Results 111 to 120 of about 23,590 (248)
Sevoflurane and nephrogenic diabetes insipidus on the rise: copeptin to the rescue?
Critical Care, 2019 With interest, we read the recent paper by Nigro et al. on the differential diagnosis of hypernatremia in intensive care unit (ICU) [1]. One of their main findings was an evidently higher copeptin levels in nephrogenic diabetes insipidus (NDI), compared ...
P. Honore +5 more
semanticscholar +1 more source
Ожирение и метаболизмNephrogenic diabetes insipidus is a heterogeneous disease in the etiopathogenesis of which are involved acquired and congenital factors. In this case, the kidneys do not respond to vasopressin and continue to produce large concentrated volumes of urine ...
R. M. Guseinova +2 more
doaj +1 more source
Development of Genetically Engineered Mice Lacking All Three Nitric Oxide Synthases
Journal 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
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Claudins in the Renal Collecting Duct [PDF]
, 2019 The renal collecting duct fine-tunes urinary composition, and thereby, coordinates key physiological processes, such as volume/blood pressure regulation, electrolyte-free water reabsorption, and acid-base homeostasis.
Leiz, Janna, Schmitt-Ott, Kai M.
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Clinical and Experimental Nephrology, 2018 Congenital nephrogenic diabetes insipidus (NDI) is characterized by defective urine concentrating ability. Symptomatic polyuria is present from birth, even with normal release of the antidiuretic hormone vasopressin by the pituitary.
Fumiaki Ando, S. Uchida
semanticscholar +1 more source
Partial nephrogenic diabetes insipidus associated with Castleman’s disease
BMC 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
Genetic basis of nephrogenic diabetes insipidus
Molecular and Cellular Endocrinology, 2022 Marguerite Hureaux, R. Vargas-Poussou
semanticscholar +1 more source
Partial nephrogenic diabetes insipidus associated with lithium therapy
BMJ Case Reports, 2019 A 40-year-old Caucasian man developed excessive thirst and polyuria particularly at night over the preceding 6 months. He had been taking lithium for 16 years for the treatment of bipolar affective disorder.
Eka Nandoshvili, S. Hyer, Nikhil Johri
semanticscholar +1 more source
X-Linked Recessive Form of Nephrogenic Diabetes Insipidus in A 7-Year-Old Boy
Balkan 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
Diabetes insípida central en un perro [PDF]
, 1999 Se describe un caso de diabetes insípida central [DIC] en un perro. Este caso es particularmente interesante pues se observan modificaciones electrolíticas poco habituales.
Cano Rábano, María José +4 more
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