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Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
March 7, 2000
Polycystic bone disease
M P Whyte, M C Eddy, M N Podgornik, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
August 24, 1999
Polycystic bone disease: A new, autosomal dominant disorder
M P Whyte, M C Eddy, M N Podgornik, et al.
The Journal of Clinical Endocrinology and Metabolism
|
June 1, 1979
Vitamin D bioavailability: serum 25-hydroxyvitamin D levels in man after oral, subcutaneous, intramuscular, and intravenous vitamin D administration
M P Whyte, J G Haddad, D D Walters, et al.
The Journal of Clinical Investigation
|
August 1, 1985
Markedly increased circulating pyridoxal-5'-phosphate levels in hypophosphatasia. Alkaline phosphatase acts in vitamin B6 metabolism
M P Whyte, J D Mahuren, L A Vrabel, et al.
The Journal of Pediatrics
|
January 1, 1986
Infantile hypophosphatasia: normalization of circulating bone alkaline phosphatase activity followed by skeletal remineralization. Evidence for an intact structural gene for tissue nonspecific alkaline phosphatase
M P Whyte, H L Magill, M D Fallon, et al.
Arthritis and Rheumatism
|
March 1, 1997
Surgical management of calcinosis cutis universalis in systemic lupus erythematosus
M A Cousins, D B Jones, M P Whyte, et al.
Calcified Tissue International
|
January 1, 1983
Mast-cell proliferation in postmenopausal osteoporosis
M D Fallon, M P Whyte, R B Craig, et al.
The Annals of Otology, Rhinology, and Laryngology
|
July 1, 1986
Audiologic findings in young patients with hypophosphatemic bone disease
M Meister, A Johnson, G R Popelka, et al.
The American Journal of Medicine
|
April 1, 1989
Normal left ventricular performance documented by Doppler echocardiography in patients with long-standing hypocalcemia
I Vered, Z Vered, J E Perez, et al.
American Journal of Human Genetics
|
January 1, 1997
mtDNA analysis shows common ancestry in two kindreds with X-linked recessive hypoparathyroidism and reveals a heteroplasmic silent mutation
S Mumm, M P Whyte, R V Thakker, et al.
Page
of 17
Search research articles
Search
Showing results (81-90 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
|
March 7, 2000
Polycystic bone disease
M P Whyte, M C Eddy, M N Podgornik, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
August 24, 1999
Polycystic bone disease: A new, autosomal dominant disorder
M P Whyte, M C Eddy, M N Podgornik, et al.
The Journal of Clinical Endocrinology and Metabolism
|
June 1, 1979
Vitamin D bioavailability: serum 25-hydroxyvitamin D levels in man after oral, subcutaneous, intramuscular, and intravenous vitamin D administration
M P Whyte, J G Haddad, D D Walters, et al.
The Journal of Clinical Investigation
|
August 1, 1985
Markedly increased circulating pyridoxal-5'-phosphate levels in hypophosphatasia. Alkaline phosphatase acts in vitamin B6 metabolism
M P Whyte, J D Mahuren, L A Vrabel, et al.
The Journal of Pediatrics
|
January 1, 1986
Infantile hypophosphatasia: normalization of circulating bone alkaline phosphatase activity followed by skeletal remineralization. Evidence for an intact structural gene for tissue nonspecific alkaline phosphatase
M P Whyte, H L Magill, M D Fallon, et al.
Arthritis and Rheumatism
|
March 1, 1997
Surgical management of calcinosis cutis universalis in systemic lupus erythematosus
M A Cousins, D B Jones, M P Whyte, et al.
Calcified Tissue International
|
January 1, 1983
Mast-cell proliferation in postmenopausal osteoporosis
M D Fallon, M P Whyte, R B Craig, et al.
The Annals of Otology, Rhinology, and Laryngology
|
July 1, 1986
Audiologic findings in young patients with hypophosphatemic bone disease
M Meister, A Johnson, G R Popelka, et al.
The American Journal of Medicine
|
April 1, 1989
Normal left ventricular performance documented by Doppler echocardiography in patients with long-standing hypocalcemia
I Vered, Z Vered, J E Perez, et al.
American Journal of Human Genetics
|
January 1, 1997
mtDNA analysis shows common ancestry in two kindreds with X-linked recessive hypoparathyroidism and reveals a heteroplasmic silent mutation
S Mumm, M P Whyte, R V Thakker, et al.
Page
of 17