Clinical-pathological correlations in three patients with fibrodysplasia ossificans progressiva-Reference-Cited by-同舟云学术

Clinical-pathological correlations in three patients with fibrodysplasia ossificans progressiva

Published:2018-04 Issue: Volume:109 Page:104-110
ISSN:8756-3282
Container-title:Bone
language:en
Short-container-title:Bone

Author:

Wentworth Kelly L.,Bigay Katherine,Chan Tea V.,Ho Jennifer P.,Morales Blanca M.,Connor Joseph,Brooks Erin,Shahriar Salamat M.,Sanchez Henry Charles,Wool Geoffrey,Pignolo Robert J.,Kaplan Frederick S.,Hsiao Edward C.

Funder

UCSF/Eli and Edythe Broad Fellowship

Wilsey Family Fellowship

Doris Duke Charitable Fund

March of Dimes

Radiant Hope Foundation

Mayo Clinic

Clementia Pharmaceuticals for FOP Clinical Research Studies

Publisher

Elsevier BV

Subject

Histology,Physiology,Endocrinology, Diabetes and Metabolism

Reference22 articles.

1. The natural history of flare-ups in Fibrodysplasia Ossificans Progressiva (FOP): a comprehensive global assessment;Pignolo;J. Bone Miner. Res.,2016

2. Age- and joint-specific risk of initial heterotopic ossification in patients who have fibrodysplasia ossificans progressiva;Rocke;Clin. Orthop. Relat. Res.,1994

3. 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

4. Fibrodysplasia ossificans progressiva: clinical and genetic aspects;Pignolo;Orphanet J. Rare Dis.,2011

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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