOG-related symphalangism spectrum disorder without intellectual disability
- A comprehensive review of reported heritable noggin-associated syndromes and proposed clinical utility of one broadly inclusive diagnostic term: NOG-related-symphalangism spectrum disorder (NOG-SSD)
- A familial case of NOG -related symphalangism spectrum disorder due to a novel NOG variant
- A mutation in the heparin-binding site of noggin as a novel mechanism of proximal symphalangism and conductive hearing loss
- A New Subtype of Multiple Synostoses Syndrome Is Caused by a Mutation in GDF6 That Decreases Its Sensitivity to Noggin and Enhances Its Potency as a BMP Signal
- A Novel Missense Mutation of NOG Interferes With the Dimerization of NOG and Causes Proximal Symphalangism Syndrome in a Chinese Family
- A novel nonsense mutation in the NOG gene causes familial NOG-related symphalangism spectrum disorder
- A novel variant in the ROR2 gene underlying brachydactyly type B: a case report
- A point mutation in Fgf9 impedes joint interzone formation leading to multiple synostoses syndrome
- A Start Codon Variant in <em>NOG</em> Underlies Symphalangism and Ossicular Chain Malformations Affecting Both the Incus and the Stapes
- Analysis of phenotype and pathogenic variants in a Chinese pedigree affected with Multiple synostoses syndrome type 1
- Arthroscopic Calcaneonavicular Coalition and Too-long Anterior Process of the Calcaneus Resection in Children
- Arthroscopic Talocalcaneal Coalition Resection in Children
- Autopsy findings in a stillborn female infant with the Osebold-Remondini syndrome
- Autosomal dominant stapes fixation, syndactyly, and symphalangism in a family with NOG mutation: Long term follow-up on surgical treatment
- BMP antagonists in tissue development and disease
- Child calcaneonavicular coalitions: MRI diagnostic value in a 19-case series
- Clinical observation and genetic analysis of a SYNS1 family caused by novel NOG gene mutation
- Clinical value of combined single photon emission computerized tomography and conventional computer tomography (SPECT/CT) in sports medicine
- Delineation of the clinically recognizable 17q22 contiguous gene deletion syndrome in a patient carrying the smallest microdeletion known to date
- Double bilateral talocalcaneal and calcaneonavicular coalition in a 15 year-old patient: treatment and results
- Further delineation of facioaudiosymphalangism syndrome: Description of a family with a novel NOG mutation and without hearing loss
- Genetic and clinical phenotypic analysis of familial stapes sclerosis caused by an NOG mutation
- Genetic Heterogeneity and Core Clinical Features of NOG-Related-Symphalangism Spectrum Disorder
- Humeroradial synostosis and the multiple synostosis syndrome: case report
- Identical mutations in NOG can cause either tarsal/carpal coalition syndrome or proximal symphalangism
- Identification of two novel mutations in the NOG gene associated with congenital stapes ankylosis and symphalangism
- Is the Conductive Hearing Loss in NOG-Related Symphalangism Spectrum Disorder Congenital?
- Multiple synostoses syndrome: Clinical report and retrospective analysis
- Multiple synostoses syndrome: Radiological findings and orthopedic management in a single institution cohort
- Mutations in the NOG gene are commonly found in congenital stapes ankylosis with symphalangism, but not in otosclerosis
- Natural Progression and Symptomatic Management of Tarsal-Carpal Coalition Syndrome: A Case Report
- Negative mutation screening of the NOG, BMPR1B, GDF5, and FGF9 genes indicates further genetic heterogeneity of the facioaudiosymphalangism syndrome
- Novel NOG mutation in Japanese patients with stapes ankylosis with broad thumbs and toes
- P35S mutation in the NOG gene associated with Teunissen-Cremers syndrome and features of multiple NOG joint-fusion syndromes
- Proximal symphalangism and premature ovarian failure
- Seven additional families with spondylocarpotarsal synostosis syndrome with novel biallelic deleterious variants in FLNB
- Spondylocarpotarsal synostosis syndrome and cervical instability
- Spondylocarpotarsal synostosis syndrome: MRI evaluation of vertebral and disk malformation
- Standard variant venous dysplasia of the cerebellum in a patient suffering from Muenke's syndrome and tinnitus
- Stapedectomy in Teunissen-Cremers Syndrome: Intraoperative Findings and Hearing Outcomes
- Surgical Considerations for Massive Tarsal Coalitions in Multiple Synostosis Syndrome: A Case Report
- Syndrome of coronal craniosynostosis with brachydactyly and carpal/tarsal coalition due to Pro250Arg mutation in FGFR3 gene
- Syndrome of coronal craniosynostosis, Klippel-Feil anomaly, and sprengel shoulder with and without Pro250Arg mutation in the FGFR3 gene
- Talocalcaneal coalition in Muenke syndrome: report of a patient, review of the literature in FGFR-related craniosynostoses, and consideration of mechanism
- Talocalcaneal Tarsal Coalition Size: Evaluation and Reproducibility of MRI Measurements
- Tarsal and carpal coalition and symphalangism of the Fuhrmann type. Report of a family
- Tarsal tunnel syndrome in a patient on long-term peritoneal dialysis: case report
- Tarsal-carpal coalition syndrome: a familial case
- Tarsal-carpal coalition syndrome: importance of early diagnosis
- Tarsal-carpal coalition syndrome: Report of a novel missense mutation in NOG gene and phenotypic delineation
- Temporal Bone Histopathology in NOG-Symphalangism Spectrum Disorder
- The multiple synostoses syndrome. A plea for simplicity
- Variable phenotypes of multiple synostosis syndrome in patients with novel NOG mutations
- Wrist denervation in isolation: a prospective outcome study with patient selection by wrist blockade