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Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
January 5, 2002
Preonset studies of spondyloepiphyseal dysplasia tarda caused by a novel 2-base pair deletion in SEDL encoding sedlin
S Mumm, X Zhang, G S Gottesman, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
October 1, 1996
Creatine kinase brain isoenzyme (BB-CK) presence in serum distinguishes osteopetroses among the sclerosing bone disorders
M P Whyte, A Chines, D P Silva, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 14, 1997
Extraskeletal osteoclastomas responsive to dexamethasone treatment in Paget bone disease
K Ziambaras, W A Totty, S L Teitelbaum, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
May 1, 1990
Normal left ventricular performance in children with X-linked hypophosphatemic rickets: a Doppler echocardiography study
I Vered, Z Vered, J E Perez, et al.
Calcified Tissue International
|
March 14, 1998
Differing lumbar vertebral mineralization rates in ambulatory pediatric patients with osteogenesis imperfecta
W R Reinus, W H McAlister, F Schranck, et al.
Journal of Zoo and Wildlife Medicine : Official Publication of the American Association of Zoo Veterinarians
|
March 10, 2001
Management and prevention of vitamin D deficiency rickets in captive-born juvenile chimpanzees (Pan troglodytes)
R E Junge, F H Gannon, I Porton, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 15, 1992
Different missense mutations at the tissue-nonspecific alkaline phosphatase gene locus in autosomal recessively inherited forms of mild and severe hypophosphatasia
P S Henthorn, M Raducha, K N Fedde, et al.
The Journal of Clinical Investigation
|
July 1, 1990
Mapping the gene causing X-linked recessive idiopathic hypoparathyroidism to Xq26-Xq27 by linkage studies
R V Thakker, K E Davies, M P Whyte, et al.
Arthritis and Rheumatism
|
April 1, 1978
Idiopathic multicentric osteolysis. Report of an affected father and son
M P Whyte, W A Murphy, M Kleerekoper, et al.
Archives of Internal Medicine
|
November 1, 1984
Systemic mastocytosis
P E Korenblat, H J Wedner, M P Whyte, et al.
Page
of 17
Search research articles
Search
Showing results (91-100 of 166) with videos related to
Sort By:
Page
of 17
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
January 5, 2002
Preonset studies of spondyloepiphyseal dysplasia tarda caused by a novel 2-base pair deletion in SEDL encoding sedlin
S Mumm, X Zhang, G S Gottesman, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
October 1, 1996
Creatine kinase brain isoenzyme (BB-CK) presence in serum distinguishes osteopetroses among the sclerosing bone disorders
M P Whyte, A Chines, D P Silva, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 14, 1997
Extraskeletal osteoclastomas responsive to dexamethasone treatment in Paget bone disease
K Ziambaras, W A Totty, S L Teitelbaum, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
May 1, 1990
Normal left ventricular performance in children with X-linked hypophosphatemic rickets: a Doppler echocardiography study
I Vered, Z Vered, J E Perez, et al.
Calcified Tissue International
|
March 14, 1998
Differing lumbar vertebral mineralization rates in ambulatory pediatric patients with osteogenesis imperfecta
W R Reinus, W H McAlister, F Schranck, et al.
Journal of Zoo and Wildlife Medicine : Official Publication of the American Association of Zoo Veterinarians
|
March 10, 2001
Management and prevention of vitamin D deficiency rickets in captive-born juvenile chimpanzees (Pan troglodytes)
R E Junge, F H Gannon, I Porton, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 15, 1992
Different missense mutations at the tissue-nonspecific alkaline phosphatase gene locus in autosomal recessively inherited forms of mild and severe hypophosphatasia
P S Henthorn, M Raducha, K N Fedde, et al.
The Journal of Clinical Investigation
|
July 1, 1990
Mapping the gene causing X-linked recessive idiopathic hypoparathyroidism to Xq26-Xq27 by linkage studies
R V Thakker, K E Davies, M P Whyte, et al.
Arthritis and Rheumatism
|
April 1, 1978
Idiopathic multicentric osteolysis. Report of an affected father and son
M P Whyte, W A Murphy, M Kleerekoper, et al.
Archives of Internal Medicine
|
November 1, 1984
Systemic mastocytosis
P E Korenblat, H J Wedner, M P Whyte, et al.
Page
of 17