Works matching IS 03000664 AND DT 1998 AND VI 49 AND IP 6
Results: 17
Aldosterone production despite absence or defectiveness of the CYP21 genes in two patients with salt-losing congenital adrenal hyperplasia caused by steroid 21-hydroxylase deficiency.
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- Clinical Endocrinology, 1998, v. 49, n. 6, p. 815, doi. 10.1046/j.1365-2265.1998.00431.x
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- Article
Hormonal aspects of epithelial ovarian cancer: review of epidemiological evidence.
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- Clinical Endocrinology, 1998, v. 49, n. 6, p. 695, doi. 10.1046/j.1365-2265.1998.00577.x
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The efficacy of DDAVP is related to the circadian rhythm of urine output in patients with persisting nocturnal enuresis.
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- Clinical Endocrinology, 1998, v. 49, n. 6, p. 793, doi. 10.1046/j.1365-2265.1998.00587.x
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Growth in children with craniopharyngioma following surgery.
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- Clinical Endocrinology, 1998, v. 49, n. 6, p. 733, doi. 10.1046/j.1365-2265.1998.00590.x
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Recombinant human insulin-like growth factor-I (rhIGF-I) therapy in adults with type 1 diabetes mellitus: effects on IGFs, IGF-binding proteins, glucose levels and insulin treatment.
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- Clinical Endocrinology, 1998, v. 49, n. 6, p. 739, doi. 10.1046/j.1365-2265.1998.00600.x
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Effects of growth hormone treatment on serum levels of insulin-like growth factors (IGFs) and IGF binding proteins 1–4 in postmenopausal women.
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- Clinical Endocrinology, 1998, v. 49, n. 6, p. 747, doi. 10.1046/j.1365-2265.1998.00606.x
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Screening for primary aldosteronism with a logistic multivariate discriminant analysis.
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- Clinical Endocrinology, 1998, v. 49, n. 6, p. 713, doi. 10.1046/j.1365-2265.1998.00608.x
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Comparison of the diagnostic utility of the simplified and standard i.m. glucagon stimulation test (IMGST).
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- Clinical Endocrinology, 1998, v. 49, n. 6, p. 773, doi. 10.1046/j.1365-2265.1998.00610.x
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Secondary adrenal insufficiency associated with autoimmune disorders: a report of twenty-five cases.
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- Clinical Endocrinology, 1998, v. 49, n. 6, p. 779, doi. 10.1046/j.1365-2265.1998.00611.x
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The IGF-I response to very low rhGH doses is preserved in human ageing.
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- Clinical Endocrinology, 1998, v. 49, n. 6, p. 757, doi. 10.1046/j.1365-2265.1998.00613.x
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The effects of oestrogen exposure on bone mass in male to female transsexuals.
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- Clinical Endocrinology, 1998, v. 49, n. 6, p. 811, doi. 10.1046/j.1365-2265.1998.00614.x
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Decreased regional blood flow in patients with acromegaly.
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- Clinical Endocrinology, 1998, v. 49, n. 6, p. 725, doi. 10.1046/j.1365-2265.1998.00620.x
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Dual facets of hyponatraemia and arginine vasopressin in patients with ACTH deficiency.
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- Clinical Endocrinology, 1998, v. 49, n. 6, p. 785, doi. 10.1046/j.1365-2265.1998.00621.x
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Conn's syndrome: no longer a needle in a haystack?
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- Clinical Endocrinology, 1998, v. 49, n. 6, p. 709, doi. 10.1046/j.1365-2265.1998.00623.x
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Serum oestradiol and oestrogen-receptor gene polymorphism are associated with bone mineral density independently of serum testosterone in normal males.
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- Clinical Endocrinology, 1998, v. 49, n. 6, p. 803, doi. 10.1046/j.1365-2265.1998.00631.x
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One-year follow-up of quality of life in adults with untreated growth hormone deficiency.
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- Clinical Endocrinology, 1998, v. 49, n. 6, p. 765, doi. 10.1046/j.1365-2265.1998.00634.x
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Heterogeneous haemodynamics in acromegaly: evidence of endothelial dysfunction?
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- Clinical Endocrinology, 1998, v. 49, n. 6, p. 711, doi. 10.1046/j.1365-2265.1998.00646.x
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