Buscar
Mostrando ítems 1-10 de 14
Potentially dangerous effect of disopyramide on atrioventricular conduction in a patient on digitalis
(British Medical Journal, 1980)
Determination of thin surface layers in-situ by the conversion electron mössbauer spectroscopy /CEMS/, using a parallel plate avalanche counter /PPAC/
(Journal of Radioanalytical and Nuclear Chemistry, 1988)
In the present paper we describe a technique for the determination of thin layer thicknesses by the conversion electron Mössbauer spectroscopy /CEMS/, using a new alternative method, a parallel plate avalanche counter ...
Hormonal evaluation of a large kindred with complete androgen insensitivity: evidence for secondary 5α-reductase deficiency.
(The Journal of Clinical Endocrinology & Metabolism, 1982-05)
Seventeen individuals from a pedigree with complete androgen insensitivity, [testicular feminization (TF)] are presented. Their hormonal evaluation was compared with those of normal males and male pseudohermaphrodites with ...
Urinary steroid metabolites in subjects with male pseudohermaphroditism due to 5α-reductase deficiency
(Wiley, 1985-07)
To investigate the enzymatic basis for abnormal steroid metabolism in subjects with male pseudohermaphroditism due to 5α-reductase deficiency, the ring A reduced urinary 5β and 5α metabolites of testosterone, androstenedione, ...
Testicular function in 2 cases of penile agenesis
(The Journal of Urology, 1981-10-05)
Two cases of congenital absence of the penis are presented. In both cases testicular androgen function was adequate, as judged by measurements of plasma androgens after administration of human chorionic gonadotropin
Male pseudohermaphroditism due to multiple defects in steroid-biosynthetic microsomal mixed-function oxidases — a new variant of congenital adrenal hyperplasia
(New England Journal of Medicine, 1985-11-07)
A six-month-old 46,XY infant with a female phenotype and ambiguous genitalia was evaluated for male pseudohermaphroditism. The principal findings were (1) low basal plasma levels of all measured C19 steroids and their ...
Decreased Urinary C19 and C21 Steroid 5α-Metabolites in Parents of Male Pseudohermaphrodites with 5α- Reductase Deficiency: Detection of Carriers
(The Journal of Clinical Endocrinology & Metabolism, 1985-05-01)
The urinary 5β/5α ring A-reduced metabolites of C19 and C12 steroids from obligate carrier parents of male) pseudohermaphrodites with 5a-reductase deficiency were analyzed by gas chromatography. Etiocholanolone/androsterone, ...
Reversibility of catecholamine-induced dilated cardiomyopathy in a child with a pheochromocytoma
(N Engl J Med, 1987-03-26)
Patients with a severe, dilated cardiomyopathy with congestive heart failure have a poor prognosis unless a correctable cause can be identified. Even when a cause is found, the degree of reversibility of myocardial injury ...
Inherited 5α-reductase deficiency in man
(ScienceDirect, 1986)
Study of the syndrome of 5α-reductase deficiency in man has elucidated the importance of testosterone conversion to dihydrotestosterone in sexual differentiation of the male fetus. Insights into specific actions for ...
A low-cost LN2 monitor
(American Journal of Physician, 1989)