17-ketosteroids has been researched along with Hyperkalemia* in 10 studies
10 other study(ies) available for 17-ketosteroids and Hyperkalemia
| Article | Year |
|---|---|
Partial 3 -hydroxysteroid dehydrogenase (3 -HSD) deficiency in a family with congenital adrenal hyperplasia: evidence for increasing 3 -HSD activity with age.
Topics: 17-Hydroxycorticosteroids; 17-Ketosteroids; Adrenal Gland Diseases; Aging; Aldosterone; Androstanes; Androsterone; Child; Child, Preschool; Chlorides; Chromatography, Gas; Chromatography, Thin Layer; Dehydroepiandrosterone; Disorders of Sex Development; Etiocholanolone; Female; Glucuronates; Humans; Hydrocortisone; Hydroxysteroid Dehydrogenases; Hyperkalemia; Hyperplasia; Hyponatremia; Infant; Infant, Newborn; Male; Metabolism, Inborn Errors; Potassium; Pregnanetriol; Pregnenolone; Sodium; Sulfates; Testosterone | 1971 |
Selective aldosterone deficiency.
Topics: 17-Ketosteroids; Adolescent; Adrenal Insufficiency; Aged; Aldosterone; Aminohippuric Acids; Carbon Isotopes; Chlorothiazide; Chromatography, Paper; Desoxycorticosterone; Diagnosis, Differential; Diet Therapy; Female; Glomerular Filtration Rate; Glucocorticoids; Heart Failure; Humans; Hyperkalemia; Inulin; Kidney; Male; Metabolism, Inborn Errors; Middle Aged; Mixed Function Oxygenases; Organomercury Compounds; Potassium; Regional Blood Flow; Sodium; Water-Electrolyte Balance | 1969 |
Ventricular tachycardia associated with hyperkalemia. Occurrence in an infant aged 13 days with adrenogenital syndrome.
Topics: 17-Hydroxycorticosteroids; 17-Ketosteroids; Adrenal Hyperplasia, Congenital; Electrocardiography; Humans; Hyperkalemia; Infant, Newborn; Infant, Newborn, Diseases; Male; Pregnanetriol; Tachycardia | 1969 |
[Long term development of adrenal gland insufficiency, designated regressive, in newborn infants].
Topics: 17-Hydroxycorticosteroids; 17-Ketosteroids; Adrenal Cortex Hormones; Adrenal Insufficiency; Aldosterone; Body Height; Body Weight; Child; Child, Preschool; Dehydration; Female; Fluorometry; Humans; Hydrocortisone; Hyperkalemia; Infant; Infant, Newborn; Infant, Newborn, Diseases; Male; Melanins; Pigmentation Disorders; Seizures; Sodium Chloride; Time Factors | 1969 |
Cortisol production rate. V. Congenital virilizing adrenal hyperplasia.
Topics: 17-Ketosteroids; Adolescent; Adrenal Hyperplasia, Congenital; Adrenocorticotropic Hormone; Child; Child, Preschool; Cortisone; Electrolytes; Female; Humans; Hydrocortisone; Hyperkalemia; Hyponatremia; Infant; Infant, Newborn; Male; Mineralocorticoids; Mixed Function Oxygenases; Potassium; Sodium; Virilism | 1966 |
Hyperaldosteronism, hyperplasia of the juxtaglomerular complex, normal blood pressure, and dwarfism: report of a case.
Topics: 17-Hydroxycorticosteroids; 17-Ketosteroids; Adrenalectomy; Alkalosis; Child; Dwarfism; Female; Humans; Hyperaldosteronism; Hyperkalemia; Hyperplasia; Juxtaglomerular Apparatus; Photometry | 1966 |
FAMILIAL HYPERKALEMIC PERIODIC PARALYSIS WITH MYOTONIC FEATURES.
Topics: 17-Ketosteroids; Acetazolamide; Adolescent; Biopsy; Blood Chemical Analysis; Child; Dextroamphetamine; Epinephrine; Geriatrics; Humans; Hydrogen-Ion Concentration; Hyperkalemia; Muscles; Myotonia; Paralyses, Familial Periodic; Paralysis; Paralysis, Hyperkalemic Periodic; Sodium; Spironolactone; Sweat; Urine; Water-Electrolyte Balance | 1964 |
SIMMONDS-SHEEHAN'S SYNDROME. A CLINICAL SURVEY OF 100 CASES.
Topics: 17-Ketosteroids; Adolescent; Adrenal Cortex Hormones; Anemia; Arrhythmias, Cardiac; Body Temperature; Bradycardia; Carbohydrate Metabolism; Cardiomegaly; China; Electrocardiography; Geriatrics; Hair; Humans; Hyperkalemia; Hyponatremia; Hypopituitarism; Pigmentation; Thyroid Function Tests | 1964 |
ISOLATED ANALDOSTERONISM. I. CLINICAL ENTITY, WITH MANIFESTATIONS OF PERSISTENT HYPERKALEMIA, PERIODIC PARALYSIS, SALT-LOSING TENDENCY, AND ACIDOSIS.
Topics: 17-Hydroxycorticosteroids; 17-Ketosteroids; Acidosis; Adolescent; Adrenocorticotropic Hormone; Chromatography; Deficiency Diseases; Diet; Electrocardiography; Humans; Hyperkalemia; Hyponatremia; Muscular Diseases; Paralysis; Sodium Chloride; Urine; Water-Electrolyte Balance | 1964 |
A NEW HEREDITARY DEFECT IN THE BIOSYNTHESIS OF ALDOSTERONE: URINARY C21-CORTICOSTEROID PATTERN IN THREE RELATED PATIENTS WITH A SALT-LOSING SYNDROME, SUGGESTING AN 18-OXIDATION DEFECT.
Topics: 17-Hydroxycorticosteroids; 17-Ketosteroids; Adolescent; Adrenal Cortex Hormones; Adrenocorticotropic Hormone; Aldosterone; Birth Order; Consanguinity; Desoxycorticosterone; Genetics, Medical; Humans; Hyperkalemia; Hyponatremia; Infant; Metabolism, Inborn Errors; Pathology; Sex; Syndrome | 1964 |