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  • Use of Recommended Neurodiagnostic Evaluation Among Patients With Drug-Resistant Epilepsy

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    ÁñÁ«ÊÓƵ Neurol. 2024; 81(5):499-506. 10.1001/jamaneurol.2024.0551

    This cross-sectional study examines the use of neurodiagnostic testing among patients with drug-resistant epilepsy.

  • The Role of Cardiovascular Risk Factors and Stroke in Familial Alzheimer Disease

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    ÁñÁ«ÊÓƵ Neurol. 2016; 73(10):1231-1237. 10.1001/jamaneurol.2016.2539

    This cohort study investigates associations between coronary risk factors, stroke, and late-onset Alzheimer dementia in patients with familial disease.

  • Age-Specific Incidence Rates for Dementia and Alzheimer Disease in NIA-LOAD/NCRAD and EFIGA Families: National Institute on Aging Genetics Initiative for Late-Onset Alzheimer Disease/National Cell Repository for Alzheimer Disease (NIA-LOAD/NCRAD) and Estudio Familiar de Influencia Genetica en Alzheimer (EFIGA)

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    ÁñÁ«ÊÓƵ Neurol. 2014; 71(3):315-323. 10.1001/jamaneurol.2013.5570

    Vardarajan et al determine the incidence rates of dementia and Alzheimer disease in unaffected family members in the NIA-LOAD/NCRAD and EFIGA family studies.

  • Cognitive and Motor Function in Long-Duration PARKIN -Associated Parkinson Disease

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    ÁñÁ«ÊÓƵ Neurol. 2014; 71(1):62-67. 10.1001/jamaneurol.2013.4498

    In a cross-sectional study of 44 participants with early-onset PD of long duration, Alcalay and coauthors assessed cognitive and motor performances, comparing homozygotes and compound heterozygotes who carry 2 PARKIN mutations with noncarriers.

  • Use of Anterior Temporal Lobectomy for Epilepsy in a Community-Based Population

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    Arch Neurol. 2012; 69(11):1476-1481. 10.1001/archneurol.2012.1200
    In a population-based cohort study, Van Gompel et al assess the hypothesis that use of anterior temporal lobectomy for temporal epilepsy has diminished over time.
  • Frequency of Known Mutations in Early-Onset Parkinson Disease: Implication for Genetic Counseling: The Consortium on Risk for Early Onset Parkinson Disease Study

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    Arch Neurol. 2010; 67(9):1116-1122. 10.1001/archneurol.2010.194
  • Predictors of Parkin Mutations in Early-Onset Parkinson Disease: The Consortium on Risk for Early-Onset Parkinson Disease Study

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    Arch Neurol. 2010; 67(6):731-738. 10.1001/archneurol.2010.95
  • Motor Phenotype of LRRK2 G2019S Carriers in Early-Onset Parkinson Disease

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    Arch Neurol. 2009; 66(12):1517-1522. 10.1001/archneurol.2009.267
  • Risk of Parkinson Disease in Carriers of Parkin Mutations: Estimation Using the Kin-Cohort Method

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    Arch Neurol. 2008; 65(4):467-474. 10.1001/archneur.65.4.467
  • Case-Control Study of the Parkin Gene in Early-Onset Parkinson Disease

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    Arch Neurol. 2006; 63(4):548-552. 10.1001/archneur.63.4.548
  • Lack of Familial Aggregation of Parkinson Disease and Alzheimer Disease

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    Arch Neurol. 2004; 61(7):1033-1039. 10.1001/archneur.61.7.1033
  • Mild Tremor in Relatives of Patients With Essential Tremor: What Does This Tell Us About the Penetrance of the Disease?

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    Arch Neurol. 2001; 58(10):1584-1589. 10.1001/archneur.58.10.1584
  • Familial Aggregation of Alzheimer Disease Among Whites, African Americans, and Caribbean Hispanics in Northern Manhattan

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    Arch Neurol. 2000; 57(1):72-77. 10.1001/archneur.57.1.72
  • Parkinson Disease in Twins—Reply

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    JAMA. 1999; 282(14):1328-1329. 10-1001/pubs.JAMA-ISSN-0098-7484-282-14-jbk1013
  • Parkinson Disease in Twins: An Etiologic Study

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    JAMA. 1999; 281(4):341-346. 10-1001/pubs.JAMA-ISSN-0098-7484-281-4-joc81035
  • Are Generalized and Localization-Related Epilepsies Genetically Distinct?

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    Arch Neurol. 1998; 55(3):339-344. 10.1001/archneur.55.3.339