Skip to main content
Advertisement
  • Neurology.org
  • Journals
    • Neurology
    • Clinical Practice
    • Education
    • Genetics
    • Neuroimmunology & Neuroinflammation
  • Online Sections
    • Neurology Video Journal Club
    • Inclusion, Diversity, Equity, Anti-racism, & Social Justice (IDEAS)
    • Innovations in Care Delivery
    • Practice Buzz
    • Practice Current
    • Residents & Fellows
    • Without Borders
  • Collections
    • COVID-19
    • Disputes & Debates
    • Health Disparities
    • Infographics
    • Null Hypothesis
    • Patient Pages
    • Translations
    • Topics A-Z
  • Podcast
  • CME
  • About
    • About the Journals
    • Contact Us
    • Editorial Board
  • Authors
    • Submit a Manuscript
    • Author Center

Advanced Search

Main menu

  • Neurology.org
  • Journals
    • Neurology
    • Clinical Practice
    • Education
    • Genetics
    • Neuroimmunology & Neuroinflammation
  • Online Sections
    • Neurology Video Journal Club
    • Inclusion, Diversity, Equity, Anti-racism, & Social Justice (IDEAS)
    • Innovations in Care Delivery
    • Practice Buzz
    • Practice Current
    • Residents & Fellows
    • Without Borders
  • Collections
    • COVID-19
    • Disputes & Debates
    • Health Disparities
    • Infographics
    • Null Hypothesis
    • Patient Pages
    • Translations
    • Topics A-Z
  • Podcast
  • CME
  • About
    • About the Journals
    • Contact Us
    • Editorial Board
  • Authors
    • Submit a Manuscript
    • Author Center
  • Home
  • Articles
  • Issues

User menu

  • My Alerts
  • Log in

Search

  • Advanced search
Neurology Genetics
Home
A peer-reviewed clinical and translational neurology open access journal
  • My Alerts
  • Log in
Site Logo
  • Home
  • Articles
  • Issues

Latest Articles

  • Article
    Dysfunctional ADAM22 implicated in progressive encephalopathy with cortical atrophy and epilepsy
    Mikko Muona, Yuko Fukata, Anna-Kaisa Anttonen, et al.
    January 21, 2016
  • Clinical/Scientific Notes
    Co-occurrence of 16p13.11 microdeletion and ring chromosome 20 syndrome
    Lance H. Rodan, Maria Zak, James Stavropoulos, et al.
    January 14, 2016
  • Article
    Overlap between Parkinson disease and Alzheimer disease in ABCA7 functional variants
    Karen Nuytemans, Lizmarie Maldonado, Aleena Ali, et al.
    January 14, 2016
  • Article
    Segregation of a rare TTC3 variant in an extended family with late-onset Alzheimer disease
    Martin A. Kohli, Holly N. Cukier, Kara L. Hamilton-Nelson, et al.
    January 14, 2016
  • Article
    In silico prioritization based on coexpression can aid epileptic encephalopathy gene discovery
    Karen L. Oliver, Vesna Lukic, Saskia Freytag, et al.
    January 14, 2016
  • Article
    Atypical parkinsonism caused by Pro105Leu mutation of prion proteinA broad clinical spectrum
    Kagari Koshi Mano, Takashi Matsukawa, Jun Mitsui, et al.
    January 07, 2016
  • Clinical/Scientific Notes
    Polyneuropathy in a young Belgian patient: A novel heterozygous mutation in the WNK1/HSN2 gene
    Jeroen de Filette, Danielle Hasaerts, Sara Seneca, et al.
    January 07, 2016
  • The Helix
    Whole-exome sequencing in neurologic practiceReducing the diagnostic odyssey
    Nicholas E. Johnson
    December 24, 2015
  • Clinical/Scientific Notes
    Late diagnosis of cerebral folate deficiency: Fewer seizures with folinic acid in adult siblings
    Patrick Ferreira, Stephanie M. Luco, Sarah L. Sawyer, et al.
    December 23, 2015
  • Clinical/Scientific Notes
    Benign hereditary chorea related to NKX2-1 with ataxia and dystonia
    Claudio M. de Gusmao, Fernando Kok, Erasmo Barbante Casella, et al.
    December 23, 2015

Pages

  • First
  • Previous
  • …
  • 62
  • 63
  • 64
  • 65
  • 66
  • 67
  • 68
  • 69
  • 70
  • Next
  • Last
Advertisement

Preferences and User Experiences of Wearable Devices in Epilepsy A Systematic Review and Mixed-Methods Synthesis

Dr. Daniel Friedman and Dr. Sharon Chiang

► Watch

Neurology Genetics: 9 (2)

Articles

  • Articles
  • Issues
  • Popular Articles

About

  • About the Journals
  • Ethics Policies
  • Editors & Editorial Board
  • Contact Us
  • Advertise

Submit

  • Author Center
  • Submit a Manuscript
  • Information for Reviewers
  • AAN Guidelines
  • Permissions

Subscribers

  • Subscribe
  • Sign up for eAlerts
  • RSS Feed
Site Logo
  • Visit neurology Template on Facebook
  • Follow neurology Template on Twitter
  • Visit Neurology on YouTube
  • Neurology
  • Neurology: Clinical Practice
  • Neurology: Education
  • Neurology: Genetics
  • Neurology: Neuroimmunology & Neuroinflammation
  • AAN.com
  • AANnews
  • Continuum
  • Brain & Life
  • Neurology Today

Wolters Kluwer Logo

Neurology: Genetics | Online ISSN: 2376-7839

© 2023 American Academy of Neurology

  • Privacy Policy
  • Feedback
  • Advertise