Results 151 to 160 of about 71,933 (306)
Hyponatremia in babies: a 11-year single-center study
IntroductionHyponatremia is one of the most prevalent water-electrolyte disturbances encountered in clinical practice in pediatrics and can arise from various conditions. However, there are limited reports on hyponatremia in hospitalized infants.
Xu Liu +4 more
doaj +1 more source
This graphical abstract shows GFAP‐IgG detection using tissue‐based and cell‐based assays (top). It illustrates the selection of patients for comparing favorable and unfavorable prognosis groups (bottom left). Finally, it presents multiple regression analysis results identifying predictors of poor prognosis 6 months after admission (bottom right ...
Akio Kimura +7 more
wiley +1 more source
Effect of experimental hypoosmolar hyponatremia on the blood brain barrier and brain edema formation
The most frequent cause of hyponatremia is water retention due to the increase in blood levels of antidiuretic hormone (vasopressin, AVP). Hyponatremia is associated with neurological deficits, which are mainly linked to brain edema.
Marta Aleksandrowicz +4 more
doaj +1 more source
Severe Abdominal Pain with Hyponatremia [PDF]
Van Leung‐Pineda, Don P. Wilson
openalex +1 more source
The Faculty Notebook, February 2008
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 +1 more source
Central and extrapontine myelinolysis following correction of extreme hyponatremia. Case report and review of the literature [PDF]
Neðst á síðunni er hægt að nálgast greinina í heild sinni með því að smella á hlekkinn View/OpenWe report a case of a 43-year-old woman who developed osmotic demyelination syndrome following correction of extreme hyponatremia that was considered to be of
Runólfur Pálsson, +1 more
core
February 2026 global research highlights
Hong Kong Journal of Emergency Medicine, Volume 33, Issue 1, February 2026.
wiley +1 more source
Abstract Background Dysfunction of δ‐aminolevulinic acid dehydratase (ALAD), the second enzyme involved in heme biosynthesis, leads to two pathologies: genetic and acquired. The genetic form is an ultrarare, severe childhood‐onset disease inherited in an autosomal recessive manner, whereas the acquired form usually affects adults due to enzyme ...
Elena Di Pierro +22 more
wiley +1 more source

