In This Issue
Editorials
Articles
- Rates of global and regional cerebral atrophy in AD and frontotemporal dementiaD. Chan, N. C. Fox, R. Jenkins, R. I. Scahill, W. R. Crum, M. N. Rossor
- The cerebrospinal fluid production rate is reduced in dementia of the Alzheimer’s typeG.D. Silverberg, G. Heit, S. Huhn, R.A. Jaffe, S.D. Chang, H. Bronte–Stewart, E. Rubenstein, K. Possin, T.A. Saul
- Optical filters inhibiting television-induced photosensitive seizuresY. Takahashi, T. Sato, K. Goto, M. Fujino, T. Fujiwara, M. Yamaga, H. Isono, N. Kondo
- Randomized controlled trial of zonisamide for the treatment of refractory partial-onset seizuresE. Faught, R. Ayala, G. G. Montouris, I. E. Leppik, the Zonisamide 922 Trial Group
- Individual state driving restrictions for people with epilepsy in the USGregory L. Krauss, Lorraine Ampaw, Allan Krumholz
- Memory fMRI lateralizes temporal lobe epilepsyHennric Jokeit, Michael Okujava, Friedrich G. Woermann
- Hyperexcitable cortical responses in progressive myoclonic epilepsyA TMS studyP. Manganotti, S. Tamburin, G. Zanette, A. Fiaschi
- Seizures in family members of patients with hippocampal sclerosisRegula S. Briellmann, Yvonne Torn–Broers, Graeme D. Jackson, Samuel F. Berkovic
- Ischemic stroke and active migraineDidier Milhaud, Julien Bogousslavsky, Guy van Melle, Pierre Liot
- Dose finding, placebo-controlled study of oral almotriptan in the acute treatment of migraineC. Dahlöf, P. Tfelt–Hansen, H. Massiou, A. Fazekas
- Experimental brush-evoked allodynia activates posterior parietal cortexN. Witting, R. C. Kupers, P. Svensson, L. Arendt–Nielsen, A. Gjedde, T. S. Jensen
- Prospective follow-up of 33 asymptomatic patients with familial cerebral cavernous malformationsP. Labauge, L. Brunereau, S. Laberge, J.-P. Houtteville
- Serotonin 5-HT1A agonist improves motor complications in rodent and primate parkinsonian modelsFrancesco Bibbiani, Justin D. Oh, Thomas N. Chase
- Interactions between deep brain stimulation and levodopa in Parkinson’s diseaseJ.G. Nutt, S.L. Rufener, J.H. Carter, V.C. Anderson, R. Pahwa, J.P. Hammerstad, K.J. Burchiel
- Loss-of-function EA2 mutations are associated with impaired neuromuscular transmissionJ. Jen, J. Wan, M. Graves, H. Yu, A. F. Mock, C. J. Coulin, G. Kim, Q. Yue, D. M. Papazian, R. W. Baloh
- Gating of myotonic Na channel mutants defines the response to mexiletine and a potent derivativeJ.-F. Desaphy, A. De Luca, P. Tortorella, D. De Vito, A. L. George, D. Conte Camerino
- Effect of neurophilin ligands on motor units in mice with SOD1 ALS mutationsJ. M. Shefner, R. H. Brown, D. Cole, P. Chaturvedi, D. Schoenfeld, K. Pastuszak, R. Matthews, M. Upton–Rice, M. E. Cudkowicz
- Cerebellar mediation of the complexity of bimanual compared to unimanual movementsJ. I. Tracy, S. S. Faro, F. B. Mohammed, A. B. Pinus, S. M. Madi, J. W. Laskas
- Interferon-β1b in the treatment of secondary progressive MSImpact on quality of lifeJ. A. Freeman, A. J. Thompson, R. Fitzpatrick, M. Hutchinson, C. Miltenburger, K. Beckmann, F. Dahlke, L. Kappos, C. Polman, C. Pozzilli, the European Study Group on Interferon-β1b in Secondary Progressive MS
- Surgical therapy for tremor in multiple sclerosisAn evaluation of outcome measuresJ. Matsumoto, D. Morrow, K. Kaufman, D. Davis, J.E. Ahlskog, A. Walker, D. Sneve, J. Noseworthy, M. Rodriguez
Views & Reviews
- The genetic epidemiology of gliomaR. H. Osborne, M. P.W.A. Houben, C. C. Tijssen, J. W.W. Coebergh, C. M. van Duijn
Clinical/Scientific Notes
- Optimization of the single-day praziquantel therapy for neurocysticercosisM. López–Gómez, N. Castro, H. Jung, J. Sotelo, T. Corona
- A mutation in mt tRNALeu(UUR) causing a neuropsychiatric syndrome with depression and cataractM. Jaksch, H. Lochmuller, F. Schmitt, B. Volpel, B. Obermaier–Kusser, R. Horvath
- Reinduction of hyponatremia to treat central pontine myelinolysisSoichi Oya, Kazuo Tsutsumi, Keisuke Ueki, Takaaki Kirino
- Possible efficacy of temozolomide in a patient with gliomatosis cerebriAli Benjelloun, Jacqueline Delavelle, François Lazeyras, Pierre-Yves Dietrich
- Hyperperfusion-induced intracerebral hemorrhage after carotid stenting documented by TCDT. Pfefferkorn, T. Mayer, S. Von Stuckrad–Barre, M. Covi, G. F. Hamann
NeuroImages
- Miller Fisher syndrome: MRI findingsC. A. Garcia–Rivera, T.D. Rozen, D. Zhou, P. Allahyari, R. Niknam, D. Dougherty, J. Morgan, A. Flanders
Correspondence
- Juvenile and adult-onset acid maltase deficiency in France: Genotype–phenotype correlationM.G. E. M. Ausems, J.H. J. Wokke, A.J.J. Reuser, O.P. van Diggelen
- Evidence for neuroaxonal injury in patients with proteolipid gene mutationsJ. Garbern, M. Shy, K. Krajewski, J. Kamholz, G. Hobson, F. Cambi
- Quality of life in ALS is maintained as physical function declinesF. Maillot, L. Laueriere, E. Hazouard, B. Giraudeau, P. Corcia
- Neuropsychological assessment in children with absence epilepsyGabriel M. Ronen, Brandon F. Meaney, Charles Cunningham
Calendar
Filler
Brief Communications
- Sample size estimations for MRI-monitored trials of MS comparing new vs standard treatmentsM. P. Sormani, M. Rovaris, F. Bagnato, P. Molyneux, P. Bruzzi, C. Pozzilli, D. H. Miller, G. Comi, M. Filippi
- Onset of multiple sclerosis associated with anti-TNF therapyNancy L. Sicotte, Rhonda R. Voskuhl
- Transcallosal bands: A sign of neuronal tract degeneration in early MS?Jack H. Simon, Lawrence Jacobs, R. Philip Kinkel
- High incidence and increasing prevalence of MS in Enna (Sicily), southern ItalyL. M.E. Grimaldi, G. Salemi, G. Grimaldi, A. Rizzo, R. Marziolo, C. Lo Presti, D. Maimone, G. Savettieri
- Polymorphisms in the vicinity of the hypocretin/orexin are not associated with human narcolepsyMarcel Hungs, Ling Lin, Michele Okun, Emmanuel Mignot
- Polymorphisms in hypocretin/orexin pathway genes and narcolepsyB. R. Ólafsdóttir, D. B. Rye, T. E. Scammell, J. K. Matheson, K. Stefánsson, J. R. Gulcher
- Sustained excitability elevations induced by transcranial DC motor cortex stimulation in humansMichael A. Nitsche, Walter Paulus
- Catastrophic reaction in acute stroke: A reflex behavior in aphasic patientsAntonio Carota, Andrea O. Rossetti, Theodoros Karapanayiotides, Julien Bogousslavsky
- Episodes of generalized weakness in two sibs with the C164T mutation of the connexin 32 geneMarios Panas, Nikolaos Kalfakis, Charalampos Karadimas, Demetris Vassilopoulos
- Antiganglioside antibodies in polyneuropathy associated with monoclonal gammopathyM. Eurelings, C. W. Ang, N. C. Notermans, P. A. Van Doorn, B. C. Jacobs, L. H. Van den Berg
- A new autosomal dominant pure cerebellar ataxiaE. Storey, R. J.M. Gardner, M. A. Knight, M. L. Kennerson, R. R. Tuck, S. M. Forrest, G. A. Nicholson
- No reversion in vigabatrin-associated visual field defectsIiris Nousiainen, Maija Mäntyjärvi, Reetta Kälviäinen
- The efficacy of epidural blood patch in spontaneous CSF leaksDrahomira Sencakova, Bahram Mokri, Robyn L. McClelland
- Apolipoprotein E and age at onset of Alzheimer’s disease in African American patientsF.C. Goldstein, A.V. Ashley, M. Gearing, J. Hanfelt, L. Penix, L.J. Freedman, A.I. Levey
- A novel presenilin 2 gene mutation (D439A) in a patient with early-onset Alzheimer’s diseaseA. Lleó, R. Blesa, J. Gendre, M. Castellví, P. Pastor, R. Queralt, R. Oliva
Changes, People, Comments