In This Issue
Editorial
- Rett syndrome “We’ll keep the genes on for you”Harvey S. Singer, SakkuBai Naidu
Articles
- Baclofen treatment in Tourette syndromeA double-blind, placebo-controlled, crossover trialHarvey S. Singer, John Wendlandt, Madeline Krieger, Joseph Giuliano
- Botulinum toxin for simple motor ticsA randomized, double-blind, controlled clinical trialConnie Marras, David Andrews, Elspeth Sime, Anthony E. Lang
- MECP2 gene analysis in classical Rett syndrome and in patients with Rett-like featuresM. Auranen, R. Vanhala, M. Vosman, M. Levander, T. Varilo, M. Hietala, R. Riikonen, L. Peltonen, I. Järvelä
- Cognitive status and quality of life in patients with suspected versus proven low-grade gliomasJ.C. Reijneveld, M.M. Sitskoorn, M. Klein, J. Nuyen, M.J.B. Taphoorn
- Use of specialized coagulation testing in the evaluation of patients with acute ischemic strokeCheryl Bushnell, Zaeem Siddiqi, Joel C. Morgenlander, Larry B. Goldstein
- MRI hyperintensities of the temporal lobe and external capsule in patients with CADASILM. O’Sullivan, J.M. Jarosz, R.J. Martin, N. Deasy, J.F. Powell, H.S. Markus
- Altered white and gray matter metabolism in CADASILA proton MR spectroscopy and 1H-MRSI studyD. P. Auer, T. Schirmer, J. O. Heidenreich, J. Herzog, B. Pütz, M. Dichgans
- Occipital hypoperfusion on SPECT in dementia with Lewy bodies but not ADK. Lobotesis, J.D. Fenwick, A. Phipps, A. Ryman, A. Swann, C. Ballard, I.G. McKeith, J.T. O’Brien
- Gender differences in predictors of mortality in nursing home residents with ADK.L. Lapane, G. Gambassi, F. Landi, A. Sgadari, V. Mor, R. Bernabei
- APOE-ε4 is associated with weight loss in women with ADA population-based studyM. Vanhanen, M. Kivipelto, K. Koivisto, J. Kuusisto, L. Mykkänen, E.-L. Helkala, T. Hänninen, K. Kervinen, Y.A. Kesäniemi, M.P. Laakso, H. Soininen, M. Laakso
- Calpain-3 and dysferlin protein screening in patients with limb–girdle dystrophy and myopathyM. Fanin, E. Pegoraro, C. Matsuda–Asada, R.H. Brown, C. Angelini
- Serum levels of tumor necrosis factor–α in chronic inflammatory demyelinating polyneuropathyS. Misawa, S. Kuwabara, M. Mori, N. Kawaguchi, Y. Yoshiyama, T. Hattori
Views & Reviews
- Magnetic resonance spectroscopy in ADMichael J. Valenzuela, Perminder Sachdev
Clinical/Scientific Notes
- Normal calpain expression in genetically confirmed limb–girdle muscular dystrophy type 2AB. Talim, A. Ognibene, E. Mattioli, I. Richard, L.V.B. Anderson, L. Merlini
- Is Epstein–Barr virus present in the CNS of patients with MS?S.A. Morré, J. van Beek, C.J.A. De Groot, J. Killestein, C.J.L.M. Meijer, C.H. Polman, P. van der Valk, J.M. Middeldorp, A.J.C. van den Brule
- Bilateral middle cerebellar peduncle infarction caused by traumatic vertebral artery dissectionK. Akiyama, S. Takizawa, K. Tokuoka, Y. Ohnuki, N. Kobayashi, Y. Shinohara
NeuroImages
- Leukoaraiosis three–dimensional in Binswanger diseaseCarlos Valencia, Joan Martí–Fàbregas, Jesús Pujol Nuez, Josep–Lluis Martí–Vilalta
- Reversible pontine edema in hypertensionCornelia Drees, Luay Alkotob, Philip M. Hall, Derk Krieger
- Disappearing “face of the giant panda”Alessandro Stefano Zagami, Peter Michael Boers
Correspondence
- Practice parameter: Risk of driving and Alzheimer’s diseaseDaniel Foley, Kamal Masaki, Lon White, G. Webster Ross, John Eberhard
- Chenodeoxycholic treatment of cerebrotendinous xanthomatosisPaul Samenuk, Boyd M. Koffman
Calendar
Special Articles
- A profile of neurology practice based on Medicare servicesAn AAN Medical Economics and Management Committee ReportMarc R. Nuwer, Michele Duncan, Jamie M. Nuwer
Brief Communications
- Restoring blood pressure reperfused Wernicke’s area and improved languageA.E. Hillis, P.B. Barker, N.J. Beauchamp, B.D. Winters, M. Mirski, R.J. Wityk
- Aldosterone synthase (CYP11B2) gene polymorphism and cerebral white matter hyperintensitiesP. Verpillat, A. Alpérovitch, F. Cambien, V. Besançon, H. Desal, C. Tzourio
- Evidence for genetic heterogeneity in hereditary neuralgic amyotrophyG.D.J. Watts, K.C. O’Briant, T.E. Borreson, A.J. Windebank, P.F. Chance
- Chronic encephalitis and temporal lobe epilepsy: A variant of Rasmussen’s syndrome?M.J. Hennessy, M. Koutroumanidis, A.F. Dean, J. Jarosz, R.D.C. Elwes, C.D. Binnie, C.E. Polkey
- Catathrenia (nocturnal groaning): A new type of parasomniaR. Vetrugno, F. Provini, G. Plazzi, L. Vignatelli, E. Lugaresi, P. Montagna
- Continuous vertigo and spontaneous nystagmus due to canalolithiasis of the horizontal canalMichael von Brevern, Andrew H. Clarke, Thomas Lempert
- The T9176G mtDNA mutation severely affects ATP production and results in Leigh syndromeR. Carrozzo, A. Tessa, M.E. Vázquez–Memije, F. Piemonte, C. Patrono, A. Malandrini, C. Dionisi–Vici, L. Vilarinho, M. Villanova, H. Schägger, A. Federico, E. Bertini, F.M. Santorelli
Advertisement
Popular on
Neurology

Use of Whole-Genome Sequencing for Mitochondrial Disease Diagnosis
Dr. Robert Pitceathly and Dr. William Macken
► Watch
Advertisement