Results 251 to 260 of about 2,115,183 (392)

Late Pregnancy Antiseizure Medication Exposure and Offspring Neurodevelopmental Risk: A Multi‐Child Cohort Study

open access: yesAnnals of Neurology, EarlyView.
Objective Antiseizure medication (ASM) use during pregnancy has increased over the past decade. However, evidence linking prenatal ASM exposure to neurodevelopmental disorders (NDDs) in offspring remains inconsistent. This study evaluated whether prenatal ASM exposure increases the risk of NDDs in children.
Odile Sheehy   +13 more
wiley   +1 more source

Early detection of abnormalities in partial epilepsy using magnetic resonance. [PDF]

open access: bronze, 1993
J. Helen Cross   +7 more
openalex   +1 more source

SYN1 loss-of-function mutations in autism and partial epilepsy cause impaired synaptic function.

open access: yesHuman Molecular Genetics, 2011
A. Fassio   +20 more
semanticscholar   +1 more source

Real‐World Effectiveness of Switching to Oral or Infusion Versus Injectable Disease‐Modifying Therapy in Pediatric Multiple Sclerosis

open access: yesAnnals of Neurology, EarlyView.
Objective To assess real‐world effectiveness of switching disease‐modifying therapy (DMT) in pediatric multiple sclerosis (MS) and clinically isolated syndrome (CIS) initially treated with platform injectables on disease activity. Methods Of 2615 pediatric‐onset demyelinating disease patients at 12 clinics in the United States (US) Network of Pediatric
Aaron W. Abrams   +27 more
wiley   +1 more source

Autosomal Dominant Partial Epilepsy with Auditory Features: Description of a New Family [PDF]

open access: bronze, 2000
Roberto Michelucci   +5 more
openalex   +1 more source

Clinical comparability of the new antiepileptic drugs in refractory partial epilepsy: A systematic review and meta‐analysis

open access: yesEpilepsia, 2011
João Costa   +5 more
semanticscholar   +1 more source

Anatomical Progression of Neuropathology in FTLD‐TDP Type C and Linkage to Annexin A11

open access: yesAnnals of Neurology, EarlyView.
Objective Frontotemporal lobar degenerations (FTLD)‐TDP type C (TDP‐C) is distinguished from other FTLD‐TDP subtypes by 3 unique features: (1) invariable onset in the anterior temporal lobe (ATL), (2) phosphorylated TDP‐43 (pTDP) neurites in cortex, and (3) colocalization of all pTDP deposits with annexin A11 (ANXA11).
Allegra Kawles   +7 more
wiley   +1 more source

Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features

open access: yesNature Genetics, 2002
S. Kalachikov   +17 more
semanticscholar   +1 more source

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