Results 81 to 90 of about 1,031,173 (193)
Development of Genetically Engineered Mice Lacking All Three Nitric Oxide Synthases
Nitric oxide (NO) is produced in almost all tissues and organs, exerting multiple biological actions under both physiological and pathological conditions.
Masato Tsutsui +4 more
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Efficacy of COX-2 inhibitors in a case of congenital nephrogenic diabetes insipidus. [PDF]
A 17-month-old boy presented with failure to thrive, polyuria, and vomiting. He had been diagnosed clinically with nephrogenic diabetes insipidus and treated by amiloride and hydrochlorothiazide combination without a satisfactory outcome at another ...
Hoefsloot, L.H. +13 more
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X-Linked Recessive Form of Nephrogenic Diabetes Insipidus in A 7-Year-Old Boy
Nephrogenic diabetes insipidus (NDI) is caused by the inability of renal collecting duct cells to respond to arginine vasopressin (AVP)/antidiuretic hormone (ADH).
Janchevska A. +4 more
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Partial nephrogenic diabetes insipidus associated with Castleman’s disease
Background Nephrogenic diabetes insipidus (DI) secondary to a urinary tract obstruction is a rare condition. Herein, we report a case of partial nephrogenic DI due to obstructive uropathy in a patient with Castleman’s disease. Case presentation A 78-year-
Minah Kim +5 more
doaj +1 more source
Feeding disorders of infancy are common in paediatric practice. Among rare causes of this disturbance is diabetes insipidus (DI), which is a clinical syndrome characterized by polyuria, polydypsia and dehydration with hypernatraemia.
Katarzyna Anna Banasiak +6 more
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Type 1 Bartter syndrome (BS), a rare autosomal recessive salt-losing tubulopathy, classically presents with hyponatremia, hypochloremia, hypokalemic alkalosis, and hyperreninemic hyperaldosteronism. We report a male patient with the atypical presentation
Huijuan Lu +3 more
doaj +1 more source
A novel mutation affecting the arginine-137 residue of AVPR2 in dizygous twins leads to nephrogenic diabetes insipidus and attenuated urine exosome aquaporin-2 [PDF]
Mutations in the vasopressin V2 receptor gene AVPR2 may cause X-linked nephrogenic diabetes insipidus by defective apical insertion of aquaporin-2 in the renal collecting duct principal cell.
Houlberg Hansen, Louise +6 more
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The molecular basis of V2 vasopressin receptor-G Protein coupling selectivity [PDF]
GProteingekoppelte Rezeptoren (GPCRs) stellen eine der größten in der Natur vorkommenden Proteinfamilien dar (Watson and Arkinstall, 1994). GPCRs sind plasmamembranständige Proteine, die mit heterotrimären GProteinen interagieren und eine Vielzahl an ...
Erlenbach, Isolde
core
Diabetes insipidus in pregnancy
Diabetes insipidus is an uncommon condition with various aetiologies. Recent research has uncovered new mechanisms underlying the syndrome. Careful attention to management is essential in pregnant women to avoid serious complications.
Hague, W.
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Nephrogenic diabetes insipidus in a lethargic lithium-treated patient
We report on a patient who developed severe lithium-induced nephrogenic diabetes insipidus (NDI) and neurotoxicity, despite recommended serum lithium levels.
Donders, SHJ, Meinardi, [No Value]
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