Results 101 to 110 of about 3,838 (202)

A 24-year-old man with fibrodysplasia ossificans progressiva: clinical challenges and management [PDF]

Fibrodysplasia ossificans progressiva (FOP) is a rare, disabling genetic disorder characterized by progressive heterotopic ossification of skeletal muscles and connective tissues.
Abdal, Syed Jamil, Haq, Syed Atiqul, Islam, M. Ariful, Nahar, Sharmin, Shahin, M. Abu, Yesmin, Sabrina   +5 more
core   +2 more sources

Heterotope Ossifikation: Von der Ätiologie zur aktuellen Therapie [PDF]

, 2018
Zusammenfassung: Heterotope Ossifikationen werden als abnorme Bildung von Knochen in Weichteilgeweben definiert. Man unterscheidet die erworbene von den angeborenen Formen.
Bauer, S., Cadosch, D., Filgueira, L., Gautschi, O.P., Zellweger, R.   +4 more
core  

Fibrodysplasia Ossificans Progressiva (FOP) [PDF]

Journal of Bone and Mineral Research, 1997
F S, Kaplan, R M, Smith
openaire   +2 more sources

Anaesthetic considerations in a child with fibrodysplasia ossificans progressiva [PDF]

, 2019
Fibrodysplasia ossificans progressiva (FOP) is an extremely rare genetic disorder characterised by extraskeletal ossification of connective tissue. Affected individuals often become completely immobilised by their third decade of life.
Kleyenstüber, Thomas
core   +1 more source

The role of miRNAs as biomarkers in heterotopic ossification

EFORT Open Reviews
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, Xiao Liu, Wenbao Li, Zhaozhe Yao, Hongyue Men, Zongyu Li   +5 more
doaj   +1 more source

Fibrodysplasia ossificans progressiva

Rheumatology, 2019
Uma Kumar, Shiv Kumar Suman, Sauvik Dasgupta, Rajiv Ranjan Kumar   +3 more
openaire   +2 more sources

The Fibrodysplasia Ossificans Progressiva and Bone Scintigraphy

Swiss Journal of Radiology and Nuclear Medicine
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, Assia SEDDOUKI, Nadia ISMAILI ALAOUI   +2 more
doaj   +1 more source

Fibrodysplasia Ossificans Progressiva

JCR: Journal of Clinical Rheumatology, 2015
Aniket N, Tavare, Jane, Young
openaire   +3 more sources

Issue Information

Rheumatology &Autoimmunity, Volume 5, Issue 1, Page 1-4, March 2025.
wiley   +1 more source

Quality of life of patients with fibrodysplasia ossificans progressiva [PDF]

, 2015

core   +1 more source