Results 101 to 110 of about 3,792 (182)
The role of miRNAs as biomarkers in heterotopic ossification
Fibrodysplasia ossificans progressiva and progressive osseous heteroplasia are genetic forms of heterotopic ossification (HO). Fibrodysplasia ossificans progressiva is caused by ACVR1 gene mutations, while progressive osseous heteroplasia is caused by ...
Chen Xie +5 more
doaj +1 more source
Fibrodysplasia Ossificans Progressiva (FOP) [PDF]
F S, Kaplan, R M, Smith
openaire +2 more sources
Fibrodysplasia ossificans progressiva is a rare autosomal dominantly inherited disorder of connective tissue caused by mutations in the gene encoding for ACVR1/ALK2, a bone morphogenetic protein type I receptor.
Mohammed Saleh +4 more
doaj +1 more source
A new spontaneous model of fibrodysplasia ossificans progressiva. [PDF]
Fibrodisplasia ossificante progressiva (FOP) é uma doença genética caracterizada por uma acentuada, progressiva e aparentemente incontrolável ossificação dos tendões, ligamentos, faciais e músculos estriados da formação de osso heterotópico resultando na
Martin, Larry D. +2 more
core
The Fibrodysplasia Ossificans Progressiva and Bone Scintigraphy
Fibrodysplasia ossificans progressiva (FOP) is an exceptionally rare autosomal dominant condition characterized by malformations of the big toes and progressive extra-skeletal ossifications in distinct anatomical patterns.
Sofia CHKIKAR +2 more
doaj +1 more source
Caring for Individuals with Fibrodysplasia Ossificans Progressiva (FOP): A Treatment Manual for Occupational Therapists [PDF]
Fibrodysplasia Ossificans Progressiva is a rare and disabling genetic disorder that results in ossification of the soft tissues (Kaplan, Xu, et al., 2008; Kocyigit, Hizil, Hemis, Sabah, & Memis, 2001).
Rositas, Amanda, Zavoral, Kathryn
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Fibrodysplasia Ossificans Progressiva
Aniket N, Tavare, Jane, Young
openaire +3 more sources
Case Report of Fibrodysplasia Ossificans Progressiva [PDF]
Fibrodysplasia ossificans progressiva is a rare genetic disease characterized by widespread soft tissue ossification and congenital stigmata of the extremities. We report a male patient who had bilateral hallux valgus since birth. Other noticed anomalies
M, Vishwanath +5 more
core +1 more source

