m.ng.neurology.orgNeurology Genetics | A peer-reviewed clinical and translational neurology open access journal
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Skip to main content Advertisement Neurology.org Journals Neurology Clinical Practice Genetics Neuroimmunology & Neuroinflammation Specialty Sites Equity, Diversity, and Inclusion Innovations in Care Delivery Without Borders Collections Topics A-Z Residents & Fellows Infographics Patient Pages Null Hypothesis Translations Podcast CME About About the Journals Contact Us Editorial Board Authors Submit a Manuscript Author Center Advanced Search Search for this keyword Main menu Neurology.org Journals Neurology Clinical Practice Genetics Neuroimmunology & Neuroinflammation Specialty Sites Equity, Diversity, and Inclusion Innovations in Care Delivery Without Borders Collections Topics A-Z Residents & Fellows Infographics Patient Pages Null Hypothesis Translations 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 Search for this keyword Advanced search A peer-reviewed clinical and translational neurology open access journal My Alerts Log in Home Articles Issues Announcements COVID-19 specialty site! Features latest articles, invited commentaries, and informative podcasts Neurology: Genetics Impact Factor Announced! 3.509 Call for Authors! Submit your work to Neurology: Genetics ! Notable This Week February 2021; 7(1) Selected by Stefan M. Pulst, MD, Dr med, Editor ARTICLE |Silver-Russell Syndrome Blended Phenotype of Silver-Russell Syndrome and SPG50 Caused by Maternal Isodisomy of Chromosome 7 REVIEW |Genetics Neurology: Genetics Year in Review ARTICLE |Neurovascular Disease MAP3K6 Mutations in a Neurovascular Disease Causing Stroke, Cognitive Impairment, and Tremor ARTICLE |CEDNIK Syndrome New Cohort of Patients With CEDNIK Syndrome Expands the Phenotypic and Genotypic Spectra View Table of Contents Latest Articles Clinical/Scientific Notes Erythromelalgia: A Child With V400M Mutation in the SCN9A Gene Chineze Nwebube , Sabrina Bulancea , Adrian Marchidann , et al. March 01, 2021 Article Interactive Effects of HLA and GM Alleles on the Development of Alzheimer Disease Janardan P. Pandey , Paul J. Nietert , Ronald T. Kothera , et al. February 16, 2021 Article Clonal Evolution of a High-Grade Pediatric Glioma With Distant Metastatic Spread Eliana Marinari , Valerie Dutoit , Sergey Nikolaev , et al. February 15, 2021 Correction V374A KCND3 Pathogenic Variant Associated With Paroxysmal Ataxia Exacerbations February 11, 2021 The Helix Neurology: Genetics Year in Review Stefan Pulst , Massimo Pandolfo , Raymond Roos , et al. February 08, 2021 Clinical/Scientific Notes PRPS1 Gene Mutation Causes Complex X-Linked Adult-Onset Cerebellar Ataxia in Women Flávio M. Rezende Filho , Mariana M. Palma , José Luiz Pedroso , et al. February 03, 2021 View more latest articles Advancing EDI Awareness New Post The Tenure that Requires No Effort Sara Din, MSc View Site Advances in Neurologic Care* New Post Time for a new cost-effectiveness metric By John P. Ney, MD, MPH| December 1, 2020 View Site Advances in Global Neurology New Post Can Global Health Diplomacy Reduce the Global Burden of Brain Disorders? Gretchen L. Birbeck, MD, MPH | November 25, 2020 View Site Advertisement Disease Modifying Therapy in Alzheimer’s Disease; Tenecteplase vs Alteplase in Basilar Occlusion Dr. Jason Crowell talks to Dr. Erik Musiek about disease-modifying therapy in Alzheimer disease. Dr. Andrew Southerland talks with Dr. Fana Alemseged about tenecteplase versus alteplase in basilar artery occlusion. March 2, 2021 Issue Neurology, Journal, Podcast Listen 25:04 Disclosures View Recent Podcasts Follow Visit neurology Template on Facebook Follow neurology Template on Twitter Visit Neurology on YouTube Advertisement Popular on Neurology: Genetics Most Read Most Cited MAP3K6 Mutations in a Neurovascular Disease Causing Stroke, Cognitive Impairment, and Tremor Possible Somatic Mosaicism of Novel FUS Variant in Familial Amyotrophic Lateral Sclerosis Neurology: Genetics Year in Review PRPS1 Gene Mutation Causes Complex X-Linked Adult-Onset Cerebellar Ataxia in Women Mutation in POLR3K causes hypomyelinating leukodystrophy and abnormal ribosomal RNA regulation More... Call for Authors Submit your work to Neurology: Genetics! Back to top 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 Visit neurology Template on Facebook Follow neurology Template on Twitter Visit Neurology on YouTube Neurology Neurology: Clinical Practice Neurology: Genetics Neurology: Neuroimmunology & Neuroinflammation AAN.com AANnews Continuum Brain & Life Neurology Today Neurology: Genetics | Online ISSN: 2376 - 7839 © 2021 American Academy of Neurology Privacy Policy Feedback Advertise...
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