» Articles » PMID: 3345218

Osteogenesis Imperfecta. A Model for Genetic Causes of Osteoporosis and Perhaps Several Other Common Diseases of Connective Tissue

Overview
Journal Arthritis Rheum
Specialty Rheumatology
Date 1988 Jan 1
PMID 3345218
Citations 7
Authors
Affiliations
Soon will be listed here.
Citing Articles

Collagen (I) homotrimer potentiates the osteogenesis imperfecta (oim) mutant allele and reduces survival in male mice.

Lee K, Rambault L, Bou-Gharios G, Clegg P, Akhtar R, Czanner G Dis Model Mech. 2022; 15(9).

PMID: 36106514 PMC: 9555767. DOI: 10.1242/dmm.049428.


Genetic factors in osteoporosis. What are the implications for prevention and treatment?.

Keen R, Kelly P Drugs Aging. 1997; 11(5):333-7.

PMID: 9359020 DOI: 10.2165/00002512-199711050-00001.


Reflex sympathetic dystrophy syndrome with microtrabecular fracture in a patient with osteogenesis imperfecta.

Neri R, Martini A, Trippi D, Zampa V, Pasero G Clin Rheumatol. 1997; 16(4):363-6.

PMID: 9259249 DOI: 10.1007/BF02242452.


Genetics of osteoporosis.

Brandi M, Bianchi M, Eisman J, Glorieux F, Adami S, Fiore C Calcif Tissue Int. 1994; 55(3):161-3.

PMID: 7987726 DOI: 10.1007/BF00425868.


Encephalopathy, deafness and blindness in young women: a distinct retinocochleocerebral arteriolopathy?.

Asherson R, GLEDHILL R J Neurol Neurosurg Psychiatry. 1989; 52(8):1020-1.

PMID: 2795064 PMC: 1031857. DOI: 10.1136/jnnp.52.8.1020-a.