Search Results - "Couch, R M"
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Effect of bacille Calmette-Guérin vaccination on C-peptide secretion in children newly diagnosed with IDDM
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
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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3
Allgrove syndrome: an autosomal recessive syndrome of ACTH insensitivity, achalasia and alacrima
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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High incidence of IDDM over 6 years in Edmonton, Alberta, Canada
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
Published in The journal of clinical endocrinology and metabolism (01-09-1986)“…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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6
Kinetic analysis of inhibition of human adrenal steroidogenesis by ketoconazole
Published in The journal of clinical endocrinology and metabolism (01-09-1987)“…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
Published in The journal of clinical endocrinology and metabolism (01-02-1989)“…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
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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9
Early onset fatal cerebral edema in diabetic ketoacidosis
Published in Diabetes care (01-01-1991)Get full text
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10
An autosomal dominant form of adolescent multinodular goiter
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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Congenital hypothyroidism caused by defective iodide transport
Published in The Journal of pediatrics (01-06-1985)Get more information
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Prolonged remission of Cushing disease after treatment with cyproheptadine
Published in The Journal of pediatrics (01-06-1984)Get more information
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13
Rat ventral prostate chromatin. Effect of androgens on its chemical composition, physical properties, and template activity
Published in Biochemistry (Easton) (01-07-1973)Get full text
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14
Hepatic dysfunction in Alström disease
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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Syndrome of mental retardation, facial anomalies, hypopituitarism, and distal arthrogryposis in sibs
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
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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Androgen-stimulated labelling of chromosomal proteins by isolated prostate nuclei
Published in Experimental cell research (15-03-1973)Get more information
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Apparent postnatal onset of some manifestations of the Wiedemann-Beckwith syndrome
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
Published in The journal of clinical endocrinology and metabolism (01-06-2005)“…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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