Osteogenesis imperfecta

LE WE PMID CA

Osteogenesis imperfecta

2062

Osteogenesis imperfecta

ERS UFR (Induced Mediators)

Fibrous dysplasia

FKBP65

LEPRE1

Osteogenesis imperfecta

Protein (Transport Retrotransport ER to CP)

2009 1	Effects of bisphosphonates in children with osteogenesis imperfecta: an AACPDM systematic review. [19087101] Dev Med Child Neurol 51(1): 17-29 (2009)
1990 2	Morphological changes in growth-plate cartilage in osteogenesis imperfecta. [2187879] J Bone Joint Surg Br 72(3): 475-9 (1990)
1995 3	Osteogenesis imperfecta, non-accidental injury, and temporary brittle bone disease. [7702388] Arch Dis Child 72(2): 169-71; discussion 171-6 (1995)
2003 4	Improvement of bone in patients with osteogenesis imperfecta treated with pamidronate-lessons from biochemistry. [12629072] J Clin Endocrinol Metab 88(3): 984-5 (2003)
1991 5	Osteogenesis imperfecta: translation of mutation to phenotype. [1895312] J Med Genet 28(7): 433-42 (1991)
2003 6	Abnormalities in the cerebral arterial system in osteogenesis imperfecta. [12695216] AJNR Am J Neuroradiol 24(4): 748-50 (2003)
2002 7	Mutations in type I collagen genes resulting in osteogenesis imperfecta in humans. [12362985] Acta Biochim Pol 49(2): 433-41 (2002)
2011 8	Endoplasmic reticulum stress or mutation of an EF-hand Ca(2+)-binding domain directs the FKBP65 rotamase to an ERAD-based proteolysis. [21761186] Cell Stress Chaperones 16(6): 607-19 (2011)
2010 9	Current and emerging treatments for the management of osteogenesis imperfecta. [20856683] Ther Clin Risk Manag 6(-): 367-81 (2010)
2011 10	Bisphosphonates' : Indications in bone diseases other than osteoporosis. [21681711] Tunis Med 89(6): 511-6 (2011)
2010 11	Null mutations in LEPRE1 and CRTAP cause severe recessive osteogenesis imperfecta. [19862557] Cell Tissue Res 339(1): 59-70 (2010)

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