Results 41 to 50 of about 1,221,013 (139)
Urine electrolytes guide treatment of Gitelman syndrome and recurrent syncope—A case report
Physiological Reports, Volume 14, Issue 18, September 2026.Abstract Syncope is a common reason for inpatient admission. Few case studies describe an association between syncope and Gitelman syndrome (GS). Herein, we present a case of a woman with hypokalemia and recurrent syncope which eventually led to a diagnosis of GS. A physiologic approach to urine electrolyte interpretation informed clinical decisions to
Saloni Agrawal +3 more
wiley +1 more source
Reduced-complexity syndrome-based TTCM decoding [PDF]
, 2013 The iterative decoder of Turbo Trellis Coded Modulation (TTCM) exchanges extrinsic information between the constituent TCM decoders, which imposes a high computational complexity at the receiver. Therefore we conceive the syndrome-based block decoding of
Ng, Soon Xin +2 more
core +1 more source
Alzheimer's &Dementia, Volume 22, Issue 8, August 2026.Abstract Mild cognitive impairment and dementia are underrecognized in primary care, contributing to delayed diagnosis and limited access to care. Growing research has focused on improving cognitive evaluation in primary care, including the development of digital cognitive assessments (DCAs), which are emerging as scalable tools to expand access to ...
Pierre N. Tariot +6 more
wiley +1 more source
Etiological and Metabolic Profile Hypokalemic Periodic Paralysis [PDF]
, 2008 CONCLUSION: 1. Among the patients with Hypokalemic Periodic Paralysis two thirds of them are due to secondary causes. 2. In our study the common causes are Idiopathic or sporadic periodic paralysis, Gitelman’s/Bartter syndrome and Distal Renal Tubular
Nivas, B
core
Home Parenteral Support in Severe Gitelman Syndrome: A Case Report
Clinical Case Reports, Volume 14, Issue 7, July 2026.ABSTRACT Gitelman syndrome (GS), also known as familial hypokalaemia‐hypomagnesemia, is a rare autosomal recessive renal tubular disorder characterized by hypokalaemia, hypomagnesemia, metabolic alkalosis, and hypocalciuria. Electrolyte replacement of potassium and magnesium remains the mainstay of management, with oral supplementation achieving this ...
Georgia Martin +2 more
wiley +1 more source
Molecular Genetics &Genomic Medicine, Volume 14, Issue 7, July 2026.We report pseudo‐dominant PCD inheritance in a Chinese family due to novel DNAAF1 mutations. Affected members across two generations showed significant variability in lung disease progression and visceral arrangement. ABSTRACT Background Primary ciliary dyskinesia (PCD) is a rare, genetically heterogeneous disorder typically inherited in an autosomal ...
Zhuoyao Guo +3 more
wiley +1 more source
Bilateral Idiopathic Sclerochoroidal Calcifications
, 2017 Background: Sclerochoroidal calcification (SCC) is a rare and benign condition found mostly in middle-aged and elderly Caucasian men, characterized by multiple yellow-white lesions seen most commonly in the ...
Nauman A. Chaudhry +3 more
core +1 more source
Cowden syndrome - Diagnostic skin signs [PDF]
, 2001 Cowden syndrome is a rare autosomal dominant familial cancer syndrome with a high risk of breast cancer. The most important clinical features include carcinomas of the breast and thyroid, and hamartomatous polyps of the gastrointestinal tract.
Burgdorf, Walter H. C. +5 more
core +1 more source
Veterinary Clinical Pathology, Volume 55, Issue 2, Page 172-177, June 2026.Abstract Urinary extracellular vesicles (UEVs) are membranous particles that carry renal tubular transporter proteins. Here, we evaluate whether selected renal tubular transporter proteins can be detected in UEVs isolated from small volume (1–5 mL) canine urine samples of healthy dogs and canine patients with elevated circulating parathyroid hormone ...
L. J. McGravey +2 more
wiley +1 more source
Variability in fricative production of young people with Down's syndrome : an EPG analysis [PDF]
, 2007 Speech production in Down's syndrome is highly variable, with particular problems arising from complex articulations such as fricatives. In this paper, EPG analysis is used to study the variation in the production of the fricatives /s/ and /sh/ in 6 ...
Hardcastle, William +4 more
core +3 more sources