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Archives of Neurology

March 2008, Vol 65, No. 3
Theme: Neuromics 2008 Part I
Basic View  |  Expanded View
About This Journal FREE
Topics:
Arch Neurol. 2008;65(3):298. doi:10.1001/archneur.65.3.298.
This Month in Archives of Neurology FREE
Topics:
Arch Neurol. 2008;65(3):301-302. doi:10.1001/archneur.65.3.301.
Neuromics
Topics: phenotype, mitochondrial myopathies, down syndrome, epilepsy, parkinson disease, alzheimer's disease, glucose metabolism, nervous system disorder, mutation, amyotrophic lateral sclerosis, polymorphism, dementia, stem cells, fragile x syndrome, acidosis, lactic, amyloid beta-protein precursor, arctic regions, disclosure, dna, mitochondrial, genes, genome, glucosylceramidase, heterozygote, recombinant interferon-gamma, leigh disease, lewy bodies, mental disorders, mothers, multiple sclerosis, nerve conduction function, neurology, parent, sodium channel, brain, genetics, mosaicism, primary lateral sclerosis, encephalopathy, insomnia, fatal familial, thalamic neoplasms, congenital anomaly of brain, mitochondrial dna mutation, grn gene, park2 gene, neurogenetics, self-mutilation by cutting, mapt gene
Arch Neurol. 2008;65(3):304. doi:10.1001/archneur.65.3.304.
Neuromics and Neurological Disease
Topics: nervous system disorder
Arch Neurol. 2008;65(3):307-308. doi:10.1001/archneur.65.3.307.
Correction: Editorial Board News
Topics: parkinson disease, alzheimer's disease, vascular dementia, dementia, dyskinesia, movement disorders, neurodegenerative disorders, neurology
Arch Neurol. 2008;65(3):309. doi:10.1001/archneur.65.3.309.
Stem Cells on the Brain FREE
Paul S. Knoepfler, PhD
Topics: stem cells, chromatin, brain, neural stem cell
Arch Neurol. 2008;65(3):311-315. doi:10.1001/archneur.65.3.311.
The HapMap:  Charting a Course for Genetic Discovery in Neurological Diseases FREE
John Hardy, PhD; Andrew Singleton, PhD
Topics: nervous system disorder, genetics
Arch Neurol. 2008;65(3):319-321. doi:10.1001/archneur.65.3.319.
Retromer Sorting:  A Pathogenic Pathway in Late-Onset Alzheimer Disease FREE
Scott A. Small, MD
Topics: alzheimer's disease, brain, presenilin, molecule
Arch Neurol. 2008;65(3):323-328. doi:10.1001/archneurol.2007.64.
Genome-Wide Association Studies in Alzheimer Disease FREE
Stephen C. Waring, DVM, PhD; Roger N. Rosenberg, MD
Topics: alzheimer's disease, genetics, genome-wide association study
Arch Neurol. 2008;65(3):329-334. doi:10.1001/archneur.65.3.329.
Trial Registration Required FREE
Topics:
Arch Neurol. 2008;65(3):315. doi:10.1001/archneur.65.3.315.
Calendar of Events: A New Web Feature FREE
Topics:
Arch Neurol. 2008;65(3):328. doi:10.1001/archneur.65.3.328.
Full-text Online Access FREE
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Arch Neurol. 2008;65(3):348. doi:10.1001/archneur.65.3.348.
Online Submission and Peer Review System Available FREE
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Arch Neurol. 2008;65(3):357. doi:10.1001/archneur.65.3.357.
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Arch Neurol. 2008;65(3):378. doi:10.1001/archneur.65.3.378.
Topic Collections FREE
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Arch Neurol. 2008;65(3):386. doi:10.1001/archneur.65.3.386.
E-mail Alert FREE
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Arch Neurol. 2008;65(3):392. doi:10.1001/archneur.65.3.392.
E-mail a Friend FREE
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Arch Neurol. 2008;65(3):406. doi:10.1001/archneur.65.3.406.
New Initiatives: Clinical Trials and Videos FREE
Topics:
Arch Neurol. 2008;65(3):419. doi:10.1001/archneur.65.3.419.
Genome-Wide Pharmacogenomic Analysis of the Response to Interferon Beta Therapy in Multiple Sclerosis FREE
Esther Byun, MD; Stacy J. Caillier, BSc; Xavier Montalban, MD; Pablo Villoslada, MD, PhD; Oscar Fernández, MD; David Brassat, MD; Manuel Comabella, MD, PhD; Joanne Wang, MPH; Lisa F. Barcellos, PhD; Sergio E. Baranzini, PhD; Jorge R. Oksenberg, PhD
Includes: CME
Topics: pharmacogenomics, dna, genome, interferon-beta, multiple sclerosis, single nucleotide polymorphism, recombinant interferon-beta
Arch Neurol. 2008;65(3):337-344. doi:10.1001/archneurol.2008.47.
Maternal Transmission of Multiple Sclerosis in a Dutch Population FREE
Ilse A. Hoppenbrouwers, MD; Fan Liu, MD; Yurii S. Aulchenko, PhD; George C. Ebers, MD; Ben A. Oostra, PhD; Cornelia M. van Duijn, PhD; Rogier Q. Hintzen, MD, PhD
Topics: mothers, multiple sclerosis
Arch Neurol. 2008;65(3):345-348. doi:10.1001/archneurol.2007.63.
Interferon Gamma Allelic Variants:  Sex-Biased Multiple Sclerosis Susceptibility and Gene Expression FREE
Orhun H. Kantarci, MD; David D. Hebrink, BA; Janet Schaefer-Klein, BS; Yulong Sun, PhD; Sara Achenbach, MS; Elizabeth J. Atkinson, MS; Shirley Heggarty, PhD; Anne C. Cotleur, MS; Mariza de Andrade, PhD; Koen Vandenbroeck, PhD; Clara M. Pelfrey, PhD; Brian G. Weinshenker, MD
Topics: gene expression, haplotypes, interferon type ii, recombinant interferon-gamma, multiple sclerosis
Arch Neurol. 2008;65(3):349-357. doi:10.1001/archneurol.2007.66.
Cortical Brain Malformations:  Effect of Clinical, Neuroradiological, and Modern Genetic Classification FREE
Marie Claire Yvette de Wit, MD; Maarten H. Lequin, MD, PhD; Ireneaus F. M. de Coo, MD, PhD; Esther Brusse, MD; Dicky J. J. Halley, PhD; Raoul van de Graaf, BSc; Rachel Schot, BSc; Frans W. Verheijen, PhD; Grazia M. S. Mancini, MD, PhD
Topics: epilepsy, mutation, ectopic tissue, microcephaly, genetics, microgyria, lissencephaly, congenital anomaly of brain
Arch Neurol. 2008;65(3):358-366. doi:10.1001/archneur.65.3.358.
The G13513A Mutation in the ND5 Gene of Mitochondrial DNA as a Common Cause of MELAS or Leigh Syndrome:  Evidence From 12 Cases FREE
Sara Shanske, PhD; Jorida Coku, BS; Jiesheng Lu, MD; Jaya Ganesh, MD; Sindu Krishna, PhD; Kurenai Tanji, MD; Eduardo Bonilla, MD; Ali B. Naini, PhD; Michio Hirano, MD; Salvatore DiMauro, MD
Topics: mutation, dna, mitochondrial, genes, leigh disease, melas syndrome
Arch Neurol. 2008;65(3):368-372. doi:10.1001/archneurol.2007.67.
Conjugal Alzheimer Disease:  Risk in Children When Both Parents Have Alzheimer Disease FREE
Suman Jayadev, MD; Ellen J. Steinbart, RN, MA; Yueh-Yun Chi, PhD; Walter A. Kukull, PhD; Gerard D. Schellenberg, PhD; Thomas D. Bird, MD
Topics: alzheimer's disease, parent
Arch Neurol. 2008;65(3):373-378. doi:10.1001/archneurol.2007.61.
Glucocerebrosidase Gene Mutations:  A Risk Factor for Lewy Body Disorders FREE
Ignacio F. Mata, PhD; Ali Samii, MD; Seth H. Schneer; John W. Roberts, MD; Alida Griffith, MD; Berta C. Leis, PhD, RN; Gerard D. Schellenberg, PhD; Ellen Sidransky, MD; Thomas D. Bird, MD; James B. Leverenz, MD; Debby Tsuang, MD, MSc; Cyrus P. Zabetian, MD, MS
Topics: mutation, genes, glucosylceramidase, lewy bodies
Arch Neurol. 2008;65(3):379-382. doi:10.1001/archneurol.2007.68.
A Locus for Primary Lateral Sclerosis on Chromosome 4ptel-4p16.1 FREE
Paul N. Valdmanis, BSc; Nicolas Dupré, MD, MSc; Guy A. Rouleau, MD, PhD
Topics: chromosomes, primary lateral sclerosis
Arch Neurol. 2008;65(3):383-386. doi:10.1001/archneur.65.3.383.
Long-term Follow-up of Taiwanese Chinese Patients Treated Early for 6-Pyruvoyl-Tetrahydropterin Synthase Deficiency FREE
Kai-Ming Liu, MS; Tze-Tze Liu, PhD; Ni-Chung Lee, MD; Ling-Yee Cheng, MS; Kwang-Jen Hsiao, PhD; Dau-Ming Niu, MD, PhD
Topics: phenotype, 5-hydroxytryptophan, birth weight, genotype, levodopa, neurotransmitters, phenylalanine, protein tyrosine phosphatase, cognitive ability, sapropterin, chinese people, post-thoracotomy pain syndrome
Arch Neurol. 2008;65(3):387-392. doi:10.1001/archneur.65.3.387.
Hereditary Spastic Paraplegia With Mental Impairment and Thin Corpus Callosum in Tunisia:  SPG11, SPG15, and Further Genetic Heterogeneity FREE
Amir Boukhris, MD; Giovanni Stevanin, PhD; Imed Feki, MD; Elodie Denis, BS; Nizar Elleuch, MD; Mohamed Imed Miladi, MD; Jérémy Truchetto, BS; Paola Denora, PhD; Samir Belal, MD; Chokri Mhiri, MD; Alexis Brice, MD
Topics: corpus callosum, genetic heterogeneity, spastic paraplegia, hereditary, tunisia, mental state abnormal
Arch Neurol. 2008;65(3):393-402. doi:10.1001/archneur.65.3.393.
Amyotrophic Lateral Sclerosis With Ragged-Red Fibers FREE
Michio Hirano, MD; Corrado Angelini, MD; Pasquale Montagna, MD; Arthur P. Hays, MD; Kurenai Tanji, MD; Hiroshi Mitsumoto, MD; Paul H. Gordon, MD; Ali B. Naini, PhD; Salvatore DiMauro, MD; Lewis P. Rowland, MD
Topics: amyotrophic lateral sclerosis, dna, mitochondrial
Arch Neurol. 2008;65(3):403-406. doi:10.1001/archneurol.2007.65.
Altered Cerebral Glucose Metabolism in a Family With Clinical Features Resembling Mitochondrial Neurogastrointestinal Encephalomyopathy Syndrome in Association With Multiple Mitochondrial DNA Deletions FREE
Fritz-Georg Lehnhardt, MD; Rita Horvath, MD; Roland Ullrich, MD; Lutz Kracht, MD; Jan Sobesky, PhD; Walter Möller-Hartmann, PhD; Andreas H. Jacobs, PhD; Walter F. Haupt, PhD
Topics: glucose metabolism, mitochondria, dna, mitochondrial, brain, fluorodeoxyglucose positron emission tomography
Arch Neurol. 2008;65(3):407-411. doi:10.1001/archneur.65.3.407.
Mosaicism for Trisomy 21 in a Patient With Young-Onset Dementia:  A Case Report and Brief Literature Review FREE
John M. Ringman, MD; P. Nagesh Rao, PhD; Po H. Lu, PsyD; Stephen Cederbaum, MD
Topics: down syndrome, dementia, mosaicism
Arch Neurol. 2008;65(3):412-415. doi:10.1001/archneur.65.3.412.
Archives Express FREE
Roger N. Rosenberg, MD; Roger N. Rosenberg, MD
Topics:
Arch Neurol. 2008;65(3):411. doi:10.1001/archneur.65.3.411.
Rapid Exacerbation in an Elderly Case of Adult-Onset X-linked Adrenoleukodystrophy With Cerebral Corticospinal Tract Involvement
Tsunenori Saito, MD; Tomoyuki Mizuno, MD, PhD; Tomoji Watanabe, MD, PhD; Masayoshi Ida, MD, PhD; Hirofumi Nakase, MD, PhD
Topics: corticospinal tract, adrenoleukodystrophy, brain, elderly
Arch Neurol. 2008;65(3):416. doi:10.1001/archneur.65.3.416.
The Consciousness Dilemma: Feel or Feel of Feeling?
Marco Sarà, MD; Francesca Pistoia, MD; Giuseppe Cernera, MD; Simona Sacco, MD
Topics: consciousness related finding
Arch Neurol. 2008;65(3):418. doi:10.1001/archneur.65.3.418-a.
The Consciousness Dilemma: Feel or Feel of Feeling?—Reply
Adrian M. Owen, PhD; Martin R. Coleman, PhD; Melanie Boly, MD; Matthew H. Davis, PhD; Steven Laureys, MD; John D. Pickard, MD
Topics: consciousness related finding
Arch Neurol. 2008;65(3):418-419. doi:10.1001/archneur.65.3.418-b.
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