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Vidhyayana - An International Multidisciplinary Peer-Reviewed E-Journal - ISSN 2454-8596 j.vidhyayanaejournal.org |
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Neurology Genetics | A peer-reviewed clinical and translational neurology open access journal m.ng.neurology.org |
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Latest Articles | Neurology Genetics https://ng.neurology.org/content/latest |
About Neurology | Neurology Genetics https://ng.neurology.org/content/about-neurology |
Submit a Peer Review | Neurology Genetics https://ng.neurology.org/submit/peerreview |
Neurology: Genetics' New Mission, Vision, and Scope https://ng.neurology.org/mission-vision |
Archive of all online content | Neurology Genetics https://ng.neurology.org/content/tab-article-info |
Editors & Editorial Board | Neurology Genetics https://ng.neurology.org/about/editors_and_editorial_board |
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Neurology Genetics Volume 3, Number 1_Supplement_1 https://ng.neurology.org/content/3/1_Supplement_1 |
Neurology Genetics Volume 5, Number 4 https://ng.neurology.org/content/5/4 |
Proceedings of the 25th International Stroke Genetics ... https://ng.neurology.org/content/6/1_Supplement_1/e421.abstract |
Proceedings of the 26th International Stroke Genetics ... https://ng.neurology.org/content/6/1_supplement_1/e422.abstract |
Transcriptome and Genome Analysis Uncovers a DMD ... https://ng.neurology.org/content/nng/9/2/e200064.full-text.pdf |
Patients | Neurology Genetics https://ng.neurology.org/content/patients |
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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 Search for this keyword Advanced SearchNeurology.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 Dr. José G. Merino New Editor-in-Chief of Neurology in April 2020 Most Read Article Clinical and experimental studies of a novel P525R FUS mutation in amyotrophic lateral sclerosis Call for Authors! Submit your work to Neurology: Genetics! Notable This Week February 2020; 5(7) Selected by Stefan M. Pulst, MD, Dr med, Editor ARTICLE | Mitochondrial Disorders Expanding the molecular and phenotypic spectrum of truncating MT-ATP6 mutations ARTICLE | Parkinson Disease Analysis of common and rare VPS13C variants in late-onset Parkinson disease ARTICLE |Epilepsy Early infantile epileptic-dyskinetic encephalopathy due to biallelic PIGP mutations ARTICLE |Spinal Muscular Atrophy Analysis of FUS, PFN2, TDP-43, and PLS3 as potential disease severity modifiers in spinal muscular atrophy View Table of Contents Latest Articles Article Use of local genetic ancestry to assess TOMM40 -523′ and risk for Alzheimer disease Parker L. Bussies , Farid Rajabli , Anthony Griswold , et al. 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Birbeck, MD, MPH View Site Advertisement Breastmilk transfer of Rituximab; modeling the price of good health Dr. David Lapides talks with Dr. Riley Bove about his paper on her paper on minimal breastmilk transfer of rituximab, a monoclonal antibody used in neurological conditions March 3, 2020 Issue Neurology, Journal, podcast Listen 20:19 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 Mutation in POLR3K causes hypomyelinating leukodystrophy and abnormal ribosomal RNA regulation Psychometric properties of the Friedreich Ataxia Rating Scale Analysis of FUS , PFN2, TDP-43 , and PLS3 as potential disease severity modifiers in spinal muscular atrophy Yield of comparative genomic hybridization microarray in pediatric neurology practice Clinical features and outcome of 6 new patients carrying de novo KCNB1 gene mutations More... 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