Results 81 to 90 of about 1,031,173 (193)

Development of Genetically Engineered Mice Lacking All Three Nitric Oxide Synthases

open access: yesJournal of Pharmacological Sciences, 2006
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
doaj   +1 more source

Efficacy of COX-2 inhibitors in a case of congenital nephrogenic diabetes insipidus. [PDF]

open access: yes, 2005
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
core   +1 more source

X-Linked Recessive Form of Nephrogenic Diabetes Insipidus in A 7-Year-Old Boy

open access: yesBalkan Journal of Medical Genetics, 2014
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
doaj   +1 more source

Partial nephrogenic diabetes insipidus associated with Castleman’s disease

open access: yesBMC Nephrology, 2019
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 difficulties in infancy as an early symptom of different forms of diabetes insipidus – a series of cases

open access: yesPediatria Polska
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
doaj   +1 more source

Type 1 Bartter syndrome presenting as primary diabetes insipidus: a rare Case Report with 8-year follow-up

open access: yesFrontiers in Genetics
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]

open access: yes, 2016
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
core   +1 more source

The molecular basis of V2 vasopressin receptor-G Protein coupling selectivity [PDF]

open access: yes, 2003
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

open access: yes, 2009
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.
core   +1 more source

Nephrogenic diabetes insipidus in a lethargic lithium-treated patient

open access: yes, 1997
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]
core   +1 more source

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