Trigeminal neuralgia associated with osteogenesis imperfecta.

od Reilly, M M, Valentine, A R, Ginsberg, L
Wydane 1995

Familial amyloid polyneuropathy (TTR ala 60) in north west Ireland: a clinical, genetic, and epidemiological study.

od Reilly, M M, Staunton, H, Harding, A E
Wydane 1995

Vitamin C and Charcot–Marie–Tooth 1A: Pharmacokinetic considerations

od Visioli, F., Reilly, M.M., Rimoldi, M., Solari, A., Pareyson, D.
Wydane 2013

A novel amyloidogenic transthyretin variant, Gly53Ala, associated with intermittent headaches and ataxia

od Douglass, C, Suvarna, K, Reilly, M M, Hawkins, P N, Hadjivassiliou, M
Wydane 2007

Treatment of chronic inflammatory demyelinating polyradiculoneuropathy with methotrexate

od Fialho, D, Chan, Y‐C, Allen, D C, Reilly, M M, Hughes, R A C
Wydane 2006

MFN2 mutations cause severe phenotypes in most patients with CMT2A

od Feely, S.M.E., Laura, M., Siskind, C.E., Sottile, S., Davis, M., Gibbons, V.S., Reilly, M.M., Shy, M.E.
Wydane 2011

The use of nerve and muscle biopsy in the diagnosis of vasculitis: a 5 year retrospective study

od Bennett, D L H, Groves, M, Blake, J, Holton, J L, King, R H M, Orrell, R W, Ginsberg, L, Reilly, M M
Wydane 2008

Hand weakness in Charcot-Marie-Tooth disease 1X

od Arthur-Farraj, P.J., Murphy, S.M., Laura, M., Lunn, M.P., Manji, H., Blake, J., Ramdharry, G., Fox, Z., Reilly, M.M.
Wydane 2012

Primary sciatic nerve lymphoma: a case report and review of the literature

od Descamps, M J L, Barrett, L, Groves, M, Yung, L, Birch, R, Murray, N M F, Linch, D C, Lunn, M P T, Reilly, M M
Wydane 2006

Clinical spectrum, treatment and outcome of children with suspected diagnosis of chronic inflammatory demyelinating polyradiculoneuropathy

od 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.
Wydane w Neuromuscul Disord (2018)

Recessive axonal Charcot-Marie-Tooth disease due to compound heterozygous mitofusin 2 mutations

od 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.
Wydane 2011

Mutations in the tail domain of DYNC1H1 cause dominant spinal muscular atrophy

od 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.
Wydane 2012

Oculoleptomeningeal Amyloidosis associated with transthyretin Leu12Pro in an African patient

od McColgan, P., Viegas, S., Gandhi, S., Bull, K., Tudor, R., Sheikh, F., Pinney, J., Fontana, M., Rowczenio, D., Gillmore, J. D., Gilbertson, J. A., Whelan, C. J., Shah, S., Jaunmuktane, Z., Holton, J. L., Schott, J. M., Werring, D. J., Hawkins, P. N., Reilly, M. M.
Wydane w J Neurol (2014)

Frequency of mutations in the genes associated with hereditary sensory and autonomic neuropathy in a UK cohort

od Davidson, G. L., Murphy, S. M., Polke, J. M., Laura, M., Salih, M. A. M., Muntoni, F., Blake, J., Brandner, S., Davies, N., Horvath, R., Price, S., Donaghy, M., Roberts, M., Foulds, N., Ramdharry, G., Soler, D., Lunn, M. P., Manji, H., Davis, M. B., Houlden, H., Reilly, M. M.
Wydane 2012

CMT subtypes and disease burden in patients enrolled in the Inherited Neuropathies Consortium natural history study: a cross-sectional analysis

od Fridman, V, Bundy, B, Reilly, M M, Pareyson, D, Bacon, C, Burns, J, Day, J, Feely, S, Finkel, R S, Grider, T, Kirk, C A, Herrmann, D N, Laurá, M, Li, J, Lloyd, T, Sumner, C J, Muntoni, F, Piscosquito, G, Ramchandren, S, Shy, R, Siskind, C E, Yum, S W, Moroni, I, Pagliano, E, Zuchner, S, Scherer, S S, Shy, M E
Wydane w J Neurol Neurosurg Psychiatry (2015)