Results 11 to 20 of about 118 (101)

Relief of primary cervical dystonia symptoms by low frequency transcranial magnetic stimulation of the premotor cortex: case report Alívio da distonia cervical primária com o uso da estimulação magnética transcraniana de baixa freqüência sobre o córtex pré-motor: relato de caso

open access: yesArquivos de Neuro-Psiquiatria, 2007
OBJECTIVE: To evaluate the effect of low-frequency repetitive transcranial magnetic stimulation (rTMS) on the symptoms of a patient with primary segmental dystonia (PSD).
Nasser Allam   +5 more
doaj   +3 more sources

Aplicación de toxina botulínica en el tratamiento de la distonía. Experiencia en un hospital de tercer nivel

open access: yesRevista Colombiana de Medicina Física y Rehabilitación, 2022
Introducción. La distonía es un trastorno del movimiento que produce afectaciones funcionales a quienes la padecen; la aplicación de toxina botulínica es el tratamiento de elección debido a su seguridad. Objetivo.
Yudi Milena Rodriguez Mojica   +2 more
doaj   +3 more sources

Distonia Cervical e Tremor Distónico Atípico de Provável Etiologia Traumática

open access: yesArquivos de Neuro-Psiquiatria, 2007
A distonia cervical pós-traumática é uma sequela rara do traumatismo crânio-encefálico. Os autores descrevem o caso clínico de um doente com distonia cervical e movimentos involuntários sugestivo de tremor distónico que surgiram após um traumatismo cefálico.
Silva,Ana Isabel   +3 more
openaire   +5 more sources

Toxina botunílica tipo B no manejo de distonia não-responsiva a toxina botunílica tipo A [PDF]

open access: yesArquivos de Neuro-Psiquiatria, 2003
Injeção de toxina botulínica (BTX) é o tratamento de escolha para distonias focais. Contudo, 10% ou mais dos pacientes que recebem injeções repetitivas de BTX tipo A (BTX-A) perdem resposta (não-respondedores secundários).
Francisco Cardoso
doaj   +1 more source

Genetic evaluation for TOR1-A (DYT1) in Brazilian patients with dystonia

open access: yesArquivos de Neuro-Psiquiatria, 2014
Several genes have been mapped in families or in sporadic cases of dystonia. TOR1-A (DYT1) gene was linked to isolated dystonia. Objective To associate clinical information of patients with dystonia with the TOR1-A gene mutations.
Carlos Henrique F. Camargo   +4 more
doaj   +1 more source

Does sex influence age at onset in cranial-cervical and upper limb dystonia? [PDF]

open access: yesJournal of Neurology, Neurosurgery & Psychiatry, 2003
The relation between age at dystonia onset and sex was investigated in 264 patients with cranial-cervical dystonia and 56 patients with upper limb dystonia. In cranial-cervical dystonia, women had a significantly greater age at the onset of dystonia than men. The association was independent of duration of disease and distance of referral, but it was no
DEFAZIO G   +11 more
openaire   +6 more sources

Cervical dystonia: about familial and sporadic cases in 88 patients

open access: yesArquivos de Neuro-Psiquiatria, 2014
Cervical dystonia (CD) affects the musculature of the neck in a focal way or associated to other parts of the body. The aim of this study was to identify clinical differences between patients with dystonia patients without family history and with family ...
Carlos Henrique F. Camargo   +6 more
doaj   +1 more source

Toxina botulínica no tratamento do torcicolo espasmódico: uma meta-análise

open access: yesArquivos de Neuro-Psiquiatria, 1994
Os autores fizeram uma meta-análise da literatura sobre o uso da toxina botulínica no tratamento do torcicolo espasmódico. Concluem que a toxina botulínica é uma medida terapêutica eficaz para a distonia cervical.
Sérgio Carlos Morais Teixeira   +2 more
doaj   +1 more source

Role of the dopamine D5 receptor (DRD5) as a susceptibility gene for cervical dystonia [PDF]

open access: yesJournal of Neurology, Neurosurgery & Psychiatry, 2003
Cervical dystonia (CD) is one of the most common forms of primary dystonia. The pathogenesis of the disease is still unknown, although evidence suggests a role for genetic factors. Recently, a polymorphism in the dopamine D5 receptor (DRD5) gene has been associated with the disease in a British population, suggesting that DRD5 is a susceptibility gene ...
F. BRANCATI   +13 more
openaire   +8 more sources

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