Search Results - Reilly, MM

Recent advances in the genetic neuropathies by Rossor, AM, Tomaselli, PJ, Reilly, MM

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Are we prepared for clinical trials in Charcot-Marie-Tooth disease? by Rossor, AM, Shy, ME, Reilly, MM

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Vitamin C and Charcot–Marie–Tooth 1A: Pharmacokinetic considerations by Visioli, F., Reilly, M.M., Rimoldi, M., Solari, A., Pareyson, D.

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A diagnostic conundrum by Keddie, S, Jaunmuktane, Z, Brandner, S, Shah, S, Maddison, P, Rees, JH, Hanna, MG, Lunn, MP, Reilly, MM, Rossor, AM, Carr, AS

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A STUDY OF PHYSICAL ACTIVITY COMPARING PEOPLE WITH CHARCOT-MARIE-TOOTH DISEASE TO NORMAL CONTROL SUBJECTS by Ramdharry, GM, Pollard, AJ, Grant, R, Dewar, EL, Laura, M, Moore, SA, Hallsworth, K, Ploetz, T, Trenell, MI, Reilly, MM

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MFN2 mutations cause severe phenotypes in most patients with CMT2A by Feely, S.M.E., Laura, M., Siskind, C.E., Sottile, S., Davis, M., Gibbons, V.S., Reilly, M.M., Shy, M.E.

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Hand weakness in Charcot-Marie-Tooth disease 1X by Arthur-Farraj, P.J., Murphy, S.M., Laura, M., Lunn, M.P., Manji, H., Blake, J., Ramdharry, G., Fox, Z., Reilly, M.M.

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Clinical spectrum, treatment and outcome of children with suspected diagnosis of chronic inflammatory demyelinating polyradiculoneuropathy by Silwal, A., Pitt, M., Phadke, R., Mankad, K., Davison, J.E., Rossor, A., DeVile, C., Reilly, M.M., Manzur, A.Y., Muntoni, F., Munot, P.

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NERVE CONDUCTION VELOCITY IN CMT1A: WHAT ELSE CAN WE TELL by Manganelli, F, Pisciotta, C, Reilly, MM, Tozza, S, Schenone, A, Fabrizi, GM, Cavallaro, T, Vita, G, Padua, L, Gemignani, F, Laura, M, Hughes, RAC, Solari, A, Pareyson, D, Santoro, L

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Mutation in RNF170 causes sensory ataxic neuropathy with vestibular areflexia: a CANVAS mimic by Cortese, A, Callegari, I., Curro, R., Vegezzi, E., Colnaghi, S., Versino, M., Alfonsi, E., Cosentino, G., Valente, EM., Gana, S., Tassorelli, C., Pichiecchio, A, Rossor, AM., Bugiardini, E., Biroli, A., Di Capua, D., Houlden, H., Reilly, MM

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Recessive axonal Charcot-Marie-Tooth disease due to compound heterozygous mitofusin 2 mutations by Polke, J.M., Laurá, M., Pareyson, D., Taroni, F., Milani, M., Bergamin, G., Gibbons, V.S., Houlden, H., Chamley, S.C., Blake, J., DeVile, C., Sandford, R., Sweeney, M.G., Davis, M.B., Reilly, M.M.

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Phenotypic variability of childhood Charcot-Marie-Tooth disease by Cornett, KMD, Menezes, MP, Bray, P, Halaki, M, Shy, R, Yum, SW, Estilow, T, Moroni, I, Foscan, M, Pagliano, E, Pareyson, D, Laura, M, Bandhari, T, Muntoni, F, Reilly, MM, Finkel, RS, Sowden, J, Eichinger, K, Herrmann, DN, Shy, ME, Burns, J

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Mutations in the tail domain of DYNC1H1 cause dominant spinal muscular atrophy by Harms, M.B., Ori-McKenney, K.M., Scoto, M., Tuck, E.P., Bell, S., Ma, D., Masi, S., Allred, P., Al-Lozi, M., Reilly, M.M., Miller, L.J., Jani-Acsadi, A., Pestronk, A., Shy, M.E., Muntoni, F., Vallee, R.B., Baloh, R.H.

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