Search Results - "WOIMANT, F"

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  1. 1

    Prospective study of symptomatic atherothrombotic intracranial stenoses : The GESICA study by MAZIGHI, M, TANASESCU, R, DUCROCQ, X, VICAUT, E, BRACARD, S, HOUDART, E, WOIMANT, F

    Published in Neurology (25-04-2006)
    “…Symptomatic intracranial atherothrombotic stenoses (ICAS) are associated with high rates of cerebrovascular ischemic events. To conduct a prospective…”
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    Journal Article
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    Exchangeable copper: a reflection of the neurological severity in Wilson's disease by Poujois, A., Trocello, J.‐M., Djebrani‐Oussedik, N., Poupon, J., Collet, C., Girardot‐Tinant, N., Sobesky, R., Habès, D., Debray, D., Vanlemmens, C., Fluchère, F., Ory‐Magne, F., Labreuche, J., Preda, C., Woimant, F.

    Published in European journal of neurology (01-01-2017)
    “…Background and purpose The severity of Wilson's disease (WD) is linked to free copper accumulating in the liver and brain. Exchangeable copper (CuEXC) is a new…”
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    Cost of stroke in France by Chevreul, K., Durand-Zaleski, I., Gouépo, A., Fery-Lemonnier, E., Hommel, M., Woimant, F.

    Published in European journal of neurology (01-07-2013)
    “…Background and purpose A cost of illness study was undertaken on behalf of the French Ministry of Health to estimate the annual cost of stroke in France with…”
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    Regional disparities in acute and post-acute care of stroke patients in France, 2015 by de Peretti, C., Gabet, A., Lecoffre, C., Oberlin, P., Olié, Valérie, Woimant, F.

    Published in Revue neurologique (01-09-2018)
    “…The aim of this study was to assess regional variations of the hospital management of stroke patients during acute and post-acute phases in France in 2015…”
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    The hidden face of Wilson's disease by Woimant, F., Djebrani-Oussedik, N., Collet, C., Girardot, N., Poujois, A.

    Published in Revue neurologique (01-11-2018)
    “…In brief, the classic form of Wilson's disease (WD) is an autosomal-recessive condition with hepatic, neurologic, psychiatric and systemic manifestations…”
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    Management and 2-year follow-up of children aged 29 days to 17 years hospitalized for a first stroke in France (2009-2010) by TUPPIN, P, SAMSON, S, WOIMANT, F, CHABRIER, S

    “…Childhood stroke is a little-known disease in France. The objective of this study was to report the characteristics, management, treatment and outcome of…”
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    Care pathways and healthcare use of stroke survivors six months after admission to an acute-care hospital in France in 2012 by Tuppin, P., Samson, S., Fagot-Campagna, A., Woimant, F.

    Published in Revue neurologique (01-04-2016)
    “…Care pathways and healthcare management are not well described for patients hospitalized for stroke. Among the 51 million beneficiaries of the French national…”
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    Bone status and fractures in 85 adults with Wilson’s disease by Quemeneur, A.-S., Trocello, J.-M., Ea, H.-K., Ostertag, A., Leyendecker, A., Duclos-Vallée, J.-C., de Vernejoul, M.-C., Woimant, F., Lioté, F.

    Published in Osteoporosis international (01-11-2014)
    “…Summary Wilson’s disease is characterized by copper deposition, especially in the liver and central nervous system. We assessed the prevalent fractures and…”
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    Compliance with treatment in Wilson's disease: On the interest of a multidisciplinary closer follow-up by Jacquelet, E, Beretti, J, De-Tassigny, A, Girardot-Tinant, N, Wenisch, E, Lachaux, A, Pheulpin, M-C, Poujois, A, Woimant, F

    Published in La revue de medecine interne (01-03-2018)
    “…Compliance with treatment is very important for patients who suffer from Wilson's disease, a rare genetic disorder. They can benefit a long-life and effective…”
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    Cognitive profile in Wilson's disease: A case series of 31 patients by Wenisch, É., De Tassigny, A., Trocello, J.-M., Beretti, J., Girardot-Tinant, N., Woimant, F.

    Published in Revue neurologique (01-12-2013)
    “…Wilson's disease (WD) is a rare autosomal recessive disorder of copper metabolism. If untreated, WD, which is initially a liver disease, can turn into a…”
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    Samuel Alexander Kinnier Wilson. Wilson's disease, Queen Square and neurology by Broussolle, E., Trocello, J.-M., Woimant, F., Lachaux, A., Quinn, N.

    Published in Revue neurologique (01-12-2013)
    “…This historical article describes the life and work of the British physician Samuel Alexander Kinnier Wilson (1878–1937), who was one of the world's greatest…”
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    Clinical correlates of cerebral water diffusion in Wilson disease by FAVROLE, P, CHABRIAT, H, GUICHARD, J. P, WOIMANT, F

    Published in Neurology (14-02-2006)
    “…To investigate the course of diffusion changes in Wilson disease (WD) and to evaluate their clinical and radiologic correlates. MRI with fluid-attenuated…”
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    Ocular motility and Wilson’s disease: a study on 34 patients by Ingster-Moati, I, Bui Quoc, E, Pless, M, Djomby, R, Orssaud, C, Guichard, J P, Woimant, F

    “…Background:Wilson’s disease is an autosomal recessive genetic disorder resulting from an abnormality of copper metabolism. The excessive accumulation of copper…”
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    First hospitalization for transient ischemic attack in France: Characteristics, treatments and 3-year outcomes by Cosker, K., Samson, S., Fagot-Campagna, A., Woimant, F., Tuppin, P.

    Published in Revue neurologique (01-02-2016)
    “…Characteristics of patients hospitalized for transient ischemic attack (TIA) management before and during this hospitalization and follow-up are not well…”
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    Prevalence of self-reported stroke and disability in the French adult population: A transversal study by Schnitzler, A., Dr, Tuppin, P., Dr, Woimant, F., Dr

    “…Background In France, the prevalence of stroke and the level of disability of stroke survivors are little known. The aim of this study was to evaluate…”
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    A hereditary moyamoya syndrome with multisystemic manifestations by HERVE, D, TOURAINE, P, METZGER, J. P, TOURNIER-LASSERVE, E, WOIMANT, F, VERLOES, A, MISKINYTE, S, KRIVOSIC, V, LOGEART, D, ALILI, N, LAREDO, J. D, GAUDRIC, A, HOUDART, E

    Published in Neurology (20-07-2010)
    “…We report a detailed description of a family affected by a hereditary multisystem disorder associated with moyamoya syndrome. In this family case report, we…”
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    Corpus callosum abnormalities in Wilson's disease by Trocello, J M, Guichard, J P, Leyendecker, A, Pernon, M, Chaine, P, El Balkhi, S, Poupon, J, Chappuis, P, Woimant, F

    “…IntroductionWilson's disease (WD) with neurological presentation is associated with brain lesions classically localised in globus pallidus, putamen, thalamus,…”
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