Results 101 to 110 of about 20,996 (348)

Do cerebral venous thrombosis risk factors influence the development of an associated venous infarction?

open access: yesNeurología (English Edition), 2011
Introduction: Cerebral venous thrombosis (CVT) is a multifactorial process with a wide clinical spectrum and many associated risk factors (RF) that could be complicated with venous infarction (VI).
I. Sanz Gallego   +3 more
doaj   +1 more source

Screening Routine Clinical Notes for Epilepsy Surgery Candidates Using Large Language Models

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Epilepsy surgery is severely underutilized despite proven efficacy, with substantial under‐referral of eligible patients in routine clinical practice. This study evaluated the potential role of large language models (LLMs) as decision‐support tools for screening unstructured clinical notes to identify epilepsy surgery candidates and ...
Uriel Fennig   +9 more
wiley   +1 more source

Tratamiento previo con estatinas y riesgo de complicaciones infecciosas tras un infarto cerebral agudo

open access: yesNeurología, 2011
Resumen: Introducción y objetivo: Diversos estudios clínicos y experimentales atribuyen un efecto inmunosupresor a las estatinas y la administración de simvastatina en la fase aguda del ictus se ha asociado a mayor frecuencia de infecciones durante el ...
L.A. Rodríguez de Antonio   +6 more
doaj   +1 more source

Incidencia de infección respiratoria asociada a disfagia en pacientes con ictus, tratados en la unidad de ictus del HUCV [PDF]

open access: yes, 2022
Las infecciones respiratorias (IR) son una de las complicaciones más frecuentes tras el ictus. Están asociadas a la presencia de disfagia como consecuencia de la alteración funcional producida por el ictus.
Gómez González, Esther
core  

Unraveling 4‐Phenylbutyrate's Therapeutic Role in SLC6A1 Disorders: Pharmacochaperoning Over HDAC Inhibition

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Variants in SLC6A1, encoding the GABA transporter 1 (GAT‐1), cause epilepsy, autism spectrum disorder, and developmental delay via loss of GABA uptake, impaired trafficking, and ER retention. We previously found that 4‐Phenylbutyrate (PBA), an FDA‐approved drug, restores GABA uptake and reduces seizures in SLC6A1‐related disorders ...
Melissa B. DeLeeuw   +5 more
wiley   +1 more source

Ictus: Prevención terciaria

open access: yes
El ictus es una enfermedad cardiovascular sobre la que se puede realizar una prevención terciaria centrada en reducir las complicaciones de las secuelas generadas por un ictus a través de la incorporación de hábitos de vida saludables entre los que se ...
Blasco-Abadía, Julia   +8 more
core   +1 more source

Factores de riesgo no modificables del ictus [PDF]

open access: yes, 2016
Introducción: Se produce un ictus cuando una región del encéfalo se ve alterada debido a un trastorno de los vasos que van al mismo o que se encuentran en él cuando éstos se obstruyen o rompen.
González Gayo, Carmen
core  

Early Recognition of Treatment‐Responsive Rapidly Progressive Dementia: The Modified STAM3mP Score

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Early identification of patients with treatment‐responsive rapidly progressive dementia (RPD) is important as early treatment improves outcomes. The STAM3P score identifies treatment‐responsive RPD using “high risk” presenting features. We optimized performance by adding a time component (i.e., dementia within 3 months) and validated the ...
R. W. van Steenhoven   +16 more
wiley   +1 more source

Description of stroke mimics after complete neurovascular assessment

open access: yesNeurología (English Edition), 2019
Introduction: A considerable percentage of events initially diagnosed as ischaemic stroke have non-cerebrovascular causes; these are called stroke mimics (SM).
C. Avellaneda-Gómez   +10 more
doaj   +1 more source

A 17 Year Old With Developmental Delay Presenting With Increasing Confusion and Imbalance

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Methylmalonic acidemia is an autosomal recessive genetic disorder primarily caused by defects in methylmalonyl‐CoA mutase and cobalamin (vitamin B12) metabolism. These defects disrupt the tricarboxylic acid cycle and oxidative phosphorylation, leading to the abnormal accumulation of metabolic products such as methylmalonic acid, propionic acid,
Wei Zhao, Yingli Zhang, Hongliang Zheng
wiley   +1 more source

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