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M P Whyte

Showing results (111-120 of 166) with videos related to

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Medicine|September 1, 1979
Adult hypophosphatasia. Clinical, laboratory, and genetic investigation of a large kindred with review of the literatureM P Whyte, S L Teitelbaum, W A Murphy, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 1, 1992
X-linked hypophosphatemic rickets: a study (with literature review) of linear growth response to calcitriol and phosphate therapyD J Petersen, A M Boniface, F W Schranck, et al.
The American Journal of Pathology|December 24, 1997
Matrix vesicles in osteomalacic hypophosphatasia bone contain apatite-like mineral crystalsH C Anderson, H H Hsu, D C Morris, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1983
Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcificationW S Sly, D Hewett-Emmett, M P Whyte, et al.
Journal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|March 1, 1983
Serum total hydroxyproline assay: effects of age, sex and Paget's bone diseaseT J Gilbertson, M N Brunden, S B Gruszczyk, et al.
The Journal of Investigative Dermatology|April 1, 1981
Biochemical and ultrastructural demonstration of elastin accumulation in the skin lesions of the Buschke-Ollendorff syndromeJ Uitto, D J Santa Cruz, B C Starcher, et al.
Bone|January 1, 1988
Assessment of calcitriol and inorganic phosphate therapy before cure of oncogenous osteomalacia by resection of a mixed mesenchymal tumorH C Taylor, D Santa-Cruz, S L Teitelbaum, et al.
Clinical Endocrinology|December 1, 1996
Calcium-sensing receptor mutations in familial hypocalciuric hypercalcaemia with recurrent pancreatitisS H Pearce, C Wooding, M Davies, et al.
Biochemical and Biophysical Research Communications|February 24, 1997
Expression and cloning of the human X-linked hypophosphatemia gene cDNAM Grieff, S Mumm, P Waeltz, et al.
The Journal of Clinical Endocrinology and Metabolism|February 1, 1980
Effect of the menstrual cycle on calcium-regulating hormones in the normal young womanD T Baran, M P Whyte, M R Haussler, et al.
Pageof 17

Showing results (111-120 of 166) with videos related to

Sort By:
Pageof 17
Medicine|September 1, 1979
Adult hypophosphatasia. Clinical, laboratory, and genetic investigation of a large kindred with review of the literatureM P Whyte, S L Teitelbaum, W A Murphy, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 1, 1992
X-linked hypophosphatemic rickets: a study (with literature review) of linear growth response to calcitriol and phosphate therapyD J Petersen, A M Boniface, F W Schranck, et al.
The American Journal of Pathology|December 24, 1997
Matrix vesicles in osteomalacic hypophosphatasia bone contain apatite-like mineral crystalsH C Anderson, H H Hsu, D C Morris, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1983
Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcificationW S Sly, D Hewett-Emmett, M P Whyte, et al.
Journal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|March 1, 1983
Serum total hydroxyproline assay: effects of age, sex and Paget's bone diseaseT J Gilbertson, M N Brunden, S B Gruszczyk, et al.
The Journal of Investigative Dermatology|April 1, 1981
Biochemical and ultrastructural demonstration of elastin accumulation in the skin lesions of the Buschke-Ollendorff syndromeJ Uitto, D J Santa Cruz, B C Starcher, et al.
Bone|January 1, 1988
Assessment of calcitriol and inorganic phosphate therapy before cure of oncogenous osteomalacia by resection of a mixed mesenchymal tumorH C Taylor, D Santa-Cruz, S L Teitelbaum, et al.
Clinical Endocrinology|December 1, 1996
Calcium-sensing receptor mutations in familial hypocalciuric hypercalcaemia with recurrent pancreatitisS H Pearce, C Wooding, M Davies, et al.
Biochemical and Biophysical Research Communications|February 24, 1997
Expression and cloning of the human X-linked hypophosphatemia gene cDNAM Grieff, S Mumm, P Waeltz, et al.
The Journal of Clinical Endocrinology and Metabolism|February 1, 1980
Effect of the menstrual cycle on calcium-regulating hormones in the normal young womanD T Baran, M P Whyte, M R Haussler, et al.
Pageof 17