Results 31 to 40 of about 21,127 (173)

Extreme spindles in magnetic resonance age: clinical and neurphysiological and neuroimaging characteristics [PDF]

open access: yes, 2005
OBJECTIVES: Extreme spindles were described by Gibbs and Gibbs in 1962. They are typically observed in children younger than five years, occurring in 0.05% of normal children and in up to 5 to 18% of children with mental retardation or cerebral palsy. In
Caboclo, Luís Otávio Sales Ferreira   +5 more
core   +3 more sources

Vigabatrina no tratamento da síndrome de West: avaliação clínica e eletrencefalográfica em 13 pacientes Treatment of West syndrome with vigabatrin: clinical and electroencephalographic evaluation of 13 patients

open access: yesArquivos de Neuro-Psiquiatria, 2007
Avaliamos a eficácia da vigabatrina (VGB) como monoterapia inicial para síndrome de West (SW), os seus efeitos colaterais e a evolução a curto prazo do eletrencefalograma (EEG), num estudo prospectivo, aberto e não controlado.
Adélia Maria de Miranda Henriques-Souza   +2 more
doaj   +1 more source

Uso clínico de Vigabatrín en epilepsia

open access: yesActa Neurológica Colombiana, 2023
El Vigabatrin (VGB) es un medicamento anticonvulsivante cuyo uso en epilepsia se conoce desde hace tres décadas, está indicado en el control de crisis parciales complejas en epilepsias focales refractarias y en espasmos infantiles, especialmente los ...
Daniel Nariño, Carolina Ruiz de S
doaj   +2 more sources

Application of integrated perturbation index and articulatory precision index in patients with spasmodic dysphonia [PDF]

open access: yes, 2014
La disfonía espasmódica es un desorden vocal severo caracterizado por una interrupción involuntaria de la fonación, denominada también distonía focal laríngea.
Gurlekian, Jorge Alberto, Sigal, Liliana
core  

Tonic spasms are a common clinical manifestation in patients with neuromyelitis optica Espasmos tônicos são manifestações clínicas frequentes em pacientes com neuromielite óptica

open access: yesArquivos de Neuro-Psiquiatria, 2013
Tonic spasms have been most commonly associated with multiple sclerosis. To date, few reports of series of patients with neuromyelitis optica and tonic spasms have been published.
Luz Abaroa   +5 more
doaj  

Síndrome de west em gêmeos univitelinos

open access: yesArquivos de Neuro-Psiquiatria, 1990
Os autores registram os casos de dois gêmeos univitelinos com 6 meses de idade, do sexo masculino, com quadro de espasmos em flexão. O EEG nas duas crianças é idêntico, mostrando hipsarritmia.
Edson Zerati, Antônio Seba Junior
doaj   +1 more source

Effects of whole-body vibration training in patients with multiple sclerosis: A systematic review [PDF]

open access: yes, 2016
Introduction Multiple sclerosis (MS) is an autoimmune inflammatory disease of the central nervous system. MS is characterised by nerve demyelination that can alter nerve transmission and lead to such symptoms as fatigue, muscle weakness, and impaired ...
Castillo Bueno, I.   +2 more
core   +2 more sources

Tratamiento de espasmos masivos con ACTH sintético [PDF]

open access: yesRevista chilena de pediatría, 1991
Ten infants with infantile spasms (IS) and hypsarrhytmic EEC, received 0.5 mg i.m. of synthetic ACTH, three times a week for 2 weeks. Six of them showed complete remission of seizures and dramatical EEG changes, and 3 cases resulted in a partial response. Spasms were controlled during the first week in 5/6 cases where treatment was successful.
Lopez S, Isabel   +3 more
openaire   +2 more sources

Síndrome de West: reporte de un caso.

open access: yesMedicina Clínica y Social, 2020
Introducción: es una encefalopatía epiléptica dependiente de la edad caracterizada por la tríada electroclínica de espasmos epilépticos, retardo del desarrollo psicomotor y patrón electroencefalográfico de hipsarritmia en el electroencefalograma ...
Carlos Miguel Ríos-González
doaj  

Introducción del sistema PECS para la superación de las limitaciones comunicativas en un caso de síndrome de West [PDF]

open access: yes, 2016
En este estudio de caso se aborda la intervención realizada en una alumna de cuatro años, escolarizada en un aula específica de un centro ordinario, y a la que recientemente han diagnosticado síndrome de West.
Peirats Chacón, José   +1 more
core   +1 more source

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