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M P Whyte

Showing results (51-60 of 166) with videos related to

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Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|August 1, 1988
Transfusion of carbonic anhydrase-replete erythrocytes fails to correct the acidification defect in the syndrome of osteopetrosis, renal tubular acidosis, and cerebral calcification (carbonic anhydrase-II deficiency)M P Whyte, L L Hamm, W S Sly
The Journal of Clinical Endocrinology and Metabolism|January 22, 1998
Hepatitis C-associated osteosclerosis: late onset after blood transfusion in an elderly womanJ L Shaker, W R Reinus, M P Whyte
Bone|January 16, 1998
X-linked hypophosphatemia: normal renal function despite medullary nephrocalcinosis 25 years after transient vitamin D2-induced renal azotemiaM C Eddy, W H McAlister, M P Whyte
The Journal of Bone and Joint Surgery. American Volume|April 1, 1980
Progressive diaphyseal dysplasia (Engelmann's disease). Report of a sporadic case of the mild formM D Fallon, M P Whyte, W A Murphy
The Journal of Clinical Endocrinology and Metabolism|January 27, 1999
Hyperparathyroidism and increased serum IGF-binding protein-2 levels in hepatitis C-associated osteosclerosisJ L Shaker, B P Moore, M P Whyte
Radiology|February 1, 1987
Tibial bowing exacerbated by partial premature epiphyseal closure in sex-linked hypophosphatemic ricketsW H McAlister, G S Kim, M P Whyte
Skeletal Radiology|January 1, 1986
Macroepiphyseal dysplasia with symptomatic osteoporosis, wrinkled skin, and aged appearance: a presumed autosomal recessive conditionW H McAlister, J D Coe, M P Whyte
Genomics|September 23, 1997
Sequence analysis of 139 kb in Xp22.1 containing spermine synthase and the 5' region of PEXM Grieff, M P Whyte, R V Thakker, et al.
Pediatric Research|October 1, 1985
Positive renal response to intravenous acetazolamide in patients with carbonic anhydrase II deficiencyW S Sly, M P Whyte, T Krupin, et al.
American Journal of Medical Genetics|October 6, 1999
Mild hypophosphatasia mimicking severe osteogenesis imperfecta in utero: bent but not brokenR M Pauli, P Modaff, S L Sipes, et al.
Pageof 17

Showing results (51-60 of 166) with videos related to

Sort By:
Pageof 17
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|August 1, 1988
Transfusion of carbonic anhydrase-replete erythrocytes fails to correct the acidification defect in the syndrome of osteopetrosis, renal tubular acidosis, and cerebral calcification (carbonic anhydrase-II deficiency)M P Whyte, L L Hamm, W S Sly
The Journal of Clinical Endocrinology and Metabolism|January 22, 1998
Hepatitis C-associated osteosclerosis: late onset after blood transfusion in an elderly womanJ L Shaker, W R Reinus, M P Whyte
Bone|January 16, 1998
X-linked hypophosphatemia: normal renal function despite medullary nephrocalcinosis 25 years after transient vitamin D2-induced renal azotemiaM C Eddy, W H McAlister, M P Whyte
The Journal of Bone and Joint Surgery. American Volume|April 1, 1980
Progressive diaphyseal dysplasia (Engelmann's disease). Report of a sporadic case of the mild formM D Fallon, M P Whyte, W A Murphy
The Journal of Clinical Endocrinology and Metabolism|January 27, 1999
Hyperparathyroidism and increased serum IGF-binding protein-2 levels in hepatitis C-associated osteosclerosisJ L Shaker, B P Moore, M P Whyte
Radiology|February 1, 1987
Tibial bowing exacerbated by partial premature epiphyseal closure in sex-linked hypophosphatemic ricketsW H McAlister, G S Kim, M P Whyte
Skeletal Radiology|January 1, 1986
Macroepiphyseal dysplasia with symptomatic osteoporosis, wrinkled skin, and aged appearance: a presumed autosomal recessive conditionW H McAlister, J D Coe, M P Whyte
Genomics|September 23, 1997
Sequence analysis of 139 kb in Xp22.1 containing spermine synthase and the 5' region of PEXM Grieff, M P Whyte, R V Thakker, et al.
Pediatric Research|October 1, 1985
Positive renal response to intravenous acetazolamide in patients with carbonic anhydrase II deficiencyW S Sly, M P Whyte, T Krupin, et al.
American Journal of Medical Genetics|October 6, 1999
Mild hypophosphatasia mimicking severe osteogenesis imperfecta in utero: bent but not brokenR M Pauli, P Modaff, S L Sipes, et al.
Pageof 17