Search Results - "Couch, R M"

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  1. 1

    Effect of bacille Calmette-Guérin vaccination on C-peptide secretion in children newly diagnosed with IDDM by ELLIOTT, J. E, MARLIN, K. L, COUCH, R. M

    Published in Diabetes care (01-10-1998)
    “…Effect of bacille Calmette-Guérin vaccination on C-peptide secretion in children newly diagnosed with IDDM. J F Elliott , K L Marlin and R M Couch Department…”
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    Dissociation of cortisol and adrenal androgen secretion in poorly controlled insulin-dependent diabetes mellitus by Couch, R M

    Published in Acta endocrinologica (Copenhagen) (01-08-1992)
    “…In acute illness, cortisol secretion increases whereas that of the adrenal androgens, dehydroepiandrosterone and dehydroepiandrosterone sulfate declines. The…”
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    Allgrove syndrome: an autosomal recessive syndrome of ACTH insensitivity, achalasia and alacrima by Moore, P S, Couch, R M, Perry, Y S, Shuckett, E P, Winter, J S

    Published in Clinical endocrinology (Oxford) (01-02-1991)
    “…Allgrove syndrome (isolated glucocorticoid deficiency, achalasia and alacrima) was found in eight members of an inbred French Canadian/North American Indian…”
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  4. 4

    High incidence of IDDM over 6 years in Edmonton, Alberta, Canada by TOTH, E. L, LEE, K.-C, COUCH, R. M, MARTIN, L. F

    Published in Diabetes care (01-03-1997)
    “…High incidence of IDDM over 6 years in Edmonton, Alberta, Canada. E L Toth , K C Lee , R M Couch and L F Martin Department of Medicine, University of Alberta,…”
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    Regulation of the activities of 17-hydroxylase and 17,20-desmolase in the human adrenal cortex: kinetic analysis and inhibition by endogenous steroids by Couch, R M, Muller, J, Winter, J S

    “…Kinetic analyses of 17-hydroxylase and 17,20-desmolase activities have been performed on human adrenal microsomes from 12 individuals, aged 1-60 yr. The median…”
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    Kinetic analysis of inhibition of human adrenal steroidogenesis by ketoconazole by Couch, R M, Muller, J, Perry, Y S, Winter, J S

    “…The kinetics of the inhibitory effects of the imidazole antimicrobial ketoconazole on the activities of the steroidogenic enzymes distal to cholesterol…”
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    Combined 17-hydroxylase and 17,20-desmolase deficiencies: evidence for synthesis of a defective cytochrome P450c17 by Winter, J S, Couch, R M, Muller, J, Perry, Y S, Ferreira, P, Baydala, L, Shackleton, C H

    “…We studied in vivo and in vitro steroidogenesis in six phenotypic female children with 17-hydroxylase deficiency. The diagnosis was suspected as a likely cause…”
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    A novel point mutation of thyroid hormone receptor beta gene in a family with resistance to thyroid hormone by Nagashima, T, Yagi, H, Nagashima, K, Sakurai, A, Onigata, K, Nomura, Y, Morikawa, A, Matazow, G, Couch, R M, Weiss, R E, Refetoff, S

    Published in Thyroid (New York, N.Y.) (01-10-1997)
    “…Resistance to thyroid hormone (RTH) is characterized by variable tissue hyporesponsiveness to thyroid hormone caused by mutations of thyroid hormone receptor…”
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    An autosomal dominant form of adolescent multinodular goiter by COUCH, R. M, HUGHES, I. A, DESA, D. J, SCHIFFRIN, A, GUYDA, H, WINTER, J. S. D

    Published in American journal of human genetics (01-12-1986)
    “…Eighteen members of an extended pedigree have been found to have a form of euthyroid adolescent multinodular goiter. Histological examination showed multiple…”
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    Hepatic dysfunction in Alström disease by Connolly, M B, Jan, J E, Couch, R M, Wong, L T, Dimmick, J E, Rigg, J M

    Published in American journal of medical genetics (15-09-1991)
    “…Alström disease is a rare disorder; less than 20 cases have been reported. An 11-year-old girl is described with this condition. She has pigmentary…”
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  15. 15

    Syndrome of mental retardation, facial anomalies, hypopituitarism, and distal arthrogryposis in sibs by Chitayat, D, Hall, J G, Couch, R M, Phang, M S, Baldwin, V J

    Published in American journal of medical genetics (01-09-1990)
    “…A brother and a sister presented with a malformation syndrome consisting of facial anomalies, distal arthrogryposis with camptodactyly of fingers and "hammer…”
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    Growth Hormone Supplementation and Psychosocial Functioning to Adult Height in Turner Syndrome: A Questionnaire Study of Participants in the Canadian Randomized Trial by Rovet, Joanne F, Van Vliet, Guy

    Published in Frontiers in endocrinology (Lausanne) (13-03-2019)
    “…Despite the long-held belief that growth hormone supplementation provides psychosocial benefits to patients with Turner syndrome (TS), this assumption has…”
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    Apparent postnatal onset of some manifestations of the Wiedemann-Beckwith syndrome by Chitayat, D, Rothchild, A, Ling, E, Friedman, J M, Couch, R M, Yong, S L, Baldwin, V J, Hall, J G

    Published in American journal of medical genetics (01-08-1990)
    “…We report on 2 patients who were apparently normal at birth but later developed characteristics of Wiedemann-Beckwith syndrome (WBS). Both had hypoglycemia…”
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    Impact of Growth Hormone Supplementation on Adult Height in Turner Syndrome: Results of the Canadian Randomized Controlled Trial by Stephure, David K

    “…Background: A randomized, controlled trial of GH supplementation to adult height in girls with short stature due to Turner syndrome was conducted in Canada. We…”
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