Clinical staging of Fibrodysplasia Ossificans Progressiva (FOP)-Reference-Cited by-同舟云学术

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Clinical staging of Fibrodysplasia Ossificans Progressiva (FOP)

Published:2018-04 Issue: Volume:109 Page:111-114
ISSN:8756-3282
Container-title:Bone
language:en
Short-container-title:Bone

Author:

Pignolo Robert J.,Kaplan Frederick S.

Funder

Mayo Clinic

Radiant Hope Foundation

International Fibrodysplasia Ossificans Progressiva Association

University of Pennsylvania Perelman School of Medicine

Ian Cali Endowment

Whitney Weldon Endowment

Isaac and Rose Nassau Professorship of Orthopaedic Molecular Medicine

Publisher

Elsevier BV

Subject

Histology,Physiology,Endocrinology, Diabetes and Metabolism

Reference10 articles.

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

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

5. A cumulative analogue joint involvement scale (CAJIS) for fibrodysplasia ossificans progressiva (FOP);Kaplan;Bone,2017

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4. Patient-nurse ratio as an index related to healthcare-associated infections: a surveillance study;Boletín Médico del Hospital Infantil de México;2023-03-03

5. Garetosmab, an inhibitor of activin A, reduces heterotopic ossification and flare-ups in adults with fibrodysplasia ossificans progressiva: a randomized, double-blind, placebo-controlled phase 2 trial;2023-01-12

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