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Výsledek výzkumu

Effect of alendronate therapy in children with osteogenesis imperfecta

Effect of alendronate therapy in children with osteogenesis imperfecta.

FP - Ostatní lékařské obory

  • 2005
  • Jx
Výsledek výzkumu

Quantitative ultrasonometry of the calcaneus in children with osteogenesis imperfecta

Ultrasound parameters of calcaneal bone quality are low in children with osteogenesis imperfecta andare not related to number of prevalent fractures....

FG - Pediatrie

  • 2010
  • Jx
Výsledek výzkumu

Osteogenesis imperfecta.

Osteogenesis imperfecta is an inheritable connective tissue disorder with variable phenotypic expression. Quantitative and qualitative of the genetic error in type I collagen foramation are typical in the 90 % of pateints....

FI - Traumatologie a ortopedie

  • 2010
  • Jx
Výsledek výzkumu

Osteogenesis imperfecta in childhood on the part of clinician

State of art information about different types, hereditability, and treatment possibilities of osteogenesis imperfecta, main cause of genetically determined status of brittle bones in children....

FG - Pediatrie

  • 2011
  • Jx
Výsledek výzkumu

Osteogenesis imperfecta in children - what attending physicians should know

Treatment of osteogenesis imperfecta requires careful cooperation of physician and family since birth of the child. This review should be source of information for all attending physicians....

FG - Pediatrie

  • 2009
  • Jx
Výsledek výzkumu

Collagen type I gene mutations of alpha 1 chain (Col1A1) in Czech patients with Osteogenesis Imperfecta Syndrome

Collagen gene mutations in patients with osteogenesis imperfecta syndrome. Comparison of genotype and phenotype.

EB - Genetika a molekulární biologie

  • 2003
  • Jx
Výsledek výzkumu

Etiology of Osteogenesis Imperfecta: COL1A1 Gene Mutations in Czech Patients

Osteogenesis imperfecta (OI) is caused by collagen gene mutations. Authors describe a group of patients with OI from clinical and genetical aspects - with the interest of phenotype and genotype comparison....

EB - Genetika a molekulární biologie

  • 2003
  • D
Výsledek výzkumu

COL1A2 gene analysis in a Czech osteogenesis imperfecta patient: a candidate novel mutation in a patient affected by osteogenesis imperfecta type 3

Osteogenesis imperfecta is a heritable bone fragility disease and radiographic features as having type 3 osteogenesis imperfecta, which is a severe form provides both evidence of a novel COL1A2 mutation resulting i...

EB - Genetika a molekulární biologie

  • 2015
  • Jx
  • Odkaz
Výsledek výzkumu

Osteogenesis imperfecta, type IA

The authors present a case report of osteogenesis imperfecta, type I. There are described characteristic clinical features and molecular-genetic origin of the disease. Case report is accompanied by visual documentation and results o...

FG - Pediatrie

  • 2016
  • Jx
  • Odkaz
Výsledek výzkumu

Etiology of Osteogenesis Imperfecta: COL1A1 Gene Mutations in Czech Patients

Etiology, different type of mutations, col 1 A 1 gene...

EB - Genetika a molekulární biologie

  • 2003
  • C
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