Found: 12
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Relationship Among VDR (BsmI and FokI), COLIA1, and CTR Polymorphisms with Bone Mass, Bone Turnover Markers, and Sex Hormones in Men.
- Published in:
- Calcified Tissue International, 2002, v. 70, n. 6, p. 457, doi. 10.1007/s00223-001-1088-9
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- Publication type:
- Article
Association of CTR and COLIA1 alleles with BMD values in peri- and postmenopausal women.
- Published in:
- 2000
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- Publication type:
- journal article
Deficiency of CRTAP in non-lethal recessive osteogenesis imperfecta reduces collagen deposition into matrix.
- Published in:
- Clinical Genetics, 2012, v. 82, n. 5, p. 453, doi. 10.1111/j.1399-0004.2011.01794.x
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- Publication type:
- Article
Osteogenesis imperfecta: clinical, biochemical and molecular findings.
- Published in:
- Clinical Genetics, 2006, v. 70, n. 2, p. 131, doi. 10.1111/j.1399-0004.2006.00646.x
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- Publication type:
- Article
THE NEED FOR FEDERAL PREEMPTION OF STATE TORT CLAIMS IN THE CONTEXT OF "NEW DRUGS" AND PREMARKET-APPROVED MEDICAL DEVICES.
- Published in:
- 2011
- By:
- Publication type:
- Opinion
Association of BK virus with human brain tumors and tumors of pancreatic islets.
- Published in:
- International Journal of Cancer, 1987, v. 39, n. 1, p. 60, doi. 10.1002/ijc.2910390111
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- Publication type:
- Article
Osteoporosis in β-Thalassemia: Clinical and Genetic Aspects.
- Published in:
- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 451, doi. 10.1196/annals.1345.051
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- Publication type:
- Article
Bone histomorphometry in acromegaly patients with fragility vertebral fractures.
- Published in:
- Pituitary, 2018, v. 21, n. 1, p. 56, doi. 10.1007/s11102-017-0847-1
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- Publication type:
- Article
Increased Gene Expression of RUNX2 and SOX9 in Mesenchymal Circulating Progenitors Is Associated with Autophagy during Physical Activity.
- Published in:
- Oxidative Medicine & Cellular Longevity, 2019, p. 1, doi. 10.1155/2019/8426259
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- Publication type:
- Article
Detection of mutations in the ALD gene (ABCD1) in seven Italian families: Description of four novel mutations.
- Published in:
- Human Mutation, 2000, v. 16, n. 3, p. 271, doi. 10.1002/1098-1004(200009)16:3<271::AID-HUMU15>3.0.CO;2-D
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- Publication type:
- Article
Severe (type III) osteogenesis imperfecta due to glycine substitutions in the central domain of the collagen triple helix.
- Published in:
- Human Molecular Genetics, 1994, v. 3, n. 12, p. 2201
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- Publication type:
- Article
Osteogenesis Imperfecta: Practical Treatment Guidelines.
- Published in:
- Pediatric Drugs, 2000, v. 2, n. 6, p. 465, doi. 10.2165/00128072-200002060-00005
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- Publication type:
- Article