In This Issue
Editorials
- Face module, face networkThe cognitive architecture of the brain revealed through studies of face processingAnjan Chatterjee, Martha J. Farah
- Genetic association studiesGenes in search of diseasesThomas D. Bird, Gail P. Jarvik, Nicholas W. Wood
Articles
- Covert recognition in acquired and developmental prosopagnosiaJason J.S. Barton, Mariya Cherkasova, Margaret O’Connor
- Face memory impairments in patients with frontal lobe damageS. Z. Rapcsak, L. Nielsen, L. D. Littrell, E. L. Glisky, A. W. Kaszniak, J. F. Laguna
- Serial EEG during human status epilepticusEvidence for PLED as an ictal patternEliana Garzon, Regina Maria França Fernandes, Américo Ceiki Sakamoto
- In vivo hippocampal glucose metabolism in mesial temporal lobe epilepsyR. C. Knowlton, K. D. Laxer, G. Klein, S. Sawrie, G. Ende, R. A. Hawkins, O. S. Aassar, K. Soohoo, S. Wong, N. Barbaro
- Generalized epilepsy with febrile seizures plusFurther heterogeneity in a large familyH. Lerche, Y. G. Weber, H. Baier, K. Jurkat–Rott, O. Kraus de Camargo, A. C. Ludolph, H. Bode, F. Lehmann–Horn
- The Clomethiazole Acute Stroke Study in tissue-type plasminogen activator–treated stroke (CLASS-T)Final resultsP. Lyden, M. Jacoby, J. Schim, G. Albers, P. Mazzeo, T. Ashwood, A. Nordlund, T. Odergren, the CLASS IHT Investigators*
- Relationship between severity of MR perfusion deficit and DWI lesion evolutionV. N. Thijs, A. Adami, T. Neumann–Haefelin, M. E. Moseley, M. P. Marks, G. W. Albers
- Small cerebral aneurysms presenting with symptoms other than ruptureJ. A. Friedman, D. G. Piepgras, M. A. Pichelmann, K. K. Hansen, R. D. Brown, D. O. Wiebers
- Poststroke dementiaIncidence and relationship to prestroke cognitive declineH. Hénon, I. Durieu, D. Guerouaou, F. Lebert, F. Pasquier, D. Leys
- Silent MRI infarcts and the risk of future strokeThe cardiovascular health studyC. Bernick, L. Kuller, C. Dulberg, W.T. Longstreth Jr., T. Manolio, N. Beauchamp, T. Price, for the Cardiovascular Health Study Collaborative Research Group*
- Mitochondrial dysfunction associated with a mutation in the Notch3 gene in a CADASIL familyP. de la Peña, B. Bornstein, P. del Hoyo, M. A. Fernández–Moreno, M. A. Martín, Y. Campos, C. Gómez–Escalonilla, J. A. Molina, A. Cabello, J. Arenas, R. Garesse
- Effects of IV methylprednisolone on brain atrophy in relapsing-remitting MSR. Zivadinov, R. A. Rudick, R. De Masi, D. Nasuelli, M. Ukmar, R. S. Pozzi–Mucelli, A. Grop, G. Cazzato, M. Zorzon
- Axonal loss in normal-appearing white matter in a patient with acute MSC. Bjartmar, R. P. Kinkel, G. Kidd, R. A. Rudick, B. D. Trapp
- Optimizing the association between disability and biological markers in MSN. F. Kalkers, E. Bergers, J. A. Castelijns, M. A. A. van Walderveen, J. C. J. Bot, H. J. Adèr, C. H. Polman, F. Barkhof
- Neural and cognitive bases of upper limb apraxia in corticobasal degenerationP. Peigneux, E. Salmon, G. Garraux, S. Laureys, S. Willems, K. Dujardin, C. Degueldre, C. Lemaire, A. Luxen, G. Moonen, G. Franck, A. Destee, M. Van der Linden
- Autism in tuberous sclerosis complex is related to both cortical and subcortical dysfunctionE. Asano, D. C. Chugani, O. Muzik, M. Behen, J. Janisse, R. Rothermel, T. J. Mangner, P. K. Chakraborty, H. T. Chugani
- Molecular heterogeneity of oligodendrogliomas suggests alternative pathways in tumor progressionK. Hoang–Xuan, J. He, S. Huguet, K. Mokhtari, Y. Marie, M. Kujas, P. Leuraud, L. Capelle, J. Y. Delattre, J. Poirier, P. Broët, M. Sanson
- Immune reactivity in a mouse model of familial ALS correlates with disease progressionMaria E. Alexianu, Milena Kozovska, Stanley H. Appel
- Sleep-disordered breathing and respiratory failure in acid maltase deficiencyU. Mellies, R. Ragette, C. Schwake, M. Baethmann, T. Voit, H. Teschler
- Pain increases during sympathetic arousal in patients with complex regional pain syndromePeter D. Drummond, Philip M. Finch, Shiarne Skipworth, Paul Blockey
Views & Reviews
- Arterial dissection and stroke in childrenHeather J. Fullerton, S. Claiborne Johnston, Wade S. Smith
Clinical/Scientific Notes
- Association of a tumor necrosis factor α polymorphism with MS susceptibilityBrian G. Weinshenker, David D. Hebrink, Elizabeth Atkinson, Orhun H. Kantarci
- High frequency of the H63D mutation of the hemochromatosis gene (HFE) in malignant gliomasF. Martinez di Montemuros, D. Tavazzi, E. Salsano, T. Piepoli, B. Pollo, G. Fiorelli, G. Finocchiaro
- Ovarian hyperstimulation syndrome with ischemic stroke due to an intracardiac thrombusG. A. Worrell, E. F.M. Wijdicks, S. D.Z. Eggers, T. Phan, M. A. Damario, C. J. Mullany
- Migrainous aura starting several minutes after the onset of subarachnoid hemorrhageJ. P. Dreier, O. W. Sakowitz, A. W. Unterberg, G. Benndorf, K. M. Einhäupl, J. M. Valdueza
- MRI assessment of spared fibers following callosotomy: A second lookP. M. Corballis, S. Inati, M. G. Funnell, S. T. Grafton, M. S. Gazzaniga
NeuroImages
- Deteriorating parkinsonism and subdural hematomasSamuel M. Chou, Ludwig Gutmann
Correspondence
- HTLV-I associated myelopathy/tropical spastic paraparesis with pseudohypothyroidismReimar Fritzen, Alexander Dressel
- Hallucinations, REM sleep, and Parkinson’s disease: A medical hypothesisRaffaele Manni, Paolo Mazzarello
- Noninvasive ventilation allows gastrostomy tube placement in patients with advanced ALSJulie Rowin, Matthew N. Meriggioli
Corrections
Departments
Filler
Brief Communications
- Dopaminergic neurotransmission and restless legs syndrome: A genetic association analysisA. Desautels, G. Turecki, J. Montplaisir, N. Ftouhi–Paquin, M. Michaud, V.A. Chouinard, G.A. Rouleau
- Normal IPT and IBZM SPECT in drug-naive and levodopa-treated idiopathic restless legs syndromeI. Eisensehr, T. C. Wetter, R. Linke, S. Noachtar, H. v. Lindeiner, F. J. Gildehaus, C. Trenkwalder, K. Tatsch
- SCA8 repeat expansions in ataxia: A controversial associationM.-J. Sobrido, J. A. Cholfin, S. Perlman, S. M. Pulst, D. H. Geschwind
- Long-term treatment with recombinant nerve growth factor for HIV-associated sensory neuropathyG. Schifitto, C. Yiannoutsos, D. M. Simpson, B. T. Adornato, E. J. Singer, H. Hollander, C. M. Marra, M. Rubin, B. A. Cohen, T. Tucker, I. J. Koralnik, D. Katzenstein, B. Haidich, M. E. Smith, S. Shriver, L. Millar, D. B. Clifford, J. C. McArthur, the AIDS Clinical Trials Group Team 291
- Acute sensory ataxic neuropathy associated with monospecific anti-GD1b IgG antibodyC.-L. Pan, N. Yuki, M. Koga, M.-C. Chiang, S.-T. Hsieh
- Congenital muscular dystrophy with primary partial laminin α2 chain deficiency: Molecular studyY. He, K. J. Jones, N. Vignier, G. Morgan, M. Chevallay, A. Barois, B. Estournet–Mathiaud, H. Hori, T. Mizuta, F. M.S. Tomé, K. N. North, P. Guicheney
- Sodium channel gene mutations in hypokalemic periodic paralysis: An uncommon cause in the UKN. P. Davies, L. H. Eunson, M. Samuel, M. G. Hanna
- Fibromyalgia is common in patients with transformed migraineM. F.P. Peres, W. B. Young, A. O. Kaup, E. Zukerman, S. D. Silberstein
- High-grade carotid stenosis detected before general surgery: Is endarterectomy indicated?Bruce A. Evans, Eelco F.M. Wijdicks
- Prognosis after percutaneous closure of patent foramen ovale for paradoxical embolismA. Wahl, B. Meier, B. Haxel, K. Nedeltchev, M. Arnold, E. Eicher, M. Sturzenegger, C. Seiler, H. P. Mattle, S. Windecker
- Improving patient selection for coagulopathy testing in the setting of acute ischemic strokeCheryl D. Bushnell, Zaeem Siddiqi, Larry B. Goldstein
- Status epilepticus due to human parvovirus B19 encephalitis in an immunocompetent adultPeter T. Skaff, David M. Labiner
- rTMS of the unaffected hemisphere transiently reduces contralesional visuospatial hemineglectM. Oliveri, E. Bisiach, F. Brighina, A. Piazza, V. La Bua, D. Buffa, B. Fierro
Historical Note
Nisus: Neurology and the Humanities
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