Literature DB >> 5033743

Polyostotic fibrous dysplasia and myositis ossificans progressiva. A report of coexistence.

B Frame, N Azad, W A Reynolds, S M Saeed.   

Abstract

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Mesh：

Year:  1972        PMID： 5033743     DOI： 10.1001/archpedi.1972.02110130122020

Source DB:  PubMed          Journal:  Am J Dis Child        ISSN： 0002-922X


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  3 in total

Review 1.  Sleep in Parkinson's disease.

Authors:  Ambra Stefani; Birgit Högl
Journal:  Neuropsychopharmacology       Date:  2019-06-24       Impact factor: 7.853

2.  Classic and atypical fibrodysplasia ossificans progressiva (FOP) phenotypes are caused by mutations in the bone morphogenetic protein (BMP) type I receptor ACVR1.

Authors:  Frederick S Kaplan; Meiqi Xu; Petra Seemann; J Michael Connor; David L Glaser; Liam Carroll; Patricia Delai; Elisabeth Fastnacht-Urban; Stephen J Forman; Gabriele Gillessen-Kaesbach; Julie Hoover-Fong; Bernhard Köster; Richard M Pauli; William Reardon; Syed-Adeel Zaidi; Michael Zasloff; Rolf Morhart; Stefan Mundlos; Jay Groppe; Eileen M Shore
Journal:  Hum Mutat       Date:  2009-03       Impact factor: 4.878

3.  Fibrodysplasia ossificans progressiva and synovial chondromatosis.

Authors:  G Kalifa; C Adamsbaum; C Job-Deslande; J Dubousset
Journal:  Pediatr Radiol       Date:  1993
  3 in total

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