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M P Whyte

Showing results (121-130 of 166) with videos related to

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Medicine|January 1, 1984
Hypophosphatasia: clinicopathologic comparison of the infantile, childhood, and adult formsM D Fallon, S L Teitelbaum, R S Weinstein, et al.
Journal of Inherited Metabolic Disease|February 22, 2000
Increased urine heparan and chondroitin sulphate excretion in patients with osteopetrosisR D Steiner, M P Whyte, E Chang, et al.
Pediatric Radiology|May 1, 1997
Metachondromatosis: report of a family with facial features mildly resembling trichorhinophalangeal syndromePediatr Radiol 1997 Nov;27(11):864T E Herman, A Chines, W H McAlister, et al.
Connective Tissue Research|January 1, 1989
First identification of a gene defect for hypophosphatasia: evidence that alkaline phosphatase acts in skeletal mineralizationM J Weiss, D E Cole, K Ray, et al.
Experimental Hematology|October 12, 1999
Measles virus nucleocapsid transcript expression is not restricted to the osteoclast lineage in patients with Paget's disease of boneS V Reddy, C Menaa, F R Singer, et al.
The Journal of Clinical Investigation|April 1, 1988
Perinatal hypophosphatasia: tissue levels of vitamin B6 are unremarkable despite markedly increased circulating concentrations of pyridoxal-5'-phosphate. Evidence for an ectoenzyme role for tissue-nonspecific alkaline phosphataseM P Whyte, J D Mahuren, K N Fedde, et al.
Medicine|November 1, 1989
X-linked hypophosphatemia: a clinical, biochemical, and histopathologic assessment of morbidity in adultsI R Reid, D C Hardy, W A Murphy, et al.
The New England Journal of Medicine|April 10, 1986
Increased serum pyridoxal-5'-phosphate in pseudohypophosphatasiaD E Cole, S R Salisbury, R A Stinson, et al.
The American Journal of Medicine|January 1, 1991
X-linked hypophosphatemia: skeletal mass in adults assessed by histomorphometry, computed tomography, and absorptiometryI R Reid, W A Murphy, D C Hardy, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1988
A missense mutation in the human liver/bone/kidney alkaline phosphatase gene causing a lethal form of hypophosphatasiaM J Weiss, D E Cole, K Ray, et al.
Pageof 17

Showing results (121-130 of 166) with videos related to

Sort By:
Pageof 17
Medicine|January 1, 1984
Hypophosphatasia: clinicopathologic comparison of the infantile, childhood, and adult formsM D Fallon, S L Teitelbaum, R S Weinstein, et al.
Journal of Inherited Metabolic Disease|February 22, 2000
Increased urine heparan and chondroitin sulphate excretion in patients with osteopetrosisR D Steiner, M P Whyte, E Chang, et al.
Pediatric Radiology|May 1, 1997
Metachondromatosis: report of a family with facial features mildly resembling trichorhinophalangeal syndromePediatr Radiol 1997 Nov;27(11):864T E Herman, A Chines, W H McAlister, et al.
Connective Tissue Research|January 1, 1989
First identification of a gene defect for hypophosphatasia: evidence that alkaline phosphatase acts in skeletal mineralizationM J Weiss, D E Cole, K Ray, et al.
Experimental Hematology|October 12, 1999
Measles virus nucleocapsid transcript expression is not restricted to the osteoclast lineage in patients with Paget's disease of boneS V Reddy, C Menaa, F R Singer, et al.
The Journal of Clinical Investigation|April 1, 1988
Perinatal hypophosphatasia: tissue levels of vitamin B6 are unremarkable despite markedly increased circulating concentrations of pyridoxal-5'-phosphate. Evidence for an ectoenzyme role for tissue-nonspecific alkaline phosphataseM P Whyte, J D Mahuren, K N Fedde, et al.
Medicine|November 1, 1989
X-linked hypophosphatemia: a clinical, biochemical, and histopathologic assessment of morbidity in adultsI R Reid, D C Hardy, W A Murphy, et al.
The New England Journal of Medicine|April 10, 1986
Increased serum pyridoxal-5'-phosphate in pseudohypophosphatasiaD E Cole, S R Salisbury, R A Stinson, et al.
The American Journal of Medicine|January 1, 1991
X-linked hypophosphatemia: skeletal mass in adults assessed by histomorphometry, computed tomography, and absorptiometryI R Reid, W A Murphy, D C Hardy, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1988
A missense mutation in the human liver/bone/kidney alkaline phosphatase gene causing a lethal form of hypophosphatasiaM J Weiss, D E Cole, K Ray, et al.
Pageof 17