1999
DOI: 10.1016/s0022-510x(99)00143-4
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A prospective study on the natural history of multiple sclerosis: clues to the conduct and interpretation of clinical trials

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Cited by 118 publications
(103 citation statements)
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“…She suffered additional neurologic impairment as a result of this traumatic hemorrhage confounding further assessment of any treatment. Her platelet count at the time of the injury was 88 000/mm 3 . This patient went on to develop progressive neurologic deterioration and died 18 months following the procedure.…”
Section: Safetymentioning
confidence: 99%
See 1 more Smart Citation
“…She suffered additional neurologic impairment as a result of this traumatic hemorrhage confounding further assessment of any treatment. Her platelet count at the time of the injury was 88 000/mm 3 . This patient went on to develop progressive neurologic deterioration and died 18 months following the procedure.…”
Section: Safetymentioning
confidence: 99%
“…Over time most such patients eventually develop secondary progressive disease manifested as gradual neurologic impairment often progressing without acute relapses, although acute relapses may persist. [2][3][4][5][6] Natural history studies show that by 15 years following disease onset, at least 50%, and by 30 years at least 80%, of subjects lose the ability to ambulate without support. [6][7][8][9] Neurologic disability is defined at 0.5-step increments by the expanded disability status scale (EDSS) from zero (no disability) to 10.0 (death related to neurologic progression).…”
Section: Introductionmentioning
confidence: 99%
“…Indeed, frequency of cognitive dysfunction is high in MS, present in nearly half of patients, as soon as at the early stage of the disease, even in subjects with low disability [Amato et al, 1999;Bagert et al, 2002;Dujardin et al, 1998;Rao et al, 1991]. Dysfunction frequently concerns information processing speed and recall of recently learned verbal or visual information, one aspect of memory [Amato et al, 1999;Bagert et al, 2002;Dujardin et al, 1998;Rao et al, 1991].…”
Section: Introductionmentioning
confidence: 99%
“…18 les symptômes associés à une poussée, comme les troubles moteurs plutôt que sensoriels et la localisation des lésions à l'origine d'une poussée, peuvent constituer d'importants facteurs pronostiques. il a été constaté une association faible entre les troubles sensitifs et l'évolution de la SEP [19][20][21] . une poussée de névrite optique est plus favorable qu'une ataxie grave, qui a été associée à des poussées multiples 22 .…”
Section: Indicateurs Cliniques De L'évolution De La Maladieunclassified