Results 141 to 150 of about 21,961 (301)

Reality Winners

open access: yes
Critical Quarterly, EarlyView.
Lee Grieveson
wiley   +1 more source

Patterns of phosphorylated tau accumulation in a spectrum of acquired and developmental brain lesions associated with refractory epilepsy

open access: yesEpilepsia, EarlyView.
Abstract Objective Phosphorylated tau (pTau) has been reported in surgical resections in refractory epilepsy. It is unclear whether this is activity‐driven physiological pTau or signifies the advent of neurodegenerative cascades, relevant to memory decline.
Alicja Mrzyglod   +13 more
wiley   +1 more source

Assosiation study between IL1RA gene polymorphism with febrile convulsion in Shahrekord children [PDF]

open access: yes, 2010
زمینه و هدف: امروزه تب و تشنج بخش قابل ملاحظه ای از موارد بستری کودکان را در بیمارستان ها به خود اختصاص داده است. با توجه به تحقیقات اخیر که نوعی ارتباط مثبت بین وجود سابقه خانوادگی برای تشنج (از نظر نوع و سن بروز بیماری در کودک) و ابتلا به این بیماری را
Ahadi, AliMohammad.   +7 more
core  

Predictors of atypical language lateralization in focal epilepsy: A mega‐analysis of fMRI evidence

open access: yesEpilepsia, EarlyView.
Abstract Objective To identify predictors of language lateralization derived from functional magnetic resonance imaging (fMRI) in children and adults with left‐ and right‐sided focal epilepsy. Methods We conducted a mega‐analysis of data from 914 individuals from 24 samples. We used multilevel models to identify predictors of language lateralization in
Freya Prentice   +8 more
wiley   +1 more source

Prolonged febrile seizures in the immature rat model enhance hippocampal excitability long term. [PDF]

open access: yes, 2000
Febrile seizures (FSs) constitute the most prevalent seizure type during childhood. Whether prolonged FSs alter limbic excitability, leading to spontaneous seizures (temporal lobe epilepsy) during adulthood, has been controversial.
Baram, TZ   +5 more
core  

SCN9A should not be considered an epilepsy gene; Refuting a gene–disease association

open access: yesEpilepsia, EarlyView.
Abstract Objective The SCN9A gene is primarily expressed in nociceptive pathways within the peripheral nervous system, and pathogenic variants are associated with human pain disorders. In recent years, several studies have proposed SCN9A as a monogenic cause of epilepsy.
Ismael Ghanty   +7 more
wiley   +1 more source

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