Results 131 to 140 of about 574,481 (313)

Epilepsy‐Associated Variants of a Single SCN1A Codon Exhibit Divergent Functional Properties

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Pathogenic variants in SCN1A, which encodes the voltage‐gated sodium channel NaV1.1, are associated with multiple epilepsy syndromes exhibiting a range of clinical severity. SCN1A variants are reported in different syndromes, including Dravet syndrome, which is associated with loss‐of‐function, whereas neonatal/infantile‐onset ...
Lanie N. Liebovitz   +3 more
wiley   +1 more source

Text as Tradition – Tradition as Text

open access: yesSvensk Teologisk Kvartalskrift, 2023
From its inception, early Christianity exhibited a kind of textuality that differs in striking ways from modern, academic textuality. While the various skills comprising literacy (reading, writing, and so on) were rare and unevenly distributed in the early Roman imperial period, nevertheless the early Christians and other Jews lived in a world crowded ...
openaire   +1 more source

Elevated Connectivity During Language Processing Is Associated With Cognitive Performance in SeLECTS

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Self‐Limited Epilepsy with Centrotemporal Spikes (SeLECTS) is associated with language impairments despite seizures originating in the motor cortex, suggesting aberrant cross‐network interactions. Here we tested whether functional connectivity in SeLECTS during language tasks predicts language performance.
Wendy Qi   +8 more
wiley   +1 more source

Culture and Tradition; Culture et tradition

open access: yes, 1996
The politics of culture and public sector folklore in Québec: the role of CÉLAT and I'ethnologie Quebecois / Anna Kearney Guigné -- Power concealed-power revealed: towards new meanings of menstruation / Lisa J.

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Relationship Between Neurologic Symptoms and Signs and FMR1 Genotype in Premutation Carriers

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background and Objectives Fragile X‐associated Tremor/Ataxia Syndrome (FXTAS) is the most severe late‐onset condition caused by a premutation in the FMR1 gene, characterized by expanded CGG triplet repeats of 55–200. Clinical presentations of FXTAS, including gait ataxia, kinetic tremor, cognitive decline, and rare Parkinsonism, are linked to ...
Flora Tassone   +8 more
wiley   +1 more source

Culture and Tradition; Culture et tradition

open access: yes, 1993
Éditorial (Université Laval) / Marie-France Saint-Laurent -- Les Québécois à Old Orchard / Marie-Hélène Tremblay -- L'auberge de jeunesse: lieu d'hébergement ou de rencontre?

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Tradition och bildning mellan reaktion och revolution

open access: yes, 2020
I den här texten utlägger jag betydelsen av tradition och bildning, reflekterar över sambandet mellan dem och landar till sist i frågan om dessa begrepp med nödvändighet har konservativa implikationer, en fråga som jag besvarar ...
Sigurdson, Ola,
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Effectiveness of rTMS on Working Memory and Inhibitory Impairments in Patients With Post‐Stroke Executive Deficits

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Considerable efforts have been dedicated to developing effective treatments for post‐stroke executive impairment (PSEI), among which repetitive transcranial magnetic stimulation (rTMS) has shown great potential. This study aimed to investigate the therapeutic effects of high‐frequency rTMS on working memory (WM) and response ...
Mengting Lao   +6 more
wiley   +1 more source

Culture and Tradition; Culture et tradition

open access: yes, 1980
Vers une deontologie du folklorist / Colette Dufresne, Jehan Etcheverry , Vivian Labrie, Rose Bilodeau Lahaie, Richard Luneau – The child ballads as found in Newfoundland: a survey / Colin Quigley -- Effets reciproques entre contour et assistance dans ...

core  

Prognostic Value of Neurofilament Light Chain and Glial Fibrillary Acidic Protein in ALD‐Related Myelopathy

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background X‐linked adrenoleukodystrophy (X‐ALD) is a neurometabolic disorder caused by pathogenic variants in ABCD1, leading to slowly progressive spinal cord disease in nearly all affected men. Sensitive biomarkers to quantify disease severity and predict progression are needed for clinical care and trial design.
Eda G. Kabak   +4 more
wiley   +1 more source

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