November 1, 2001 Issue of JAMA Neurology

November 2001, Vol 58, No. 11, Pages 1736-1944 | Neurogenetics/Neurogenomics 2001

Editorial

Genomic Neurology: A New Beginning

Roger N. Rosenberg, MD

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Arch Neurol. 2001;58(11):1739-1741. doi:10.1001/archneur.58.11.1739

The Human Genome Is Sequenced: What Does It Mean and Why Is It Important?

John Hardy, PhD

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Arch Neurol. 2001;58(11):1748-1749. doi:10.1001/archneur.58.11.1748

Impact of the Human Genome Sequence on Neurology and Neuroscience

Imke Puls, MD; Andrew P. Lieberman, MD, PhD; Kenneth H. Fischbeck, MD

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Arch Neurol. 2001;58(11):1750-1751. doi:10.1001/archneur.58.11.1750

Genomes, Neuroscience, and Neurology

Stefan-M. Pulst, MD, Dr Med

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Arch Neurol. 2001;58(11):1755-1757. doi:10.1001/archneur.58.11.1755

Neurogenetics in the Postgenomic Era

Shoji Tsuji, MD, PhD

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Arch Neurol. 2001;58(11):1758-1759. doi:10.1001/archneur.58.11.1758

Thoughts on the Relationship of the Human Genome Project to Neurology

Thomas D. Bird, MD

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Arch Neurol. 2001;58(11):1764-1765. doi:10.1001/archneur.58.11.1764

2025: The Practice of Neurology: Back From the Future

Allen D. Roses, MD

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Arch Neurol. 2001;58(11):1766-1767. doi:10.1001/archneur.58.11.1766

Original Contribution

The Genetic and Pathological Classification of Familial Frontotemporal Dementia

Huw R. Morris, MRCP; M. Nadeem Khan, MSc; John C. Janssen, MRCP; et al.

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Arch Neurol. 2001;58(11):1813-1816. doi:10.1001/archneur.58.11.1813

伪-Synuclein in Familial Alzheimer Disease: Epitope Mapping Parallels Dementia With Lewy Bodies and Parkinson Disease

Carol F. Lippa, MD; M. Luise Schmidt, PhD; Virginia M.-Y. Lee, PhD; et al.

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Arch Neurol. 2001;58(11):1817-1820. doi:10.1001/archneur.58.11.1817

Improvement in the Molecular Diagnosis of Machado-Joseph Disease

Patrícia Maciel, PhD; Maria do Carmo Costa, BSc; Anabela Ferro, BSc; et al.

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Arch Neurol. 2001;58(11):1821-1827. doi:10.1001/archneur.58.11.1821

Impact of DNA Testing for Early-Onset Familial Alzheimer Disease and Frontotemporal Dementia

Ellen J. Steinbart, RN, MA; Corrine O. Smith, MS; Parvoneh Poorkaj, PhD; et al.

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Arch Neurol. 2001;58(11):1828-1831. doi:10.1001/archneur.58.11.1828

The SCA12 Mutation as a Rare Cause of Spinocerebellar Ataxia

Jeremy A. Cholfin, BS; María-Jesús Sobrido, MD, PhD; Susan Perlman, MD; et al.

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Arch Neurol. 2001;58(11):1833-1835. doi:10.1001/archneur.58.11.1833

Clinical and Molecular Correlations in Spinocerebellar Ataxia Type 6: A Study of 24 Dutch Families

Richard J. Sinke, PhD; Elly F. Ippel, MD; Conny M. Diepstraten, BSc; et al.

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Arch Neurol. 2001;58(11):1839-1844. doi:10.1001/archneur.58.11.1839

Familial Progressive supranuclear Palsy: Detection of Subclinical Cases Using ¹⁸F-Dopa and ¹⁸Fluorodeoxyglucose Positron Emission Tomography

Paola Piccini, MD; Justo de Yebenez, MD; Andrew J. Lees, MD; et al.

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Arch Neurol. 2001;58(11):1846-1851. doi:10.1001/archneur.58.11.1846

Genetic and Clinical Analysis of Spinocerebellar Ataxia Type 8 Repeat Expansion in Italy

Elena Cellini, PhD; Benedetta Nacmias, PhD; Paolo Forleo, MD; et al.

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Arch Neurol. 2001;58(11):1856-1859. doi:10.1001/archneur.58.11.1856

Dorsal Forebrain Anomaly in Williams Syndrome

Albert M. Galaburda, MD; J. Eric Schmitt, BS; Scott W. Atlas, MD; et al.

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Arch Neurol. 2001;58(11):1865-1869. doi:10.1001/archneur.58.11.1865

TAU as a Susceptibility Gene for Amyotropic Lateral Sclerosis鈥揚arkinsonism Dementia Complex of Guam

Parvoneh Poorkaj, PhD; Debby Tsuang, MD; Ellen Wijsman, PhD; et al.

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Arch Neurol. 2001;58(11):1871-1878. doi:10.1001/archneur.58.11.1871

Identification of a High Frequency of Mutation at Exon 8 of the ATP7B Gene in a Chinese Population With Wilson Disease by Fluorescent PCR

Pingyi Xu, MD, PhD; Xiuling Liang, MD; Joseph Jankovic, MD; et al.

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Arch Neurol. 2001;58(11):1879-1882. doi:10.1001/archneur.58.11.1879

Hearing Impairment Is Common in Various Phenotypes of the Mitochondrial DNA A3243G Mutation

Marcus Deschauer, MD; Tobias Müller, MD; Thomas Wieser, MD; et al.

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Arch Neurol. 2001;58(11):1885-1888. doi:10.1001/archneur.58.11.1885

Images in Neurology

Crossed Cerebrocerebellar Atrophy

Du拧ko Kozi膰, MD; Vladimir S. Kosti膰, MD, PhD

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Arch Neurol. 2001;58(11):1929-1930. doi:10.1001/archneur.58.11.1929

Observation

Clinical and Molecular Studies in a Family With Probable X-linked Dominant Charcot-Marie-Tooth Disease Involving the Central Nervous System

Fuki M. Hisama, MD; Helen H. Lee, BS; Amy Vashlishan; et al.

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Arch Neurol. 2001;58(11):1891-1896. doi:10.1001/archneur.58.11.1891

A New PRNP Mutation (G131V) Associated With Gerstmann-Str盲ussler-Scheinker Disease

Peter K. Panegyres, PhD, FRACP; Kathrine Toufexis, BSc (Hons); B. A. Kakulas, MD, FRCPA, FRACP; et al.

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Arch Neurol. 2001;58(11):1899-1902. doi:10.1001/archneur.58.11.1899

Dentatorubropallidoluysian Atrophy in Chinese

I-Hui Lee, MD; Bing-Wen Soong, MD, PhD; Yi-Chun Lu, BS; et al.

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Arch Neurol. 2001;58(11):1905-1908. doi:10.1001/archneur.58.11.1905

A Case of Familial Amyloid Polyneuropathy Homozygous for the Transthyretin Val30Met Gene With Motor-Dominant Sensorimotor Polyneuropathy and Unusual Sural Nerve Pathological Findings

Akira Yoshioka, MD; Yoko Yamaya, MD; Shinji Saiki, MD; et al.

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Arch Neurol. 2001;58(11):1914-1918. doi:10.1001/archneur.58.11.1914

Complement Factor I Deficiency Associated With Recurrent Meningitis Coinciding With Menstruation

Carolina González-Rubio, PhD; Antonio Ferreira-Cerdán, MD, PhD; Isabel M. Ponce, BS; et al.

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Arch Neurol. 2001;58(11):1923-1928. doi:10.1001/archneur.58.11.1923

Book Reviews

The Private Life of the Brain

Solomon L. Moshé, MD

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Arch Neurol. 2001;58(11):1936. doi:

Pathology of Tumors of the Central Nervous System: A Guide to Histologic Diagnosis

Rosenfeld Myrna, MD, PhD

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Arch Neurol. 2001;58(11):1936-1937. doi:

This Month in Archives of Neurology

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Arch Neurol. 2001;58(11):1736-1738. doi:10.1001/archneur.58.11.1736

Basic Science Seminars in Neurology

Sequence Analysis of the Human Genome: Implications for the Understanding of Nervous System Function and Disease

Anibal Cravchik, MD, PhD; G. Subramanian, MD, PhD; Samuel Broder, MD; et al.

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Arch Neurol. 2001;58(11):1772-1778. doi:10.1001/archneur.58.11.1772

Current Understanding of the Circadian Clock and the Clinical Implications for Neurological Disorders

Fred W. Turek, PhD; Christine Dugovic, PhD; Phyllis C. Zee, MD, PhD

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Arch Neurol. 2001;58(11):1781-1787. doi:10.1001/archneur.58.11.1781

Neurological Review

Polymorphisms in Inflammatory Genes and the Risk of Alzheimer Disease

Patrick L. McGeer, MD, PhD; Edith G. McGeer, PhD

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Arch Neurol. 2001;58(11):1790-1792. doi:10.1001/archneur.58.11.1790

Neurotherapeutics

Feasibility of Gene Therapy for Late Neuronal Ceroid Lipofuscinosis

Dolan Sondhi, PhD; Neil R. Hackett, PhD; Robin L. Apblett, BA; et al.

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Arch Neurol. 2001;58(11):1793-1798. doi:10.1001/archneur.58.11.1793

Special Article

Clinical and Pathological Diagnosis of Frontotemporal Dementia: Report of the Work Group on Frontotemporal Dementia and Pick's Disease

Guy M. McKhann, MD; Marilyn S. Albert, PhD; Murray Grossman, MD, PhD; et al.

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Arch Neurol. 2001;58(11):1803-1809. doi:10.1001/archneur.58.11.1803

History of Neurology

Unraveling the Neuron Jungle: The 1879-1886 Publications by Wilhelm His on the Embryological Development of the Human Brain

Elan D. Louis, MD, MS; Christian Stapf, MD

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Arch Neurol. 2001;58(11):1932-1935. doi:10.1001/archneur.58.11.1932

Letters to the Editor

Cerebrovascular Disease Affects Noncognitive Symptoms in Alzheimer Disease

Giovanni B. Frisoni, MD; Cristina Geroldi, MD, PhD

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Arch Neurol. 2001;58(11):1939-1940. doi:

In reply

Leon J. Thal, MD

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Arch Neurol. 2001;58(11):1939-1940. doi:

Calendar

November 2001-March 2002

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Arch Neurol. 2001;58(11):1941. doi:10.1001/archneur.58.11.1941

Archives CME

Archives of Neurology Reader's Choice: Continuing Medical Education

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Arch Neurol. 2001;58(11):1942-1944. doi:10.1001/archneur.58.11.1942

October 2024 - July 1959

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November 2001, Vol 58, No. 11, Pages 1736-1944 | Neurogenetics/Neurogenomics 2001