检索结果 - Reilly, MM
- Showing 1 - 13 results of 13
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Recent advances in the genetic neuropathies 由 Rossor, AM, Tomaselli, PJ, Reilly, MM
出版 2016Text -
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A diagnostic conundrum 由 Keddie, S, Jaunmuktane, Z, Brandner, S, Shah, S, Maddison, P, Rees, JH, Hanna, MG, Lunn, MP, Reilly, MM, Rossor, AM, Carr, AS
出版 2018Text -
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Clinical spectrum, treatment and outcome of children with suspected diagnosis of chronic inflammatory demyelinating polyradiculoneuropathy 由 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.
出版 2018Text -
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Mutation in RNF170 causes sensory ataxic neuropathy with vestibular areflexia: a CANVAS mimic 由 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
出版 2020Text -
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Recessive axonal Charcot-Marie-Tooth disease due to compound heterozygous mitofusin 2 mutations 由 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.
出版 2011Text -
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Phenotypic variability of childhood Charcot-Marie-Tooth disease 由 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
出版 2016Text -
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Mutations in the tail domain of DYNC1H1 cause dominant spinal muscular atrophy 由 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.
出版 2012Text