P50 Genetics of riboflavin channels von Manole, A.A, Pandraud, A, Houlden, H

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Mitochondrial dysfunction in a treatable childhood neuronopathy von Manole, A, Jaunmuktane, Z, Pandraud, A, Hanna, M.G, Reilly, M.M, Kullmann, D.M, Jepson, J.E.C, Houlden, H

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P49 Mitochondrial abnormalities and increased oxidative stress in HSBP1iinduced distal hereditary motor neuropathies von Kalmar, B, Kolaszynska, A. Koyen, Rossor, A, Pandraud, A, Reilly, M, Greensmith, L

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Genetic screening of Greek patients with Huntington's disease phenocopies identifies an SCA8 expansion von Koutsis, G., Karadima, G., Pandraud, A., Sweeney, M. G., Paudel, R., Houlden, H., Wood, N. W., Panas, M.

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P56 Whole-exome sequencing in patients with sensory and motor inherited neuropathies von Horga, A, Cottenie, E, Liu, Y-T, Pandraud, A, Rossor, A.M, Pitceathly, R.D.S, Laurá, M, Hanna, M.G, Houlden, H, Reilly, M.M

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Mutational analysis of PMP22, EGR2, LITAF and NEFL in Greek Charcot-Marie-Tooth type 1 patients von Koutsis, G, Pandraud, A, Karadima, G, Panas, M, Reilly, MM, Floroskufi, P, Wood, NW, Houlden, H

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P43 Genetic modifying factors for the common form of CMT1A due to the chromosome 17 duplication and other causes of CMT1 in non-CMT1A patients von Pandraud, A, Murphy, S.M, Laurá, M, Reilly, M.M, Houlden, H

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P48 Genetic and functional investigation of Brown-Vialetto-Van Laere syndrome and related neuropathies von Pandraud, A, Johnson, J.O, Singleton, A.B, Clayton, P, Land, J, Hargreaves, I, Foley, A.R, Muntoni, F, Reilly, M.M, Houlden, H

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O03 High-dose riboflavin therapy in Brown-Vialetto-Van Laere syndrome: clinical and biochemical improvement von Foley, A.R, Broomfield, A.A, Pandraud, A, Johnson, J.O, Singleton, A.B, Hargreaves, I.P, Land, J.M, Grunewald, S, Rahman, S, Clayton, P, Houlden, H, Reilly, M.M, Muntoni, F

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PN03 - Mitochondrial dysfunction in a treatable childhood neuronopathy von Manole, A., Jaunmuktane, Z., Pandraud, A., Hanna, M.G., Reilly, M.M., Kullmann, D.M., Jepson, J.E.C., Houlden, H.

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Novel peripheral myelin protein 22 (PMP22) micromutations associated with variable phenotypes in Greek patients with Charcot-Marie-Tooth disease von Koutsis, Georgios, Pandraud, Amelie, Polke, James M, Wood, Nicholas W, Panas, Marios, Karadima, Georgia, Houlden, Henry

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A Genetic and Functional Investigation of Inherited Neuropathies: Charcot-Marie Tooth Disease and Brown-Vialetto-Van Laere Syndrome von Pandraud, A

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1030 Charcot-Marie-tooth disease: genetic diagnoses in a specialist clinic von Murphy, S, Pandraud, A, Liu, Y, Fawcett, K, Polke, J M, Davidson, G, Laura, M, Davis, M, Houlden, H, Reilly, M M

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EBC Annex 71: Building Energy Performance Assessment Based on In-situ Measurements von Fitton, Richard

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Madras motor neuron disease (MMND) is distinct from the riboflavin transporter genetic defects that cause Brown-Vialetto-Van Laere syndrome von Nalini, A, Pandraud, A, Mok, K, Houlden, H

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Mitochondrial deficits and abnormal mitochondrial retrograde axonal transport play a role in the pathogenesis of mutant Hsp27 induced Charcot Marie Tooth Disease von Kalmar, B, Innes, A, Wanisch, K, Koyen Kolaszynska, A, Pandraud, A, Kelly, G, Abramov, AY, Reilly, MM, Schiavo, G, Greensmith, L

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Débat loi Toubon

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police intervention at university campuses

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Clinical, pathological and functional characterization of riboflavin-responsive neuropathy von Manole, A, Jaunmuktane, Z, Hargreaves, I, Ludtmann, MHR, Salpietro, V, Bello, OD, Pope, S, Pandraud, A, Horga, A, Scalco, RS, Li, A, Ashokkumar, B, Lourenço, CM, Heales, S, Horvath, R, Chinnery, PF, Toro, C, Singleton, AB, Jacques, TS, Abramov, AY, Muntoni, F, Hanna, MG, Reilly, MM, Revesz, T, Kullmann, DM, Jepson, JEC, Houlden, H

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Football et politique

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