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Urine concentration impairment in sickle cell anemia: genuine nephrogenic diabetes insipidus or osmotic diuresis?

Am J Physiol Renal Physiol
de Berny Q, Saint-Jacques C, Santin A, Mattioni S, Steichen O, Chieze R, Frochot V, Letavernier E, Lionnet F, Haymann JP.   +9 more
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Nephrogenic Diabetes Insipidus

Advances in Chronic Kidney Disease, 1998
Nephrogenic diabetes insipidus (NDI), which can be inherited or acquired, is characterized by an inability to concentrate urine despite normal or elevated plasma concentrations of the antidiuretic hormone arginine vasopressin (AVP). Polyuria, with hyposthenuria, and polydipsia are the cardinal clinical manifestations of the disease.
S E, DICKER, M G, EGGLETON
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Nephrogenic diabetes insipidus

Current Opinion in Nephrology and Hypertension, 2000
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Deen, P.M.T., Marr, N., Kamsteeg, E.J., Balkom, B.W.M. van   +3 more
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Nephrogenic Diabetes Insipidus

Pediatrics In Review, 1996
Nephrogenic diabetes insipidus (NDI) is a disorder, either congenital or acquired, in which antidiuretic hormone (ADH) secretion is normal, but the ability to concentrate urine is reduced because of insensitivity of the collecting tubule to ADH. The antidiuretic action of arginine vasopressin requires binding of the hormone to the renal type V2 ...
J, FABIAN, V, DUFEK
openaire   +4 more sources