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42.
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Spinal Stenosis in Familial Transthyretin Amyloidosis. [electronic resource] by
- Carr, A S
- Shah, S
- Choi, D
- Blake, J
- Phadke, R
- Gilbertson, J
- Whelan, C J
- Wechalekar, A D
- Gillmore, J D
- Hawkins, P N
- Reilly, M M
Producer: 20191216
In:
Journal of neuromuscular diseases vol. 6
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43.
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Routine blood monitoring in maintenance immunoglobulin treatment of inflammatory neuropathy: Is it clinically relevant? [electronic resource] by
- Keh, R
- Kahlil, A
- Nihoyannopoulos, L
- Compton, L
- Kapoor, M
- Gosal, D
- Manji, H
- Rossor, A M
- Reilly, M M
- Lunn, M P
- Lavin, T M
- Carr, A S
Producer: 20210319
In:
Journal of the neurological sciences vol. 408
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44.
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MRI shows increased sciatic nerve cross sectional area in inherited and inflammatory neuropathies. [electronic resource] by
- Sinclair, C D J
- Miranda, M A
- Cowley, P
- Morrow, J M
- Davagnanam, I
- Mehta, H
- Hanna, M G
- Koltzenburg, M
- Reilly, M M
- Yousry, T A
- Thornton, J S
Producer: 20111213
In:
Journal of neurology, neurosurgery, and psychiatry vol. 82
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45.
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Skeletal muscle MRI magnetisation transfer ratio reflects clinical severity in peripheral neuropathies. [electronic resource] by
- Sinclair, C D J
- Morrow, J M
- Miranda, M A
- Davagnanam, I
- Cowley, P C
- Mehta, H
- Hanna, M G
- Koltzenburg, M
- Yousry, T A
- Reilly, M M
- Thornton, J S
Producer: 20120202
In:
Journal of neurology, neurosurgery, and psychiatry vol. 83
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46.
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Alemtuzumab in the treatment of IVIG-dependent chronic inflammatory demyelinating polyneuropathy. [electronic resource] by
- Marsh, E A
- Hirst, C L
- Llewelyn, J G
- Cossburn, M D
- Reilly, M M
- Krishnan, A
- Doran, M
- Ryan, A M
- Coles, A J
- Jones, J L
- Robertson, N P
Producer: 20100929
In:
Journal of neurology vol. 257
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47.
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Variable phenotypes are associated with PMP22 missense mutations. [electronic resource] by
- Russo, M
- Laurá, M
- Polke, J M
- Davis, M B
- Blake, J
- Brandner, S
- Hughes, R A C
- Houlden, H
- Bennett, D L H
- Lunn, M P T
- Reilly, M M
Producer: 20110421
In:
Neuromuscular disorders : NMD vol. 21
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48.
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GJB1 gene mutations in suspected inflammatory demyelinating neuropathies not responding to treatment. [electronic resource] by
- Michell, A W
- Laura, M
- Blake, J
- Lunn, M P
- Cox, A
- Gibbons, V S
- Davis, M B
- Wood, N W
- Manji, H
- Houlden, H
- Murray, N M F
- Reilly, M M
Producer: 20090601
In:
Journal of neurology, neurosurgery, and psychiatry vol. 80
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49.
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A study of the neuropathy associated with transthyretin amyloidosis (ATTR) in the UK. [electronic resource] by
- Carr, A S
- Pelayo-Negro, A L
- Evans, M Rb
- Laurà, M
- Blake, J
- Stancanelli, C
- Iodice, V
- Wechalekar, A D
- Whelan, C J
- Gillmore, J D
- Hawkins, P N
- Reilly, M M
Producer: 20170529
In:
Journal of neurology, neurosurgery, and psychiatry vol. 87
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50.
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Nerve conduction velocity in CMT1A: what else can we tell? [electronic resource] by
- Manganelli, F
- Pisciotta, C
- Reilly, M M
- Tozza, S
- Schenone, A
- Fabrizi, G M
- Cavallaro, T
- Vita, G
- Padua, L
- Gemignani, F
- Laurà, M
- Hughes, R A C
- Solari, A
- Pareyson, D
- Santoro, L
Producer: 20171219
In:
European journal of neurology vol. 23
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51.
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Recessive axonal Charcot-Marie-Tooth disease due to compound heterozygous mitofusin 2 mutations. [electronic resource] 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
Producer: 20110909
In:
Neurology vol. 77
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52.
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Is overwork weakness relevant in Charcot-Marie-Tooth disease? [electronic resource] by
- Piscosquito, G
- Reilly, M M
- Schenone, A
- Fabrizi, G M
- Cavallaro, T
- Santoro, L
- Vita, G
- Quattrone, A
- Padua, L
- Gemignani, F
- Visioli, F
- Laurà, M
- Calabrese, D
- Hughes, R A C
- Radice, D
- Solari, A
- Pareyson, D
Producer: 20150206
In:
Journal of neurology, neurosurgery, and psychiatry vol. 85
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53.
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Altered TDP-43-dependent splicing in HSPB8-related distal hereditary motor neuropathy and myofibrillar myopathy. [electronic resource] by
- Cortese, A
- Laurà, M
- Casali, C
- Nishino, I
- Hayashi, Y K
- Magri, S
- Taroni, F
- Stuani, C
- Saveri, P
- Moggio, M
- Ripolone, M
- Prelle, A
- Pisciotta, C
- Sagnelli, A
- Pichiecchio, A
- Reilly, M M
- Buratti, E
- Pareyson, D
Producer: 20181119
In:
European journal of neurology vol. 25
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54.
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Responsiveness of clinical outcome measures in Charcot-Marie-Tooth disease. [electronic resource] by
- Piscosquito, G
- Reilly, M M
- Schenone, A
- Fabrizi, G M
- Cavallaro, T
- Santoro, L
- Manganelli, F
- Vita, G
- Quattrone, A
- Padua, L
- Gemignani, F
- Visioli, F
- Laurà, M
- Calabrese, D
- Hughes, R A C
- Radice, D
- Solari, A
- Pareyson, D
Producer: 20160617
In:
European journal of neurology vol. 22
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55.
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Transthyretin V122I amyloidosis with clinical and histological evidence of amyloid neuropathy and myopathy. [electronic resource] by
- Carr, A S
- Pelayo-Negro, A L
- Jaunmuktane, Z
- Scalco, R S
- Hutt, D
- Evans, M R B
- Heally, E
- Brandner, S
- Holton, J
- Blake, J
- Whelan, C J
- Wechalekar, A D
- Gillmore, J D
- Hawkins, P N
- Reilly, M M
Producer: 20160217
In:
Neuromuscular disorders : NMD vol. 25
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56.
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Mutations in the tail domain of DYNC1H1 cause dominant spinal muscular atrophy. [electronic resource] 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
Producer: 20120730
In:
Neurology vol. 78
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57.
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Oculoleptomeningeal Amyloidosis associated with transthyretin Leu12Pro in an African patient. [electronic resource] by
- 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
Producer: 20160404
In:
Journal of neurology vol. 262
Availability: No items available.
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58.
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Frequency of mutations in the genes associated with hereditary sensory and autonomic neuropathy in a UK cohort. [electronic resource] by
- 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
Producer: 20130604
In:
Journal of neurology vol. 259
Availability: No items available.
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59.
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CMT subtypes and disease burden in patients enrolled in the Inherited Neuropathies Consortium natural history study: a cross-sectional analysis. [electronic resource] by
- 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
Producer: 20150930
In:
Journal of neurology, neurosurgery, and psychiatry vol. 86
Availability: No items available.
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