Chemical and biomechanical characterization of hyperhomocysteinemic bone disease in an animal model

Author:

Massé Priscilla G,Boskey Adele L,Ziv Israel,Hauschka Peter,Donovan Sharon M,Howell David S,Cole David EC

Publisher

Springer Science and Business Media LLC

Subject

Orthopedics and Sports Medicine,Rheumatology

Reference61 articles.

1. Mudd SH, Levy HL, Kraus JP: Disorders of transsulfuration. In: The metabolic and molecular bases of inherited disease. Edited by: Scriver CR, Beaudet AL, Sly WS, Valle D. 2001, New York: McGraw Hill Inc., 2007-2056.

2. Schedewie H, Willich E, Grobe H, Schmidt H, Muller KM: Skeletal findings in homocystinuria: A collaborative study. Pediat Radiol. 1973, 1: 12-23.

3. Brenton DP: Skeletal abnormalities in homocystinuria. Postgrad Med J. 1977, 53: 488-494.

4. Mudd SH, Skovby F, Levy HL, Pettigrew KD, Wilcken B, Pyeritz RE, et al: The natural history of homocystinuria due to cystathionine β-synthase deficiency. Am J Hum Genet. 1985, 37: 1-31.

5. Parrot F, Redonnet-Vernhet I, Lacombe D, Gin H: Osteoporosis in late-diagnosed adult homocystinuric patients. J Inherit Metab Dis. 2000, 23: 338-340. 10.1023/A:1005618927729.

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