Results 31 to 40 of about 11,822 (153)

Federal clinical guidelines on diagnosis and treatment of diabetes insipidus in adults

Ожирение и метаболизм, 2018
We do not recommend population screening for diabetes insipidus (DI) (B3). We recommend to perform diagnostic testing for central diabetes insipidus (CDI) in patients who underwent neurosurgery, after skull and brain trauma, subarchnoid hemorrhage (B3 ...
Ivan I. Dedov, Galina A. Mel'nichenko, Ekaterina A. Pigarova, Larisa K. Dzeranova, Liudmila Y. Rozhinskaya, Elena G. Przhiyalkovskaya, Zhanna E. Belaya, Andrey Y. Grigoriev, Alexander V. Vorontsov, Alexander S. Lutsenko, Ludmila I. Astafyeva   +10 more
doaj   +1 more source

POSTOPERATIVE RISE IN SERUM SODIUM LEVEL, INDICATOR OF DIABETES INSIPIDUS AFTER PITUITARY ADENOMA SURGERY

Pakistan Armed Forces Medical Journal, 2019
Objective: To study the efficacy of post operative rise in serum sodium level as indicator of diabetes insipidus after pituitary adenoma surgery.
Noor-ul-Huda Maria, Qurrat-Ul-Ain ., Muhammed Anwar   +2 more
doaj   +4 more sources

Juvenile-onset gout and adipsic diabetes insipidus: A case report and literature review

Journal of International Medical Research, 2018
The prevalence of juvenile-onset gout has been increasing. Hereditary factors and secondary diseases should be considered in these patients. Adipsic diabetes insipidus (ADI) is characterized by arginine vasopressin (AVP) deficiency, which results in ...
Yun Zhang, Dongmei Wang, Yiding Feng, Wen Zhang, Xuejun Zeng   +4 more
doaj   +1 more source

Lower Urinary Tract Symptoms as Diagnostic Clues in Parkinsonism: A Practical Framework for Neurologists

Movement Disorders Clinical Practice, EarlyView.
Abstract Background Lower urinary tract symptoms (LUTS) are among the most prevalent nonmotor complaints across the parkinsonian spectrum, yet they remain underutilized as diagnostic and management signals in neurology practice. Although prior reviews have characterized disease‐specific patterns of urinary dysfunction, and recent guidelines address ...
Saar Anis, Omer Anis, Abhishek Lenka, Junaid H. Siddiqui   +3 more
wiley   +1 more source

Hypotonic-mediated [Ca²⁺]_i signals require Ca²⁺ influx via TRPC3 in CD cells.

, 2019
(A) The average time course of [Ca2+]i changes in response to 10X elevations in perfusion rate from 1.5 ml/min to 15 ml/min (high flow) and application of hypotonic medium (220 mOsm) in the absence and in the presence of a TRPV4 inhibitor, ruthenium red (
Sean P. Marrelli (8150100), Oleg Zaika (53586), Viktor N. Tomilin (8150094), Mykola Mamenko (346760), Guohui Ren (8150097), Oleh Pochynyuk (346764), Lutz Birnbaumer (281971)   +6 more
core   +1 more source

Hypotonic Shock Induced Ascorbate Release [PDF]

, 2004
Ascorbate (Asc) is a key antioxidant in preventing cardiovascular dysfunction during diseases exacerbated by altered shear stress. According to the literature endothelial responses to hypotonic shock share some characteristics with those induced by shear
Gill, Rupinder
core   +1 more source

Broadening horizons: Pathogenesis and therapeutics of renal ciliopathies

Journal of Cell Communication and Signaling, Volume 20, Issue 3, September 2026.
This review elucidates the molecular mechanisms and aberrant signaling pathways in renal ciliopathies, links genetic heterogeneity to clinical phenotypes, and lays a theoretical basis for prenatal diagnosis and novel therapies. Abstract Renal ciliopathies encompass a spectrum of genetic disorders arising from structural or functional impairments of ...
Qiaowei Zhang, Shuwen Xue, Zhi Gao, Panlai Shi, Li Wang, Qi Feng, Xiangdong Kong, Xiaofan Zhu   +7 more
wiley   +1 more source

An Optimized Diagnostic Approach for Adults With Suspected Inherited Metabolic Disorders

Journal of Inherited Metabolic Disease, Volume 49, Issue 5, September 2026.
A multidisciplinary strategy that integrates deep phenotyping with expert genetic interpretation substantially increases the likelihood of reaching a diagnosis in adults suspected of having an IMD. ABSTRACT Inherited metabolic disorders (IMDs) arise from defects in metabolic pathways essential for normal biochemical function.
Machteld M. Oud, Elise A. Ferreira, Clara D. M. van Karnebeek, Robin Wijngaard, Nicole I. Wolf, Marc Engelen, Mareen Datema, Sacha Ferdinandusse, André B. P. van Kuilenburg, Laura Steinbusch, Saskia N. van der Crabben, Mirjam Langeveld, on behalf of the ZOEMBA Study Group   +12 more
wiley   +1 more source

Urinary Dysfunction in Myasthenic Syndromes: A Scoping Review of Clinical Features and Treatment‐Related Associations

Muscle &Nerve, Volume 74, Issue S1, Page S97-S107, September 2026.
ABSTRACT Urinary dysfunction has been reported in association with myasthenic syndromes, including myasthenia gravis (MG), Lambert–Eaton myasthenic syndrome (LEMS), and congenital myasthenic syndromes (CMS), but evidence regarding its prevalence, clinical impact, pathophysiology, and management remains limited.
Julia M. Augustin, Lillith Horstkorte, Hellen Schmidt, Blanca G. Sánchez Navarro, Avan Kader, Inga Koneczny, Holly M. Nelson, Pratishtha P. Wadnerkar, Rafael Meleka Hanna, Ayşe N. Özdağ Acarlı, Piraye Oflazer, Atay Vural, Franz Blaes, Miriam L. Fichtner   +13 more
wiley   +1 more source

Severe Hypernatraemia Secondary to Adipsia Associated With a Pituitary Macroadenoma in a Dog: A Case Report

Veterinary Medicine and Science, Volume 12, Issue 5, September 2026.
Severe hypernatraemia (Na+ 192 mmol/L) secondary to adipsia was successfully managed through gradual sodium correction, close monitoring and assisted water supplementation in a dog with a pituitary macroadenoma. No neurologic complications occurred during correction, and serum sodium concentrations remained stable for 9 months. This case highlights the
Gyo‐Bin Choo, Bum‐kyu Choi, Sooyoung Choi, Daji Noh, Ju‐Hyun An   +4 more
wiley   +1 more source