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T M Reade

Showing results (1-10 of 11) with videos related to

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Pediatrics|December 1, 1981
Outcome of early and long-term management of classical maple syrup urine diseaseC L Clow, T M Reade, C R Scriver
American Journal of Medical Genetics|August 1, 1987
Audiometric evidence for two forms of X-linked hypophosphatemia in humans, apparent counterparts of Hyp and Gy mutations in mouseA Boneh, T M Reade, C R Scriver, et al.
Oral Surgery, Oral Medicine, and Oral Pathology|September 1, 1988
Oral findings in patients with autosomal dominant hypophosphatemic bone disease and X-linked hypophosphatemia: further evidence that they are different diseasesS Schwartz, C R Scriver, T M Reade, et al.
The New England Journal of Medicine|November 2, 1978
Serum 1,25-dihydroxyvitamin D levels in normal subjects and in patients with hereditary rickets or bone diseaseC R Scriver, T M Reade, H F DeLuca, et al.
The Journal of Pediatrics|November 1, 1987
Nephrocalcinosis and its relationship to treatment of hereditary ricketsP R Goodyer, J B Kronick, S Jequier, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 1983
Serum osteocalcin in the treatment of inherited rickets with 1,25-dihydroxyvitamin D3C M Gundberg, D E Cole, J B Lian, et al.
The Journal of Pediatrics|March 1, 1985
Ontogeny modifies manifestations of cystinuria genes: implications for counselingC R Scriver, C L Clow, T M Reade, et al.
Pediatric Research|July 1, 1975
Response to crystalline 1alpha-hydroxyvitamin D3 in vitamin D dependencyT M Reade, C R Scriver, F H Glorieux, et al.
American Journal of Human Genetics|May 1, 1987
The Hartnup phenotype: Mendelian transport disorder, multifactorial diseaseC R Scriver, B Mahon, H L Levy, et al.
American Journal of Medical Genetics|April 1, 1983
Panostotic fibrous dysplasia: a congenital disorder of bone with unusual facial appearance, bone fragility, hyperphosphatasemia, and hypophosphatemiaD E Cole, F C Fraser, F H Glorieux, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Pediatrics|December 1, 1981
Outcome of early and long-term management of classical maple syrup urine diseaseC L Clow, T M Reade, C R Scriver
American Journal of Medical Genetics|August 1, 1987
Audiometric evidence for two forms of X-linked hypophosphatemia in humans, apparent counterparts of Hyp and Gy mutations in mouseA Boneh, T M Reade, C R Scriver, et al.
Oral Surgery, Oral Medicine, and Oral Pathology|September 1, 1988
Oral findings in patients with autosomal dominant hypophosphatemic bone disease and X-linked hypophosphatemia: further evidence that they are different diseasesS Schwartz, C R Scriver, T M Reade, et al.
The New England Journal of Medicine|November 2, 1978
Serum 1,25-dihydroxyvitamin D levels in normal subjects and in patients with hereditary rickets or bone diseaseC R Scriver, T M Reade, H F DeLuca, et al.
The Journal of Pediatrics|November 1, 1987
Nephrocalcinosis and its relationship to treatment of hereditary ricketsP R Goodyer, J B Kronick, S Jequier, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 1983
Serum osteocalcin in the treatment of inherited rickets with 1,25-dihydroxyvitamin D3C M Gundberg, D E Cole, J B Lian, et al.
The Journal of Pediatrics|March 1, 1985
Ontogeny modifies manifestations of cystinuria genes: implications for counselingC R Scriver, C L Clow, T M Reade, et al.
Pediatric Research|July 1, 1975
Response to crystalline 1alpha-hydroxyvitamin D3 in vitamin D dependencyT M Reade, C R Scriver, F H Glorieux, et al.
American Journal of Human Genetics|May 1, 1987
The Hartnup phenotype: Mendelian transport disorder, multifactorial diseaseC R Scriver, B Mahon, H L Levy, et al.
American Journal of Medical Genetics|April 1, 1983
Panostotic fibrous dysplasia: a congenital disorder of bone with unusual facial appearance, bone fragility, hyperphosphatasemia, and hypophosphatemiaD E Cole, F C Fraser, F H Glorieux, et al.
Pageof 2