Results 121 to 130 of about 17,499 (218)

Osteogenesis Imperfecta Type II (Two Autopsy Cases)

, 1982
Osteogenesis imperfecta is one of common hereditary anomalies, but its spectrum appears quite broad. There are many clinical and pathological features which suggest heterogeneity of this disease.
이병두, 지제근, 김우호
core  

Protrusio Acetabuli in Osteogenesis Imperfecta: A Two-Center Study on Incidence and Associated Factors. [PDF]

Calcif Tissue Int
Gjættermann M, Laufer A, Hald JD, Rölfing JD, Vogt B, Møller-Madsen B.   +5 more
europepmc   +1 more source

Osteogenesis imperfecta type V : spot diagnosis

, 2010
Background: The first case of Osteogenesis Imperfecta Type V in the Polish literature is reported. Case Report: Skeletal survey of an 8 year old girl with a history of multiple fractures and bilateral dislocation of radial heads was received for ...
Kozlowski, Kazimierz
core  

Severe Aortic Regurgitation in Osteogenesis Imperfecta Complicated by Mediastinal Hematoma. [PDF]

JACC Case Rep
Yamamoto A, Kitagawa T, Hirao Y, Haraguchi T, Ohashi Y.   +4 more
europepmc   +1 more source

Progressive Conductive Hearing Loss in Osteogenesis Imperfecta (Lobstein Disease): A Case Report. [PDF]

J Otol
Messaoudi K, Ait Mesbah N, Yahi N.
europepmc   +1 more source

Correction: Eruptive Process in Children with Osteogenesis Imperfecta. [PDF]

Calcif Tissue Int
Garcete Delvalle CS, De Nova García MJ, Mourelle Martínez MR.   +2 more
europepmc   +1 more source

Surgical Treatment of Tibial Tubercle Fractures in Osteogenesis Imperfecta: A Restrospective Case Series. [PDF]

J Pediatr Soc North Am
Dure A, Niu EL, Sheppard E, Martin BD, Tosi LL, Ahmed SI.   +5 more
europepmc   +1 more source

Can Telemedicine Support the Management of Osteogenesis Imperfecta? [PDF]

Acta Ortop Bras
Costa PHMMV, Nakamuta FHV, Nishida VYA, Goiano EO, Akkari M, Santili C.   +5 more
europepmc   +1 more source

Osteogenesis Imperfecta: Case Report and Literature Review

Osteogenesis imperfecta or brittle bone disease is a disorder of congenital bone fragility caused by genetic mutations in the procollagen type 1 code (COL1A1 and COL1A2). The global prevalence of children born with osteogenesis imperfecta is estimated to
Purnaning, Dyah, Mahendra, I Gede Bramantya Surya   +1 more
core  

Management of Osteogenesis Imperfecta Complicated by Severe Pneumonia in a Resource-Limited Setting: A Case Report. [PDF]

Case Rep Pediatr
Shah BK, Koirala D, Upreti S, Mahato M, Mishra B, Sapkota R, Chaudhary DR.   +6 more
europepmc   +1 more source