Results 41 to 50 of about 1,340,927 (354)
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Mutations in myelin regulatory factor (MYRF) are linked to demyelinating disorders. We report a 38‐year‐old male who developed acute symmetric leukoencephalopathy mimicking a stroke following an influenza A virus infection. While clinical symptoms markedly improved with corticosteroids, MRI revealed persistent white matter lesions, contrasting
Jinghan Hu +5 more
wiley +1 more source
Design and evaluation of the effectiveness of a sport-based intervention to teduce impulsive symptoms in an adoslescents with severe mental disorder admitted to the Child and Adolescent Day Hospital of Castellón: a pilot study [PDF]
, 2019 Treball Final de Grau en Psicologia. Codi: PS1048. Curs: 2018/2019.Impulsivity is a characteristic symptom of adolescents with severe mental disorder and it has been related to difficulties in emotion regulation, social skills deficits and poor stress ...
Bernal Mohedano, Rafael
core
Propriedades psicométricas de uma escala para medir a gestão da vergonha em adolescentes (Moss-Sast) [PDF]
, 2015 (Ahmed, 1999) to measure shame management in adolescents in situations of aggression toward peers. The study was conducted with a sample of 700 students from public secondary schools (N= 700) located in a northwestern state municipality of Mexico ...
Carlos-Martínez, Ernesto Alonso +3 more
core +2 more sources
Libertad de expresión en Guanajuato durante 2015
Entretextos, 2016 El presente documento es una descripción de la situación de la libertad de expresión en Guanajuato durante 2015, incluye testimonios de periodistas y reflexiones en primera persona que el autor hace en función de su experiencia acompañando periodistas ...
José Raymundo Sandoval Bautista
doaj +1 more source
Reduced Muscular Carnosine in Proximal Myotonic Myopathy—A Pilot 1H‐MRS Study
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Myotonic dystrophy type 2 (proximal myotonic myopathy, PROMM) is a progressive multisystem disorder with muscular symptoms (proximal weakness, pain, myotonia) and systemic manifestations such as diabetes mellitus, cataracts, and cardiac arrhythmias.
Alexander Gussew +11 more
wiley +1 more source
Síndromes epilépticos en niños y adolescentes
Revista Médica Clínica Las Condes, 2013 En la edad pediátrica las epilepsias son frecuentes, con manifestaciones clínicas diversas y edad-dependientes. El reconocimiento preciso de los diferentes síndromes y epilepsias es importante para determinar un tratamiento y pronóstico adecuados.
López S. Isabel Margarita, Dra. +2 more
doaj +1 more source
Age‐Related Characteristics of SYT1‐Associated Neurodevelopmental Disorder
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objectives We describe the clinical manifestations and developmental abilities of individuals with SYT1‐associated neurodevelopmental disorder (Baker‐Gordon syndrome) from infancy to adulthood. We further describe the neuroradiological and electrophysiological characteristics of the condition at different ages, and explore the associations ...
Sam G. Norwitz +3 more
wiley +1 more source
Adolescentes activos e adolescentes sedentários : a realidade portuguesa
, 2010 Os comportamentos de lazer sedentários são muitas vezes associados à reduzida pratica de actividade física (AF) dos adolescentes. Esta investigação teve como grandes objectivos identificar os perfis de adolescentes, com base no tempo de que despendem diariamente a ver TV e a quantidade de vezes que praticam AF na semana, e compreender as variáveis ...
Marques de Loureiro, Nuno Eduardo +2 more
openaire +7 more sources
Entorno familiar y crianza del menor Wayuü trabajador del basurero de Riohacha-Colombia
Psicoespacios, 2018 El artículo presenta resultados de la investigación descriptiva transversal orientada a caracterizar el entorno familiar y prácticas de crianza en una muestra de las madres de los menores trabajadores del basurero de Riohacha- Guajira, Colombia.
Annabel Redondo Mendoza +2 more
doaj +1 more source
Developmental, Neuroanatomical and Cellular Expression of Genes Causing Dystonia
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Dystonia is one of the most common movement disorders, with variants in multiple genes identified as causative. However, an understanding of which developmental stages, brain regions, and cell types are most relevant is crucial for developing relevant disease models and therapeutics.
Darren Cameron +5 more
wiley +1 more source