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[Nephrogenic diabetes insipidus].

Boletin medico del Hospital Infantil de Mexico
The anti-diuretic hormone arginine-vasopressin (AVP) is released from the pituitary and regulates water reabsorption in the principal cells of the kidney collecting duct. Binding of AVP to the arginine-vasopressin receptor type-2 in the basolateral membrane leads to translocation of aquaporin-2 water channels to the apical membrane of the principal ...
Luis, Velásquez-Jones, Mara, Medeiros-Domingo   +1 more
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Nephrogenic Diabetes Insipidus [PDF]

, 2020
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[Nephrogenic diabetes insipidus].

Pediatria polska, 1972
A, Radzikowski, T, Zalewski, A, Milanowski   +2 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
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Nephrogenic Diabetes Insipidus

Radiology, 1966
The urographic picture of marked generalized dilatation of the urinary collecting system can present a challenging problem to both the radiologist and the referring clinician. The possible causes are numerous. The frequent occurrence of mild-to-moderate bilateral hydroureter and hydronephrosis during pregnancy or as a consequence of long-standing ...
S S, Miller, M C, Winston
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NEPHROGENIC DIABETES INSIPIDUS

Pediatrics, 1955
1. Two cases of congenital diabetes insipidus resistant to pitressin, or diabetes insipidus of the nephrogenic type, occurring in male cousins during infancy have been described in which the most striking manifestations were recurrent pyrexia, polyuria, polydipsia, poor weight gain and development and hyperelectrolytemia. 2.
J R, WEST, J G, KRAMER
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Nephrogenic Diabetes Insipidus

Annual Review of Physiology, 2001
▪ Abstract  Nephrogenic diabetes insipidus, 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. Polyuria, with hyposthenuria, and polydipsia are the cardinal clinical manifestations of the disease.
J P, Morello, D G, Bichet
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Nephrogenic Diabetes Insipidus

2009
Publisher Summary This chapter provides details on the role of aquaporin-2 (AQP2), the AVP-dependent water channel of the collecting duct, in several diseases. Arginine vasopressin (AVP) is the hormone that controls serum osmolality by decreasing free water clearance; any condition that interferes with AVP production, secretion and binding to V2 ...
Nine V. A. M. Knoers, Elena N. Levtchenko   +1 more
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