Results 231 to 240 of about 2,159,559 (302)
Large Language Model-Enabled Editing of Patient Audio Interviews From "This Is My Story" Conversations: Comparative Study. [PDF]
Bains B +9 more
europepmc +1 more source
ABSTRACT Objective Accurate localization of epileptogenic tubers (ETs) in patients with tuberous sclerosis complex (TSC) is essential but challenging, as these tubers lack distinct pathological or genetic markers to differentiate them from other cortical tubers.
Tinghong Liu +11 more
wiley +1 more source
El acoso laboral: su peritación Workplace harassment: its expert report
Osvaldo Varela +2 more
doaj
Forensic medical reporting of non-fatal injuries in criminal cases in the Netherlands: a mixed-methods analysis of regional practices. [PDF]
Goudswaard ML +6 more
europepmc +1 more source
Life‐Threatening Bradycardia in Anti‐NMDA‐Receptor Encephalitis and a Novel Use for Permanent Pacing
ABSTRACT Background Pediatric anti‐NMDA receptor encephalitis (pNMDARE) is an autoantibody‐mediated disorder that can cause severe autonomic dysfunction, including symptomatic bradycardia and asystole. Dysautonomia can last for years, making it very challenging to manage.
Sarah Tucker +9 more
wiley +1 more source
ABSTRACT Objective People with epilepsy (PWE) may experience cognitive deficits but fail to undergo formal evaluation. This study compares cognitive status between PWE and healthy controls in the West African Republic of Guinea. Methods A cross‐sectional, case–control study was conducted in sequential recruitment phases (July 2024–July 2025) at Ignace ...
Maya L. Mastick +14 more
wiley +1 more source
Expert Workshop Report 2 which includes the agenda the participants and the outcome of the expert ...
openaire +1 more source
Medical malpractice in pediatric surgery: an analysis of Supreme Court decisions involving physicians. [PDF]
Çördük N, İzci A, Dereli AK, Acar K.
europepmc +1 more source
ABSTRACT Objective Super‐Refractory Status Epilepticus (SRSE) is a rare, life‐threatening neurological emergency with unclear etiology in many cases. Mitochondrial dysfunction, often due to disease‐causing genetic variants, is increasingly recognized as a cause, with each gene producing distinct pathophysiological mechanisms.
Pouria Mohammadi +2 more
wiley +1 more source

