Results 141 to 150 of about 71,933 (306)

The Impact of Aquaporin‐4 Deletion on K+‐Induced Astrocytic Swelling Depends on K+ Concentration

Glia, Volume 74, Issue 1, January 2026.
Swelling due to 10 mM [K+]o is reduced in astrocytes devoid of aquaporin‐4, while there is no difference between genotypes when exposed to 50 mM [K+]o. The two [K+]o concentrations induce distinct astrocytic Ca2+ signaling in the two genotypes pointing to a possible mechanistic basis of the differences observed. ABSTRACT Astrocytes swell in response to
Cecilie Bugge Bakketun, Lena Catherine Roth, Daniel Marelius Bjørnstad, Ole Petter Ottersen, Vidar Jensen, Rune Enger   +5 more
wiley   +1 more source

Evaluating Hyponatremia [PDF]

JAMA, 2015
David M, Cohen, David H, Ellison
openaire   +2 more sources

Severe asymptomatic maternal antepartum hyponatremia leading to neonatal seizures: prevention is better than cure

, 2015
Enrico Valerio, Margherita Fantinato, Irene Giovannini, Eugenio Baraldi, Lino Chiandetti   +4 more
openalex   +1 more source

The Faculty Notebook, September 2002

, 2002
The Faculty Notebook is published periodically by the Office of the Provost at Gettysburg College to bring to the attention of the campus community accomplishments and activities of academic interest.
Provost\u27s Office,
core  

A Novel PCK1 Gene Variant Associated With Cytosolic Phosphoenolpyruvate Carboxykinase Deficiency: Two Siblings With Different Clinical Presentations

JIMD Reports, Volume 67, Issue 1, January 2026.
ABSTRACT Cytosolic phosphoenolpyruvate carboxykinase (PEPCK‐C) deficiency is a rare autosomal recessive gluconeogenesis disorder caused by variants in the PCK1 gene. Clinically, PEPCK‐C deficiency is characterized by recurrent episodes of fasting‐induced hypoglycemia, liver dysfunction, and seizures, with the first hypoglycemic episode typically ...
Lauma Vasiļevska, Ieva Puķīte, Madara Auzenbaha, Dmitrijs Rots, Ieva Grīnfelde, Andžela Lazdāne, Sebastian Schulz‐Jürgensen   +6 more
wiley   +1 more source

Case Report: Compound Heterozygous SCNN1B Mutations Causing Pseudohypoaldosteronism Type 1B2 in Neonatal Twins

Molecular Genetics &Genomic Medicine, Volume 14, Issue 1, January 2026.
First Chinese neonatal cases of systemic PHA1B from novel compound‐heterozygous SCNN1B variants (c.585+2T>C; c.1544T>C) presented with life‐threatening hyperkalemia and hyponatremia unresponsive to steroids. Early genetic testing enabled targeted sodium supplementation and potassium‐binding therapy, normalizing electrolytes and underscoring SCNN1B ...
Zhiping Wang, Lijuan Long, Hongjuan Bi
wiley   +1 more source

Manual dilution of CRRT fluids in anuric patients with severe hyponatremia: a case report and systematic review [PDF]

Mark V. Koning, Lassima Reijnen, Frits A.W. Kemperman, Eugenie Schipper-Reintjes   +3 more
openalex   +1 more source

Severe hyponatremia after donor nephrectomy

, 2020
IhabA Ibrahim, EhabA Hassan, TariqZ Ali, JensG Brockmann, HassanA Aleid   +4 more
openalex   +1 more source

Exercise associated hyponatremia (EAH) [PDF]

, 2009
This issue of eMedRef provides information to clinicians on the pathophysiology, diagnosis, and therapeutics of exercise associated ...
Mahmoodi, Maria, Scuderi, Christopher
core  

Hyponatremia and hyperkalemia associated with idiopathic or experimentally induced chylothorax in four dogs [PDF]

, 1991
Μ. D. Willard, Theresa W. Fossum, Andrew Torrance, Aunna C. Lippert   +3 more
openalex   +1 more source