Fibrodysplasia ossificans progressiva in China
Author:
Funder
National Natural Science Foundation of China
Publisher
Elsevier BV
Subject
Histology,Physiology,Endocrinology, Diabetes and Metabolism
Reference12 articles.
1. A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva;Shore;Nat. Genet.,2006
2. Classic and atypical fibrodysplasia ossificans progressiva (FOP) phenotypes are caused by mutations in the bone morphogenetic protein (BMP) type I receptor ACVR1;Kaplan;Hum. Mutat.,2009
3. A recurrent mutation c.617G>A in the ACVR1 gene causes fibrodysplasia ossificans progressiva in two Chinese patients;Sun;Calcif. Tissue Int.,2009
4. Iatrogenic harm caused by diagnostic errors in fibrodysplasia ossificans progressiva;Kitterman;Pediatrics,2005
5. The phenotype and genotype of fibrodysplasia ossificans progressiva in China: a report of 72 cases;Zhang;Bone,2013
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1. The serum levels of activin A and bone morphogenetic protein-4 and -6 in patients with fibrodysplasia ossificans progressiva;Orphanet Journal of Rare Diseases;2023-05-10
2. Fibrodysplasia ossificans progressiva in Hong Kong—A case report series;Frontiers in Pediatrics;2023-04-25
3. New insights on fibrodysplasia ossificans progressiva: discussion of an autoptic case report and brief literature review;Intractable & Rare Diseases Research;2021
4. Metformin attenuates trauma‐induced heterotopic ossification via inhibition of Bone Morphogenetic Protein signalling;Journal of Cellular and Molecular Medicine;2020-11-10
5. Serum osteocalcin level is associated with the mortality in Chinese patients with Fibrodysplasia ossificans progressiva aged ≤18 years at diagnosis;BMC Musculoskeletal Disorders;2020-07-31
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