Results 181 to 190 of about 546,706 (238)
“The Most Difficult Conversations We Have”: Resident Experiences With Pediatric Neuroprognostication
ABSTRACT Objective Pediatric neuroprognostication is often complicated by uncertainty and embedded in high‐stakes medical decisions. For child neurology residents, participation in neuroprognostication can represent key learning experiences but also comes with emotional and ethical challenges, which poses a risk of moral distress.
Grant L. Lin +7 more
wiley +1 more source
Rewriting SCN1A: Genome Editing for Genetic Epilepsies. [PDF]
Dow SA, Bedrosian TA.
europepmc +1 more source
Abstract Microcytic anemia is among the most common hematological abnormalities in clinical practice and is usually attributable to iron deficiency, thalassemia traits, or anemia of inflammation. A small but clinically important subset of patients, however, has inherited disorders of iron metabolism or heme synthesis presenting with persistent ...
Alexandros Makis +2 more
wiley +1 more source
A Rare EEG Finding of Eye Closure Sensitivity in a Child with Genetic Generalized Epilepsy: A Case Report. [PDF]
Almarwani RAS, Alkalbi AMB, Perez JT.
europepmc +1 more source
ABSTRACT Background and Aims Probiotic supplementation has been proposed as a non‐antibiotic strategy for preventing urinary tract infections (UTIs) in children, but its efficacy remains uncertain. We evaluated the effects of probiotic supplementation on pediatric UTI incidence or recurrence, explored potential dose–response relationships, and assessed
Sayed Yousef Mojtahedi +3 more
wiley +1 more source
The cumulative impact of seizures: the science underlying how seizures beget seizures. [PDF]
Gustin RM, Gholipour T, Peters JM.
europepmc +1 more source
ABSTRACT Background and Aims Doxorubicin‐cyclophosphamide (AC) chemotherapy induces hepatotoxicity through oxidative stress and inflammatory pathway activation, but prospective African data are lacking and conventional liver tests may miss subclinical injury.
Tamrat Nida, Abdisa Tufa Bedada
wiley +1 more source
ATP1A3: Uncommon and wavering epilepsy phenotype in a rare variant. [PDF]
Camussi D +3 more
europepmc +1 more source
ABSTRACT Long‐chain fatty acid oxidation disorders (LC‐FAOD) are rare inherited defects of mitochondrial β‐oxidation that impair energy generation during fasting or metabolic stress. Clinical manifestations range from neonatal hypoketotic hypoglycemia and cardiomyopathy to hepatopathy, recurrent rhabdomyolysis, and chronic myopathy.
Sarah C. Grünert +37 more
wiley +1 more source

