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Publisher: Springer Science and Media

Volume 263, Number 7, 2016

Multiple sclerosis in men: management considerations
pp. 1263-1273(11)
Authors: Bove, R.; McHenry, A.; Hellwig, K.; Houtchens, M.; Razaz, N.; Smyth, P.; Tremlett, H.; Sadovnick, A. D.; Rintell, D.

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Analysis of nocebo effects of antiepileptic drugs across different conditions
pp. 1274-1279(6)
Authors: Zaccara, G.; Giovannelli, F.; Giorgi, F. S.; Franco, V.; Gasparini, S.

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Traumatic brain injury and age at onset of cognitive impairment in older adults
pp. 1280-1285(6)
Authors: Li, W.; Risacher, S. L.; McAllister, T. W.; Saykin, A. J.

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Erratum to: Traumatic brain injury and age at onset of cognitive impairment in older adults
pp. 1286-1286(1)
Authors: Li, W.; Risacher, S. L.; McAllister, T. W.; Saykin, A. J.

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Activity of secukinumab, an anti-IL-17A antibody, on brain lesions in RRMS: results from a randomized, proof-of-concept study
pp. 1287-1295(9)
Authors: Havrdová, E.; Belova, A.; Goloborodko, A.; Tisserant, A.; Wright, A.; Wallstroem, E.; Garren, H.; Maguire, R. P.; Johns, D. R.

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The diagnostic value of biexponential apparent diffusion coefficients in myopathy
pp. 1296-1302(7)
Authors: Ran, J.; Liu, Y.; Sun, D.; Morelli, J.; Zhang, P.; Wu, G.; Sheng, Y.; Xie, R.; Zhang, X.; Li, X.

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Independent impact of infections on the course and outcome of status epilepticus: a 10-year cohort study
pp. 1303-1313(11)
Authors: Semmlack, S.; Tschudin-Sutter, S.; Widmer, A. F.; Valença, M.; Rüegg, S.; Marsch, S.; Sutter, R.

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Validation of a clinical practice-based algorithm for the diagnosis of autosomal recessive cerebellar ataxias based on NGS identified cases
pp. 1314-1322(9)
Authors: Mallaret, M.; Renaud, M.; Redin, C.; Drouot, N.; Muller, J.; Severac, F.; Mandel, J. L.; Hamza, W.; Benhassine, T.; Ali-Pacha, L.

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Timing of retinal neuronal and axonal loss in MS: a longitudinal OCT study
pp. 1323-1331(9)
Authors: Balk, L. J.; Cruz-Herranz, A. s.; Albrecht, P.; Arnow, S.; Gelfand, J. M.; Tewarie, P.; Killestein, J.; Uitdehaag, B. M.; Petzold, A.; Green, A. J.

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The association between white-matter tract abnormalities, and neuropsychiatric and cognitive symptoms in retired professional football players with multiple concussions
pp. 1332-1341(10)
Authors: Multani, N.; Goswami, R.; Khodadadi, M.; Ebraheem, A.; Davis, K. D.; Tator, C. H.; Wennberg, R.; Mikulis, D. J.; Ezerins, L.; Tartaglia, M. C.

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Erratum to: The association between white-matter tract abnormalities, and neuropsychiatric and cognitive symptoms in retired professional football players with multiple concussions
pp. 1342-1342(1)
Authors: Multani, N.; Goswami, R.; Khodadadi, M.; Ebraheem, A.; Davis, K. D.; Tator, C. H.; Wennberg, R.; Mikulis, D. J.; Ezerins, L.; Tartaglia, M. C.

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Subclinical primary retinal pathology in neuromyelitis optica spectrum disorder
pp. 1343-1348(6)
Authors: Jeong, I. H.; Kim, H. J.; Kim, N. H.; Jeong, K. S.; Park, C. Y.

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Clinical spectrum associated with MOG autoimmunity in adults: significance of sharing rodent MOG epitopes
pp. 1349-1360(12)
Authors: Sepúlveda, M.; Armangue, T. s.; Martinez-Hernandez, E.; Arrambide, G.; Sola-Valls, N.; Sabater, L.; Téllez, N.; Midaglia, L.; Ariño, H.; Peschl, P.

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Two cases of relapses in primary progressive multiple sclerosis after fingolimod withdrawal
pp. 1361-1363(3)
Authors: Davion, J. B.; Cambron, M.; Duhin, E.; Chouraki, A.; Lacour, A.; Labauge, P.; Carra, C.; Ayrignac, X.; Vermersch, P.

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Reliable volumetry of the cervical spinal cord in MS patient follow-up data with cord image analyzer (Cordial)
pp. 1364-1374(11)
Authors: Amann, M.; Pezold, S.; Naegelin, Y.; Fundana, K.; Andělová, M.; Weier, K.; Stippich, C.; Kappos, L.; Radue, E. W.; Cattin, P.

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Variants of windmill nystagmus
pp. 1375-1381(7)
Authors: Choi, K. D.; Shin, H. K.; Kim, J. S.; Kim, S. H.; Choi, J. H.; Kim, H. J.; Zee, D. S.

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Optic neuritis: a 5-year follow-up study of Chinese patients based on aquaporin-4 antibody status and ages
pp. 1382-1389(8)
Authors: Zhou, H.; Zhao, S.; Yin, D.; Chen, X.; Xu, Q.; Chen, T.; Li, X.; Wang, J.; Li, H.; Peng, C.

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A double-blind, randomized, cross-over, placebo-controlled, pilot trial with Sativex in Huntington’s disease
pp. 1390-1400(11)
Authors: López-Sendón Moreno, J. L.; García Caldentey, J.; Trigo Cubillo, P.; Ruiz Romero, C.; García Ribas, G.; Alonso Arias, M. A.; García de Yébenes, M. a.; Tolón, R. M.; Galve-Roperh, I.; Sagredo, O.

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Design, set-up and utility of the UK facioscapulohumeral muscular dystrophy patient registry
pp. 1401-1408(8)
Authors: Evangelista, T.; Wood, L.; Fernandez-Torron, R.; Williams, M.; Smith, D.; Lunt, P.; Hudson, J.; Norwood, F.; Orrell, R.; Willis, T.

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The interrelationship between disease severity, dynamic stability, and falls in cerebellar ataxia
pp. 1409-1417(9)
Authors: Schniepp, R.; Schlick, C.; Pradhan, C.; Dieterich, M.; Brandt, T.; Jahn, K.; Wuehr, M.

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Incidence and course of depression in multiple sclerosis in the multinational BEYOND trial
pp. 1418-1426(9)
Authors: Schippling, S.; O’Connor, P.; Knappertz, V.; Pohl, C.; Bogumil, T.; Suarez, G.; Cook, S.; Filippi, M.; Hartung, H. P.; Comi, G.

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A novel MYH2 mutation in family members presenting with congenital myopathy, ophthalmoplegia and facial weakness
pp. 1427-1433(7)
Authors: Willis, T.; Hedberg-Oldfors, C.; Alhaswani, Z.; Kulshrestha, R.; Sewry, C.; Oldfors, A.

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Efficacy of focal mechanic vibration treatment on balance in Charcot-Marie-Tooth 1A disease: a pilot study
pp. 1434-1441(8)
Authors: Pazzaglia, C.; Camerota, F.; Germanotta, M.; Sipio, E.; Celletti, C.; Padua, L.

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Multiple sclerosis and chronic progressive external ophthalmoplegia associated with a large scale mitochondrial DNA single deletion
pp. 1449-1451(3)
Authors: Gaetani, L.; Mignarri, A.; Di Gregorio, M.; Sarchielli, P.; Malandrini, A.; Cardaioli, E.; Calabresi, P.; Dotti, M. T.; Di Filippo, M.

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Phenotypic spectrum of the m.8344A>G mutation
pp. 1452-1453(2)
Authors: Finsterer, J.; Zarrouk-Mahjoub, S.

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EGR2 mutation enhances phenotype spectrum of Dejerine–Sottas syndrome
pp. 1456-1458(3)
Authors: Gargaun, E.; Seferian, A. M.; Cardas, R.; Moing, A. G.; Delanoe, C.; Nectoux, J.; Nelson, I.; Bonne, G. l.; Bihoreau, M. T.; Deleuze, J. F.

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Letter to the editor: confirming neonatal seizure and late onset ataxia in SCN2A Ala263Val
pp. 1459-1460(2)
Authors: Johannesen, K. M.; Miranda, M. J.; Lerche, H.; Møller, R. S.

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Evolving neuromuscular phenotype in a patient with a heterozygous CHCHD10 p.G66V mutation
pp. 1461-1462(2)
Authors: Jokela, M. E.; Joutsa, J.; Udd, B.

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Dementia and assisted suicide and euthanasia
pp. 1463-1467(5)
Authors: Beaufort, I. D.; Vathorst, S.

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Jules Tinel (1879–1952)
pp. 1471-1472(2)
Authors: Pietrzak, K.; Grzybowski, A.; Kaczmarczyk, J.

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