Results 81 to 90 of about 4,622 (201)

Time of Exercise as Indicator of Quality Control in Ergometry Services [PDF]

open access: yes, 2014
Background:The search for quality requires assessment tools in the various subdivisions of a health complex. In diagnostic medicine, they are scarce and in ergometry suggestions of indicators were not found.Objective:To establish indicator for quality ...
Meneghelo, Romeu Sergio   +2 more
core   +3 more sources

Neurocirculatory distonia: diagnostics and treatment

open access: yesРоссийский кардиологический журнал, 2006
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O. N. Sivyakova, E. F. Konyuk
openaire   +1 more source

A Fatal Case of Generalized Lysosomal Storage Disease in an Infant. [PDF]

open access: yes, 2010
Gangliosidoses are a heterogeneous group of lysosomal storage diseases with an autosomal recessive trait, which are characterized by the intracellular accumulation of gangliosides in several tissues, mainly in neurons.
Ancer Rodríguez, Jesús   +7 more
core  

Estudo da imagem motora cinestésica em pacientes com cãibra do escrivão [PDF]

open access: yes, 2009
The aim was to determine if patients with writer' cramp (WC) have abnormalities in kinesthetic motor imagery of hand movements. We timed the execution and simulation of a "finger tap task" and a "writing task" in 9 patients with simple WC and 9 matched ...
SAKAMOTO, Americo C., TUMAS, Vitor
core   +2 more sources

Distonia de torção: Antonio de Moraes Austregésilo Filho [PDF]

open access: yesArquivos de Neuro-Psiquiatria, 1945
O A. analisa, inicialmente, com minucia, os trabalhos de Ziehen, Schwalbe, Oppenheim, Thomalla, assim como os de Hall e Wimmer, referindo-se cronologicamente a todos os que contribuiram para o esclarecimento do assunto. Destaca-se nesta revisao bibliografica a contribuicao brasileira que se fez sentir com os trabalhos de Rocha Vaz e J. Carvalho (1912),
openaire   +2 more sources

ePresentation

open access: yes
European Journal of Neurology, Volume 32, Issue S1, June 2025.
wiley   +1 more source

A novel missense mutation pattern of the GCH1 gene in dopa-responsive dystonia Novo padrão de mutação missense no gene GCH1 na distonia dopa-responsiva

open access: yesArquivos de Neuro-Psiquiatria, 2007
Dopa-responsive dystonia (DRD) is an inherited metabolic disorder now classified as DYT5 with two different biochemical defects: autosomal dominant GTP cyclohydrolase 1 (GCH1) deficiency or autosomal recessive tyrosine hydroxylase deficiency.
Rosana H. Scola   +6 more
doaj   +1 more source

The importance of a physical activity program for patients with multiple sclerosis on life satisfaction and psychological well-being [PDF]

open access: yes, 2013
A Esclerose Múltipla (EM) é uma doença crónica do sistema nervoso central, que afeta com mais frequentemente mulheres jovens. A EM é uma doença progressiva e imprevisível, resultando em alguns casos de incapacidades e limitações a nível físico ...
Pais-Ribeiro, José Luís   +2 more
core  

ePoster

open access: yes
European Journal of Neurology, Volume 32, Issue S1, June 2025.
wiley   +1 more source

Dopa-sensitive progressive dystonia of childhood with diurnal fluctuations of symptoms: a case report

open access: yesArquivos de Neuro-Psiquiatria, 1995
Progressive dystonia with diurnal fluctuations sensitive to levodopa, also known as Segawa's disease, is a rare form of autosomal dominant extrapyramidal disease in the pediatric age group.
José Luiz Dias Gherpelli   +2 more
doaj   +1 more source

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