Zobrazeno 1 - 10
of 21
pro vyhledávání: '"J P, Borsotti"'
Publikováno v:
Rheumatology. 42:349-352
Objective. To clarify the association between parvovirus B19 and myositis. Methods. Biopsy samples of muscle from eight patients with inflammatory myopathies were studied for the presence of B19 DNA by polymerase chain reaction. Expression of VP1 and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10dad8ba3dc9bc944e0b7f5058beb76d
https://doi.org/10.1093/rheumatology/keg085
https://doi.org/10.1093/rheumatology/keg085
Akademický článek
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Autor:
Maingon P, Billiar T, M. Giroud, J. P. Borsotti, D'Athis P, R. Dumas, Janoray P, Sautreaux Jl
Publikováno v:
Neurological Research. 21:171-174
The aim of this study was to provide current data on case-fatality rates of malignant gliomas in the area of Burgundy (1,300,000 inhabitants). The ascertainment was specific according to imaging and histologic criteria, and was exhaustive because of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52da8b33d51d8e0fb82468985cfce941
https://doi.org/10.1080/01616412.1999.11740913
https://doi.org/10.1080/01616412.1999.11740913
Publikováno v:
Revue neurologique. 152(6-7)
Dysembryoplastic neuroepithelial tumor (DNT) is a newly recognized brain lesion first reported in 1988 by Daumas-Duport et al. The authors described five cases of DNT, that occurred in young people and were characterized by partial seizures. Seizures
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9168df753893a2ade63f5f030118151e
https://pubmed.ncbi.nlm.nih.gov/8944242
https://pubmed.ncbi.nlm.nih.gov/8944242
Publikováno v:
Annales de cardiologie et d'angeiologie. 44(3)
Analysis of 109 well documented cases of permanent total atrial paralysis reported in the literature illustrated the features of this arrhythmia which is a well defined entity consisting of suppression of all electrical and mechanical activity of bot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::579e80eeccef0d001d83d32bceb1902f
https://pubmed.ncbi.nlm.nih.gov/7793852
https://pubmed.ncbi.nlm.nih.gov/7793852
Publikováno v:
Revue neurologique. 148(3)
A 37 year-old man sustained 2 ischemic strokes during acute alcohol intoxication. One month after the onset of strokes, a spontaneous atrial flutter occurred. Autopsy revealed an embolic rostral occlusion of the basilar artery. Cardiac verification d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::098f581d297703eb0255a6f790f4a6ee
https://pubmed.ncbi.nlm.nih.gov/1604137
https://pubmed.ncbi.nlm.nih.gov/1604137
Publikováno v:
Pediatrie. 46(12)
In an investigation of 15 patients with Duchenne muscular dystrophy, the authors found mental retardation in all cases. In addition, CT scan showed a cortical atrophy after the age of 10 years. This finding suggests that a cerebral degenerative proce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::228ba493e949ea7f6341c85f80b2b2ab
https://pubmed.ncbi.nlm.nih.gov/1667037
https://pubmed.ncbi.nlm.nih.gov/1667037
Publikováno v:
Revue neurologique. 146(4)
We report 3 cases of epilepsy with bilateral occipital calcifications followed up for several years. These cases were compared with 21 published cases and were found to differ from the classical Sturge-Weber syndrome on several points: 1) the disease
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bc7b372ee2cff3aeae41c4fec757038a
https://pubmed.ncbi.nlm.nih.gov/2193337
https://pubmed.ncbi.nlm.nih.gov/2193337
Akademický článek
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Publikováno v:
La Revue de Médecine Interne. 10:471-474
A clinical history typical of multisclerosis began in a 20-year old man with transient, then permanent manifestations involving the optic tract and the pyramidal, extrapyramidal and cerebellar systems. The patient died at the age of 62, at the end-st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::290124a279bd8d43ef50b0502d852ff1
https://doi.org/10.1016/s0248-8663(89)80058-x
https://doi.org/10.1016/s0248-8663(89)80058-x