In This Issue
Editorials
- What’s in the serum of seronegative MG and LEMS?MuSK et al.Angela Abicht, Hanns Lochmüller
- Sweetening the pot in muscleGenetic defects of protein glycosylation causing muscle diseaseGeorge Karpati, Paul Holland
Articles
- AChR phosphorylation and indirect inhibition of AChR function in seronegative MGC.P. Plested, T. Tang, I. Spreadbury, E.T. Littleton, U. Kishore, A. Vincent
- Distal myopathy with rimmed vacuoles is allelic to hereditary inclusion body myopathyI. Nishino, S. Noguchi, K. Murayama, A. Driss, K. Sugie, Y. Oya, T. Nagata, K. Chida, T. Takahashi, Y. Takusa, T. Ohi, J. Nishimiya, N. Sunohara, E. Ciafaloni, M. Kawai, M. Aoki, I. Nonaka
- A randomized, double-blind, placebo-controlled trial of a glycine antagonist in neuropathic painM. S. Wallace, M. C. Rowbotham, N. P. Katz, R. H. Dworkin, R. M. Dotson, B. S. Galer, R. L. Rauck, M. M. Backonja, S. N. Quessy, P. D. Meisner
- Migraine and Ménière’s diseaseIs there a link?A. Radtke, T. Lempert, M.A. Gresty, G.B. Brookes, A.M. Bronstein, H. Neuhauser
- Transient restless legs syndrome after spinal anesthesiaA prospective studyB. Högl, B. Frauscher, K. Seppi, H. Ulmer, W. Poewe
- The association of incident dementia with mortality in PDG. Levy, M.-X. Tang, E.D. Louis, L.J. Côté, B. Alfaro, H. Mejia, Y. Stern, K. Marder
- Fluctuations in attentionPD dementia vs DLB with parkinsonismC.G. Ballard, D. Aarsland, I. McKeith, J. O’Brien, A. Gray, F. Cormack, D. Burn, T. Cassidy, R. Starfeldt, J.-P. Larsen, R. Brown, M. Tovee
- The incremental direct costs associated with behavioral symptoms in ADD.L. Murman, Q. Chen, M.C. Powell, S.B. Kuo, C.J. Bradley, C.C. Colenda
- Prognosis for seizure recurrence in patients with newly diagnosed neurocysticercosisArturo Carpio, W. Allen Hauser
- Outcomes of 32 hemispherectomies for Sturge–Weber syndrome worldwideEric H. Kossoff, Carol Buck, John M. Freeman
- Kleine-Levin syndromeAn autoimmune hypothesis based on clinical and genetic analysesY. Dauvilliers, G. Mayer, M. Lecendreux, E. Neidhart, R. Peraita-Adrados, K. Sonka, M. Billiard, M. Tafti
- Biochemical markers predicting survival in peroxisome biogenesis disordersJ. Gootjes, P.A.W. Mooijer, C. Dekker, P.G. Barth, B.T. Poll-The, H.R. Waterham, R.J.A. Wanders
- Global and domain-specific cognitive impairment and outcome after subarachnoid hemorrhageS. A. Mayer, K. T. Kreiter, D. Copeland, G. L. Bernardini, J. E. Bates, S. Peery, J. Claassen, Y. E. Du, E. S. Connolly
- Evaluation of clinical diagnostic criteria for neurofibromatosis 2M. E. Baser, J. M. Friedman, A. J. Wallace, R. T. Ramsden, H. Joe, D. G.R. Evans
- Axonal damage in the spinal cord of MS patients occurs largely independent of T2 MRI lesionsE. Bergers, J.C.J. Bot, C.J.A. De Groot, C.H. Polman, G.J. Lycklama à Nijeholt, J.A. Castelijns, P. van der Valk, F. Barkhof
Views & Reviews
Clinical/Scientific Notes
- An Italian family with autosomal recessive inclusion-body myopathy and mutations in the GNE geneA. Broccolini, M. Pescatori, A. D’Amico, A. Sabino, G. Silvestri, E. Ricci, S. Servidei, P. A. Tonali, M. Mirabella
- Ethylene glycol intoxication: Electrophysiological studies suggest a polyradiculopathyL. Zhou, R. Zabad, R.A. Lewis
- Phrenic nerve paralysis secondary to Lyme neuroborreliosisSaliha Ishaq, Robert Quinet, Jihan Saba
- Meningoradiculitis associated with giant cell arteritisU. Roelcke, D. Eschle, L. Kappos, M. Moschopulos, R.H. Laeng, U.W. Buettner
- Lonely cowboy’s thoughtsCatherine Thomas Antérion, Sandrine Honoré-Masson, Stéphanie Dirson, Bernard Laurent
- A sequential bilateral medial medullary infarction separated by 4 monthsSo-Young Moon, Hahn-Young Kim, Chin-Sang Chung
- Epilepsia partialis continua as an atypical presentation of cat scratch disease in a young adultGrzegorz S. Nowakowski, Amiram Katz
- An autoantibody to GAD65 in sera of patients with juvenile neuronal ceroid lipofuscinosesSubrata Chattopadhyay, Elizabeth Kriscenski-Perry, David A. Wenger, David A. Pearce
NeuroImages
Correspondence
- Morbidity and mortality following pallidotomy in PDValérie Biousse, Nancy J. Newman
- Progressive bulbospinal amyotrophy in triple A syndrome with AAAS gene mutationMamede de Carvalho, Henry Houlden
- Chronic inflammatory demyelinating polyneuropathy presenting with features of GBSIsabelle Korn-Lubetzki, Israel Steiner
Departments
Brief Communications
- Seronegative Lambert-Eaton myasthenic syndromeStudy of 110 Japanese patientsY.K. Nakao, M. Motomura, T. Fukudome, T. Fukuda, H. Shiraishi, T. Yoshimura, M. Tsujihata, K. Eguchi
- GNE mutations in an American family with quadriceps-sparing IBM and lack of mutations in s-IBMOlavo M. Vasconcelos, Raghavan Raju, Marinos C. Dalakas
- Diagnostic criteria for dystonia in DYT1 familiesS. B. Bressman, D. Raymond, K. Wendt, R. Saunders–Pullman, D. de Leon, S. Fahn, L. Ozelius, N. Risch
- Exon deletions in the GCHI gene in two of four Turkish families with dopa-responsive dystoniaC. Klein, K. Hedrich, K. Kabakçi, K. Mohrmann, K. Wiegers, O. Landt, J. Hagenah, E. Schwinger, P. P. Pramstaller, L. J. Ozelius, K. Gucuyener, S. Aysun, E. Demir
- Driving safety in Parkinson’s diseaseT. A. Zesiewicz, C. R. Cimino, A. R. Malek, N. Gardner, P. L. Leaverton, P. B. Dunne, R. A. Hauser
- Repetitive transcranial magnetic stimulation for Tourette syndromeA. Münchau, B.R. Bloem, K.V. Thilo, M.R. Trimble, J.C. Rothwell, M.M. Robertson
- Clinical and genetic studies of families with the tau N279K mutation (FTDP-17)Y. Tsuboi, M. Baker, M. L. Hutton, R. J. Uitti, O. Rascol, M.-B. Delisle, X. Soulages, J. R. Murrell, B. Ghetti, M. Yasuda, O. Komure, S. Kuno, K. Arima, N. Sunohara, T. Kobayashi, Y. Mizuno, Z. K. Wszolek
- Higher attack rates for left motor deficit among men with cerebrovascular eventsD. Devroey, F. Buntinx, V. Van Castere, J. Van Der Heyden, H. Vandenberghe
- Carotid artery dissection after the intracarotid amobarbital testTobias Loddenkemper, Harold H. Morris, John Perl
- Impaired renal function in progressive multiple sclerosisP.A. Calabresi, H. Austin, M.K. Racke, A. Goodman, P. Choyke, H. Maloni, H.F. McFarland
- Adult onset glutaric aciduria type I presenting with a leukoencephalopathyO. Bähr, I. Mader, J. Zschocke, J. Dichgans, J.B. Schulz
- Identification of a susceptibility locus for migraine with and without aura on 6p12.2-p21.1A. Carlsson, L. Forsgren, P.-O. Nylander, U. Hellman, K. Forsman-Semb, G. Holmgren, D. Holmberg, M. Holmberg
Nisus: Neurology and the Humanities
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