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M P Whyte

Showing results (71-80 of 166) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|November 14, 1997
Calcinosis universalis complicating juvenile dermatomyositis: resolution during probenecid therapyM C Eddy, R Leelawattana, W H McAlister, et al.
Transactions of the Association of American Physicians|January 1, 1978
Adult hypophosphatasia dominant inheritance in a large kindredM P Whyte, S L Teitelbaum, W A Murphy, et al.
The Journal of Clinical Endocrinology and Metabolism|July 1, 1996
Aberrant properties of alkaline phosphatase in patient fibroblasts correlate with clinical expressivity in severe forms of hypophosphatasiaK N Fedde, M P Michell, P S Henthorn, et al.
Skeletal Radiology|January 1, 1981
Mixed-sclerosing-bone-dystrophy: report of a case and review of the literatureM P Whyte, W A Murphy, M D Fallon, et al.
The American Journal of Medicine|December 1, 1981
Axial osteomalacia. Clinical, laboratory and genetic investigation of an affected mother and sonM P Whyte, M D Fallon, W A Murphy, et al.
Clinical Chemistry|June 1, 1980
Hypophosphatasia (adult form): quantitation of serum alkaline phosphatase isoenzyme activity in a large kindredJ L Millán, M P Whyte, L V Avioli, et al.
American Journal of Medical Genetics|May 30, 1998
Bilateral radial ray hypoplasia with multiple epiphyseal dysplasiaM C Eddy, R D Steiner, W H McAlister, et al.
International Review of Physiology|January 1, 1981
Hormonal regulation of mineral metabolismS J Birge, T J Hahn, M P Whyte, et al.
The Journal of Clinical Endocrinology and Metabolism|February 1, 1982
Normal cortical bone mass in patients after long term coumadin therapyL D Piro, M P Whyte, W A Murphy, et al.
Medicine|February 17, 1999
X-linked recessive spondyloepiphyseal dysplasia tarda. Clinical and radiographic evolution in a 6-generation kindred and review of the literatureM P Whyte, G S Gottesman, M C Eddy, et al.
Pageof 17

Showing results (71-80 of 166) with videos related to

Sort By:
Pageof 17
The Journal of Clinical Endocrinology and Metabolism|November 14, 1997
Calcinosis universalis complicating juvenile dermatomyositis: resolution during probenecid therapyM C Eddy, R Leelawattana, W H McAlister, et al.
Transactions of the Association of American Physicians|January 1, 1978
Adult hypophosphatasia dominant inheritance in a large kindredM P Whyte, S L Teitelbaum, W A Murphy, et al.
The Journal of Clinical Endocrinology and Metabolism|July 1, 1996
Aberrant properties of alkaline phosphatase in patient fibroblasts correlate with clinical expressivity in severe forms of hypophosphatasiaK N Fedde, M P Michell, P S Henthorn, et al.
Skeletal Radiology|January 1, 1981
Mixed-sclerosing-bone-dystrophy: report of a case and review of the literatureM P Whyte, W A Murphy, M D Fallon, et al.
The American Journal of Medicine|December 1, 1981
Axial osteomalacia. Clinical, laboratory and genetic investigation of an affected mother and sonM P Whyte, M D Fallon, W A Murphy, et al.
Clinical Chemistry|June 1, 1980
Hypophosphatasia (adult form): quantitation of serum alkaline phosphatase isoenzyme activity in a large kindredJ L Millán, M P Whyte, L V Avioli, et al.
American Journal of Medical Genetics|May 30, 1998
Bilateral radial ray hypoplasia with multiple epiphyseal dysplasiaM C Eddy, R D Steiner, W H McAlister, et al.
International Review of Physiology|January 1, 1981
Hormonal regulation of mineral metabolismS J Birge, T J Hahn, M P Whyte, et al.
The Journal of Clinical Endocrinology and Metabolism|February 1, 1982
Normal cortical bone mass in patients after long term coumadin therapyL D Piro, M P Whyte, W A Murphy, et al.
Medicine|February 17, 1999
X-linked recessive spondyloepiphyseal dysplasia tarda. Clinical and radiographic evolution in a 6-generation kindred and review of the literatureM P Whyte, G S Gottesman, M C Eddy, et al.
Pageof 17