Results 11 to 20 of about 23,544 (244)

Gradient washout and secondary nephrogenic diabetes insipidus after brain injury in an infant: a case report

Journal of Medical Case Reports, 2020
Background Disorders of water and sodium balance can occur after brain injury. Prolonged polyuria resulting from central diabetes insipidus and cerebral salt wasting complicated by gradient washout and a type of secondary nephrogenic diabetes insipidus ...
Nathan Chang, Karley Mariano, Lakshmi Ganesan, Holly Cooper, Kevin Kuo   +4 more
doaj   +2 more sources

Lithium treatment, nephrogenic diabetes insipidus and the risk of hypernatraemia: a retrospective cohort study

Therapeutic Advances in Psychopharmacology, 2019
Background: Hypernatraemia is a serious condition that can potentially become life threatening. It is known that lithium is associated with polyuria and nephrogenic diabetes insipidus, risk factors for hypernatraemia.
Michael Ott, Björn Forssén, Ursula Werneke   +2 more
doaj   +2 more sources

Nephrogenic diabetes insipidus

Current Opinion in Pediatrics, 2017
Purpose of review In nephrogenic diabetes insipidus (NDI), the kidney is unable to concentrate urine despite elevated concentrations of the antidiuretic hormone arginine-vasopressin. In congenital NDI, polyuria and polydipsia are present from birth and should be immediately recognized to avoid severe episodes of
Bockenhauer, D, Bichet, DG
openaire   +4 more sources

Hyperactivation of Nrf2 in early tubular development induces nephrogenic diabetes insipidus

Nature Communications, 2017
Nrf2 regulates oxidative and electrophilic stress responses by modulating the expression of enzymes involved in detoxification pathways. Here Suzukiet al.
Takafumi Suzuki, Shiori Seki, Keiichiro Hiramoto, Eriko Naganuma, Eri H. Kobayashi, Ayaka Yamaoka, Liam Baird, Nobuyuki Takahashi, Hiroshi Sato, Masayuki Yamamoto   +9 more
doaj   +2 more sources

AKAPs-PKA disruptors increase AQP2 activity independently of vasopressin in a model of nephrogenic diabetes insipidus

Nature Communications, 2018
Patients suffering from congenital nephrogenic diabetes insipidus (NDI) fail to concentrate urine due to mutations in vasopressin type 2 receptor (V2R). Here Ando et al.
Fumiaki Ando, Shuichi Mori, Naofumi Yui, Tetsuji Morimoto, Naohiro Nomura, Eisei Sohara, Tatemitsu Rai, Sei Sasaki, Yoshiaki Kondo, Hiroyuki Kagechika, Shinichi Uchida   +10 more
doaj   +2 more sources

Characterization of three vasopressin receptor 2 variants: an apparent polymorphism (V266A) and two loss-of-function mutations (R181C and M311V). [PDF]

, 2013
Arginine vasopressin (AVP) is released from the posterior pituitary and controls water homeostasis. AVP binding to vasopressin V2 receptors (V2Rs) located on kidney collecting duct epithelial cells triggers activation of Gs proteins, leading to increased
Armstrong, Stephen P, Ayoub, Mohammed Akli, Feldman, Brian J, Pfleger, Kevin DG, Seeber, Ruth M   +4 more
core   +9 more sources

Hereditary tubulopathies accompanying polyuia

Regulatory Mechanisms in Biosystems, 2021
Tubulopathies are a group of heterogeneous diseases that are manifested in the malfunction of the renal tubules. This review addresses tubulopathies associated with polyuria syndrome, namely renal glucosuria syndrome, nephrogenic diabetes insipidus and ...
M. O. Ryznychuk, V. P. Pishak, N. V. Bacyuk-Ponych, O. V. Pishak   +3 more
doaj   +1 more source

Bioinformatics‐guided disproportionality analysis of sevoflurane‐induced nephrogenic diabetes insipidus using the FDA Adverse Event Reporting System database

British Journal of Clinical Pharmacology, 2023
Sevoflurane is an ether‐based inhalational anaesthetic that induces and maintains general anaesthesia. Our study aimed to detect sevoflurane‐induced nephrogenic diabetes insipidus using data mining algorithms (DMAs) and molecular docking.
Akhil T. Jacob, Ankitha Hari Kumar, Gayethri Halivana, Lipin Lukose, Gouri Nair, Viswam Subeesh   +5 more
semanticscholar   +1 more source

Early onset of nephrogenic diabetes insipidus due to fabry disease in a child with GLA N215S mutation: Case report and literature review

Heliyon, 2023
Background: Fabry disease (FD) is a rare X-linked lysosomal storage disorder. Renal involvement in FD is characterized by proteinuria and progressive renal decline.
Zhihong Lu, Yan Wang, Langping Gao, Li Lin, Lidan Hu, Jianhua Mao   +5 more
doaj   +1 more source

Nephrogenic Diabetes Insipidus following an Off-Label Administration of Sevoflurane for Prolonged Sedation in a COVID-19 Patient and Possible Influence on Aquaporin-2 Renal Expression

Case reports in anesthesiology, 2022
During the recent COVID-19 pandemic, the rapidly progressive shortage of intravenous sedative drugs led numerous intensive care units to look for potential alternatives in patients requiring mechanical ventilation for severe acute respiratory distress ...
C. Dupuis, Arnaud Robert, L. Gérard, J. Morelle, P. Laterre, P. Hantson   +5 more
semanticscholar   +1 more source