Results 151 to 160 of about 2,707 (209)

Giant ischial osteochondroma causing ischiofemoral impingement and sciatic nerve compression in a pediatric patient with Albright's hereditary osteodystrophy. [PDF]

Radiol Case Rep
Jebackumar T, Johnson R, Schroeder A, Silveri C, Lesensky J, Belzarena AC.   +5 more
europepmc   +1 more source

Bessel-Hagen Disease: A Case Report of a Rare Disease. [PDF]

Cureus
Ammor F, Gourti M, Lefqih I, Maidi E.
europepmc   +1 more source

Osteochondroma

, 2019
openaire   +1 more source

Fibrodysplasia ossificans progressiva in children: diagnostic pitfalls and ACVR1 genotype-phenotype spectrum. [PDF]

Eur J Pediatr
Acikgoz NB, Senkalfa B, Celik Ertas B, Ozdemir Uslu Z, Helhel E, Urel Demir G, Alanay Y, Yildiz AE, Utine GE, Ozon ZA, Simsek Kiper PO.   +10 more
europepmc   +1 more source

Intermetatarsal osteochondroma in a pediatric patient: a rare case of chronic foot pain and surgical resolution. [PDF]

J Surg Case Rep
Alhuzaimi F, Alabdulkarim N, Alanezi M, Alshayhan F, Alrajhi AM.   +4 more
europepmc   +1 more source

Osteochondroma

, 2013
openaire   +1 more source

Osteochondroma

, 2010
openaire   +1 more source

The Rizzoli Multiple Osteochondromas Classification revised: describing the phenotype to improve clinical practice [PDF]

American Journal of Medical Genetics, Part A, 2021
Multiple osteochondromas (MO) is a rare disorder, characterized by benign osteocartilaginous tumors (osteochondromas), arising from the perichondrium of bones.
Marina Mordenti, Maria Gnoli, Manila Boarini   +2 more
exaly   +2 more sources

Multiple osteochondromas in the archaeological record: a global review

Journal of Archaeological Science, 2010
Multiple osteochondromas is an inherited autosomal dominant condition of enchondral bone growth. The paper undertakes the first synthesis study of the 16 known cases of the condition that have been identified in the international palaeopathological ...
Eileen M Murphy
exaly   +2 more sources