Results 131 to 140 of about 43,777 (261)
Sex Representation in US Stroke Clinical Trials: A Decade of Trends and Challenges
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Stroke remains a major cause of disability and mortality in the US, with significant sex‐based disparities, and females remain underrepresented in stroke clinical trials. We aimed to examine sex representation in US‐based stroke clinical trials, identify trial characteristics associated with higher female enrollment (≥ 50%), and ...
Chaitali Dagli +5 more
wiley +1 more source
Acerca del género Synammia Presl (Polypodiceae S. STR.)
Revista del Museo de La PlataEl género Synammia fue creado por Presl en 1836. Después pasó al olvido o se lo consideró un sinónimo de los géneros de los cuales había sido segregado (Polypodium L., Goniophlebium (Blume) Presl).En 1947, Copeland revalida y discute la posición y ...
Elías Ramón De la Sota
doaj
Cracking the Code: Genotype–Phenotype Correlation Models in Sarcoglycanopathies
Annals 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
Perspectivas de las Ciencias Económicas y Jurídicas, 2017 Uno de los fenómenos políticos más significativos que se presentó en las últimas dos décadas en América del Sur fue la aparición de los llamados gobiernos progresistas en países como Ecuador, Venezuela y Bolivia.
Octavio Humberto Moreno Velador +1 more
doaj
Multiple Sclerosis Relapse Activity After Ozanimod Discontinuation in DAYBREAK Trial Participants
Annals 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
LA POLÍTICA DE ACCESO DE UNA INSTITUCIÓN UNIVERSITARIA DE RECIENTE CREACIÓN: EL CASO DEL INSTITUTO UNIVERSITARIO DEL GRAN ROSARIO [PDF]
, 2009 El propósito del trabajo radica en relatar la política de acceso desarrollada durante los años 2008 y 2009 por una institución universitaria de reciente creación: el caso del Instituto Universitario del Gran Rosario –IUGR-.
DIODATI, MARIANO, MARTINEZ, CARLOS
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Relationship Between Neurologic Symptoms and Signs and FMR1 Genotype in Premutation Carriers
Annals 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
, 2020 Incluye bibliografía.En esta publicación se recogen los trabajos seleccionados en la convocatoria realizada con anterioridad al seminario, así como las ponencias de expertos especialmente invitados, que enriquecieron la discusión en las diferentes mesas ...
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Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective To (1) validate GAD65‐ELISA detection and quantification for type 1 diabetes mellitus and autoimmune neurological diagnoses, (2) correlate ELISA results (reference range < 5 IU/mL) with established radioimmunoprecipitation assay (RIA; ≤ 0.02 nmol/L), and (3) define ELISA clinical utility and pitfalls.
Andrew McKeon +11 more
wiley +1 more source
RNA Sequencing Resolves Cryptic Pathogenic Variants in Mitochondrial Disease
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Mitochondrial diseases are the most common inherited metabolic disorders, characterized by pronounced clinical and genetic heterogeneity that complicates molecular diagnosis. Although DNA‐based sequencing approaches have become standard in genetic testing, up to half of patients remain without a definitive diagnosis.
Zhimei Liu +21 more
wiley +1 more source