Longitudinal patient-reported mobility assessment in fibrodysplasia ossificans progressiva (FOP)
Author:
Publisher
Elsevier BV
Subject
Histology,Physiology,Endocrinology, Diabetes and Metabolism
Reference12 articles.
1. 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
2. Fibrodysplasia ossificans progressiva: diagnosis, management, and therapeutic horizons;Pignolo;Pediatr. Endocrinol. Rev.,2013
3. A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva;Shore;Nat. Genet.,2006
4. The FOP metamorphogene encodes a novel type I receptor that dysregulates BMP signaling;Kaplan;Cytokine Growth Factor Rev.,2009
5. Cellular hypoxia promotes heterotopic ossification by amplifying BMP signaling;Wang;J. Bone Miner. Res.,2016
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2. Most Fractures Treated Nonoperatively in Individuals With Fibrodysplasia Ossificans Progressiva Heal With a Paucity of Flareups, Heterotopic Ossification, and Loss of Mobility;Clinical Orthopaedics & Related Research;2023-05-08
3. The natural history of fibrodysplasia ossificans progressiva: A prospective, global 36-month study;Genetics in Medicine;2022-12
4. The impact of fibrodysplasia ossificans progressiva (FOP) on patients and their family members: results from an international burden of illness survey;Expert Review of Pharmacoeconomics & Outcomes Research;2022-09-21
5. MyD88 Is Not Required for Muscle Injury-Induced Endochondral Heterotopic Ossification in a Mouse Model of Fibrodysplasia Ossificans Progressiva;Biomedicines;2021-06-01
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