Author:
Towler O. Will,Shore Eileen M.,Kaplan Frederick S.
Funder
nternational Fibrodysplasia Ossificans Progressiva Association
enter for Research in FOP and Related Disorders
an Cali Endowment for FOP Research
hitney Weldon Endowment for FOP Research
saac & Rose Nassau Professorship of Orthopaedic Molecular Medicine
ali-Weldon Professorship of FOP Research
Subject
Histology,Physiology,Endocrinology, Diabetes and Metabolism
Reference42 articles.
1. Inherited human diseases of heterotopic bone formation;Shore;Nat. Rev. Rheumatol.,2010
2. Genetic disorders of heterotopic ossification: Fibrodysplasia ossificans progressiva and progressive osseous heteroplasia (chapter 112, pp. 865–870);Kaplan,2019
3. Age- and joint-specific risk of initial heterotopic ossification in patients who have fibrodysplasia ossificans progressiva;Rocke;Clin. Orthop. Relat. Res.,1994
4. The natural history of flare-ups in fibrodysplasia ossificans progressiva (FOP): a comprehensive global assessment;Pignolo;J. Bone Miner. Res.,2016
5. A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva;Shore;Nat. Genet.,2006
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