Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Mais filtros










Base de dados
Intervalo de ano de publicação
1.
J Sleep Res ; 4(2): 119-130, 1995 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-28849872

RESUMO

Although various investigators have suggested algorithms for the automatic detection of eye movements during sleep, objective comparisons of the proposed methods have previously been difficult due to different recording arrangements of different investigators. In this study the results of five eye movement detection algorithms applied to the same data were compared to visually scored data. The percentages of true and false detections are given for various threshold levels in rapid and slow eye movement detections. The methods gave best results when they were used with the same electrode montage they were designed for but the performance decreased when other montages were used. Subtracting the cross-talk of EEG delta activity improved the correctness of eye movement detections.

2.
Vet Pathol ; 9(5): 328-349, 1972 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-29884006

RESUMO

Five male Irish Terrier puppies had a stiff gait, difficulty in swallowing, dirty cheeks because of food residues, an enlarged tongue and atrophic muscles. At electromyographical examination high-frequency discharges suggestive of myotonia were present. The values for serum creatine-phosphokinase and aldolase were extremely high. Serum vitamin E values were normal. At necropsy the muscles were pale with yellowish white streaks. Histologically there was a patchy distribution of the lesions. Granular and floccular changes (Zenker's degeneration) with phagocytosis, giant cells and calcification were found. Histochemical changes were the same in all muscles investigated, but were not equally pronounced. In the muscle specimens with greatest change the distinction between type I and type II fibres was largely lost. Rounded hypertrophic fibres contained no glycogen, and most did not show activity of phosphorylase, dehydrogenases, and oxidases. Activity of glyccrol-3-phosphate oxidase and acid phosphatase was markedly increased. Abnormal mitochondria and unknown electron-dense bodies were found. The tubular system seemed to be reduced in some abnormal fibres. The disease is probably recessive X-linked.

SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...