Results 61 to 70 of about 2,038 (265)

Posterior Cortical Atrophy in the Asia‐Pacific: A Report From the PCA Asian Workgroup

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Posterior Cortical Atrophy (PCA) is a distinct dementia syndrome primarily affecting spatial abilities and visual processing. It is associated with degeneration in the posterior part of the brain. PCA is subclassified into PCA‐pure and PCA‐plus syndromes based on consensus criteria.
Yuttachai Likitjaroen   +11 more
wiley   +1 more source

Onasemnogene Abeparvovec in Type I Spinal Muscular Atrophy: 24‐Month Follow‐Up From the Italian Registry

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Onasemnogene abeparvovec (OA) is an AAV9‐based gene therapy for spinal muscular atrophy type I (SMA I). Real‐world outcomes show increased response variability compared to clinical trials, and follow‐up data beyond 12–18 months are limited.
Marika Pane   +43 more
wiley   +1 more source

Music detection from broadcast contents using convolutional neural networks with a Mel-scale kernel

open access: yesEURASIP Journal on Audio, Speech, and Music Processing, 2019
We propose a new method for music detection from broadcasting contents using the convolutional neural networks with a Mel-scale kernel. In this detection task, music segments should be annotated from the broadcast data, where music, speech, and noise are
Byeong-Yong Jang   +3 more
doaj   +1 more source

Reperfusion‐Dependent Outcomes After Endovascular Thrombectomy Stratified by NIHSS‐ASPECTS Clinical‐Core Mismatch

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective This analysis evaluates the effect of successful reperfusion on functional outcomes after MT, stratified by admission National Institutes of Health Stroke Scale (NIHSS) and Alberta Stroke Program Early CT Score (ASPECTS) as surrogates for clinical‐core mismatch, using multicenter registry data.
Felix Schlicht   +53 more
wiley   +1 more source

Cracking the Code: Genotype–Phenotype Correlation Models in Sarcoglycanopathies

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Sarcoglycanopathies are among the most severe limb‐girdle muscular dystrophies (LGMD), though milder presentations have been described. These diseases are primarily caused by missense variants, but the limited predictability of their effect on protein maturation, complex formation, and transport has hindered reliable genotype ...
Leonela Luce   +72 more
wiley   +1 more source

Al-Husseini Literature: An Approach to the Foundation Project

open access: yesدواة
    This research attempts to develop a foundational approach to Husayni literature, rooting its epistemological foundations in their various historical, documentary, and critical orientations.
Asst. Prof. Hussam Qaddoori Abd   +1 more
doaj   +1 more source

Multiple Sclerosis Relapse Activity After Ozanimod Discontinuation in DAYBREAK Trial Participants

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
Multiple Sclerosis Relapse Activity After Ozanimod Discontinuation in DAYBREAK Trial Participants. ABSTRACT Objective Return of disease activity is expected when patients discontinue disease‐modifying therapy (DMT) for multiple sclerosis (MS). Some MS DMTs are associated with higher‐than‐expected disease activity (rebound) after discontinuation.
Ralf Gold   +12 more
wiley   +1 more source

Representational Collisions in Quest of a Character: Maria Lacerda de Moura in the Traffic of Lights and Sounds

open access: yesRevista Estudos Feministas, 2009
From the documentary Maria Lacerda de Moura: trajetória de uma rebelde, the present article analyzes the delicate exercise of re-creating the biography of historical personalities in a film, where the conjunction of different points of view, filmmaking
Ana Amélia Brasileiro Medeiros Silva
doaj  

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

Educational and Lingusitic Problems of the Idigenous Peoples of Venezuela

open access: yesIkala: Revista de Lenguaje y Cultura, 2009
  In this paper, we examine the situation of Venezuelan indigenous peoples and their respective languages. We present the history and scope of the System of Intercultural Bilingual Education and discuss the implications of language policies of ...
Natalia Bondarenko Pisemskaya
doaj  

Home - About - Disclaimer - Privacy