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Orphanet Journal of Rare Diseases|June 14, 2017
International physician survey on management of FOP: a modified Delphi studyMaja Di Rocco, Genevieve Baujat, Marta Bertamino, et al.
European Journal of Human Genetics : EJHG|July 24, 2019
Comprehensive clinical and molecular studies in split-hand/foot malformation: identification of two plausible candidate genes (LRP6 and UBA2)Kaori Yamoto, Hirotomo Saitsu, Gen Nishimura, et al.
Biochemical and Biophysical Research Communications|October 28, 2008
A unique mutation of ALK2, G356D, found in a patient with fibrodysplasia ossificans progressiva is a moderately activated BMP type I receptorToru Fukuda, Kazuhiro Kanomata, Junya Nojima, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|December 30, 2022
Reduction of New Heterotopic Ossification (HO) in the Open-Label, Phase 3 MOVE Trial of Palovarotene for Fibrodysplasia Ossificans Progressiva (FOP)Robert J Pignolo, Edward C Hsiao, Mona Al Mukaddam, et al.
British Journal of Clinical Pharmacology|October 4, 2018
Special considerations for clinical trials in fibrodysplasia ossificans progressiva (FOP)Edward C Hsiao, Maja Di Rocco, Amanda Cali, et al.
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