Search Results - "Lobjois, Quentin"

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    NMOSD-like and longitudinal extensive HTLV1-associated myelitis are extremes that flank an overlooked continuum by Bonnan, Mickael, Olindo, Stéphane, Signate, Aissatou, Lobjois, Quentin, Stephant, Maeva, Boulos, Dalia Dimitri, Cabre, Philippe

    “…Background HTLV1-associated myelitis (HAM) is a slowly progressive myelopathy in which spinal cord MRI demonstrates no lesion or atrophy. Objective We examined…”
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    Journal Article
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    Mitoxantrone in NMO Spectrum Disorder in a Large Multicenter Cohort in French Caribbean by Chaumont, Hugo, Bérard, Nicolas, Karam, Jean-Pierre, Lobjois, Quentin, Tressieres, Benoit, Signate, Aissatou, Lannuzel, Annie, Cabre, Philippe

    “…BACKGROUND AND OBJECTIVESPreventing relapses in neuromyelitis Optica spectrum disorder (NMOSD) is a primary goal. New effective molecules are often expensive…”
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  5. 5

    When electrodiagnosis for tremor reveals a rare peripheral disease by Lobjois, Quentin, Mongin, Marie, Worbe, Yulia, Dussaule, Jean Claude, Salachas, François, Apartis, Emmanuelle

    Published in Neurophysiologie clinique (01-06-2018)
    “…Spinal and bulbar muscular atrophy (SBMA) (or Kennedy's disease) is a rare X-linked neurodegenerative disorder associated with limb and bulbo-facial paresis,…”
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    Efficacité et tolérance de la Mitoxantrone dans une cohorte multicentrique de patients atteints de maladies du spectre de la neuromyélite optique (NMOSD) aux Antilles françaises by Berard, Nicolas, Chaumont, Hugo, Karam, Jean-Pierre, Lobjois, Quentin, Signaté, Aissatou, Lannuzel, Annie, Cabre, Philippe

    Published in Revue neurologique (01-04-2024)
    “…Dans les pathologies du spectre de la neuromyélite optique (NMOSD), la prévention de nouvelles poussées inflammatoires est fondamentale. Les nouvelles…”
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    Journal Article
  9. 9

    NeuroBehçet: un cas d’agrégation familiale chez des jumeaux monozygotes by Bourgeois, Quentin, Lobjois, Quentin, Signaté, Aissatou, Cabre, Philippe

    Published in Revue neurologique (01-04-2021)
    “…La maladie de Behçet (MDB) est liée en partie à des facteurs génétiques. Des symptômes neurologiques sont fréquemment retrouvés. Nous rapportons le premier cas…”
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    Journal Article