Zobrazeno 1 - 10
of 98
pro vyhledávání: '"Henri Petit"'
Publikováno v:
Alzheimer Disease & Associated Disorders. 12:335-339
At autopsy, frontotemporal dementia (FTD) account for up to 20% of degenerative dementia cases, although FTDs are underrecognized in memory clinics. FTDs are confused with Alzheimer disease (AD) or vascular dementia (VaD). These misdiagnosis may affe
Publikováno v:
International Journal of Geriatric Psychiatry. 13:516-519
Background. Response to tacrine varies among patients with Alzheimer's disease (AD). Lewy body dementia (LBD) could be a high responder subtype of AD. The aim of the study was to compare the effects of tacrine in LBD and AD. Methods. Seventy-five con
Autor:
Philippe Remy, Marc Steinling, Godefroy O, Henri Petit, Caparros-Lefebvre D, Cabaret M, Yves Samson
Publikováno v:
Journal of Neural Transmission. 105:489-495
A 76-year old woman was affected by lethargic encephalitis in 1918, at the age of 3 months. Long-term clinical follow-up with late neuropsychological evaluation revealed post-encephalitic parkinsonism, which worsened very slowly and was improved by l
Publikováno v:
Dementia and Geriatric Cognitive Disorders. 9:99-102
In our memory clinic experience, memory impairment differs widely in patients with frontotemporal dementia (FTD). We searched for a correlation between explicit memory disturbance assessed with the Grober and Buschke test and medial temporal atrophy
Autor:
Patrick Vermersch, H. Hofmann-Radvanyi, Henri Petit, Nicolas Sergeant, André Delacourte, A. Wattez, Ph. Dewailly, Marie-Magdeleine Ruchoux
Publikováno v:
Neurology. 47:711-717
The mutation causing myotonic dystrophy (DM) is an unstable CTG trinucleotide repeat in a gene encoding for a protein with putative serine-threonine kinase activity. Several studies have reported the appearance of abnormally frequent neurofibrillary
Autor:
Christine Daems-Monpeurt, Jean Dallongeville, Didier Lefranc, André Delacourte, Patrick Vermersch, Henri Petit
Publikováno v:
Neuroscience Letters. 212:91-94
Apolipoprotein E (Apo E), one of the major structural and functional apolipoproteins, has recently been implicated in the pathogenesis of Alzheimer's disease (AD). Several studies revealed that Apo E4 isoform is associated with the pathogenic process
Publikováno v:
La Revue de Médecine Interne. 17:482-487
Resume Les atteintes centrales hemispheriques de la neurosarcoidose sont considerees comme rares. Leur polymorphisme clinique et radiologique rend compte des difficultes diagnostiques. Grâce a l'imagerie par resonance magnetique (IRM), le diagnostic
Autor:
Andrié Grimaldi, Martine Remy, Dominique Caparros-Lefebvre, Bernard Brun, Catherine Veyssier-Belot, Benoît Wallaert, Pierre Godeau, Bertrand Wechsler, Henri Petit, Patrice Cacoub, Janine Wechsler
Publikováno v:
Medicine. 75:157-169
We made a retrospective evaluation of clinical and radiologic features, treatment, and outcome of Erdheim-Chester disease, a rare non-Langerhans cell histiocytosis. We had 7 patients coming from 3 French teaching hospitals and reviewed 52 cases from
Publikováno v:
Archives of Gerontology and Geriatrics. 22:49-54
Characterisation of sundowning syndrome, defined as 'an exacerbation of symptoms indicating increased arousal or impairment in late afternoon, evening or at night, among elderly demented individuals', is complicated by neuroleptic therapy and frequen