Browsing by Author Vallat, Jean-Michel

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Issue DateTitleAuthor(s)Citation
2016Contactin-Associated Protein 1 (CNTNAP1) Mutations Induce Characteristic Lesions of the Paranodal RegionOuvrier, Robert; Cogne, Benjamin; Devaux, Jerome; Isidor, Bertrand; Magee, A; Magy, Laurent; Mathis, Stephane; Nizon, Mathilde; Pereon, Yann; Richard, Laurence; Vallat, Jean-Michel; Zuchner, Stephan; Childrens Hospital Westmead: Paediatrics & Child HealthContactin-Associated Protein 1 (CNTNAP1) Mutations Induce Characteristic Lesions of the Paranodal Region, Journal of Neuropathology and Experimental Neurology, vol.75, 12, 2016,pp 1155-1159
2006Expression of the antioxidant enzyme peroxiredoxin 5 in the human peripheral nervous system.Lu, Jun; Ouvrier, Robert; Pollard, John; knoops, Bernard; Vallat, Jean-Michel; Central Clinical School: Medicine; Children's Hospital Westmead: Paediatrics & Child Health; Central Clinical School: MedicineExpression of the antioxidant enzyme peroxiredoxin 5 in the human peripheral nervous system., Journal of the Peripheral Nervous System, vol.11,(4),2006,pp 318-324
2008Histopathological Findings in Hereditary Motor and Sensory Neuropathy of Axonal Type With Onset in Early Childhood Associated With Mitofusin 2 Mutations.Nicholson, Garth; Zhu, Danqing; Funalot, Benoit; Grew, S; Magdelaine, C; Ouvrier, Robert A.; Pollard, John D; Ryan, Monique M.; Vallat, Jean-Michel; Concord Clinical School: ANZAC Research Institute; Concord Clinical School: MedicineHistopathological Findings in Hereditary Motor and Sensory Neuropathy of Axonal Type With Onset in Early Childhood Associated With Mitofusin 2 Mutations., Journal of neuropathology and experimental neurology, vol.67,(11),2008,pp 1097-1102
2010Intramuscular Interferon Beta-1a in Chronic Inflammatory Demyelinating PolyradiculoneuropathyPollard, John; Cros, Didier P.; Davar, G.; Dawson, K.; Gorson, K. C.; Griffin, John W.; Hughes, R. A. C.; Maurer, S L; Riester, K.; Sandrock, A.; Vallat, Jean-Michel; Central Clinical School: MedicineIntramuscular Interferon Beta-1a in Chronic Inflammatory Demyelinating Polyradiculoneuropathy, Neurology, vol.74, 8,pp 651-657
2008Severe early-onset axonal neuropathy with homozygous and compound heterozygous MFN2 mutationsNicholson, Garth; Zhu, Danqing; Grew, S; Magdelaine, C; Ouvrier, Robert; Ryan, M; Sturtz, F; Vallat, Jean-Michel; Concord Clinical School: ANZAC Research Institute; Concord Clinical School: MedicineSevere early-onset axonal neuropathy with homozygous and compound heterozygous MFN2 mutations, Neurology, vol.70, 19, 2008,pp 1678-1681