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Nature Reviews. Neurology|November 17, 2018
Author Correction: Neuroimmune disorders of the central nervous system in children in the molecular eraElizabeth Wells, Yael Hacohen, Amy Waldman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 27, 2017
Molecular genetic findings and clinical correlations in 100 patients with Joubert syndrome and related disorders prospectively evaluated at a single centerThierry Vilboux, Daniel A Doherty, Ian A Glass, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|May 3, 2019
Pediatric CNS-isolated hemophagocytic lymphohistiocytosisLeslie A Benson, Hojun Li, Lauren A Henderson, et al.
Annals of Clinical and Translational Neurology|January 13, 2017
Biallelic <i>SCN10A</i> mutations in neuromuscular disease and epileptic encephalopathyMarios Kambouris, Julien Thevenon, Ariane Soldatos, et al.
Epilepsia|December 6, 2020
FBXO28 causes developmental and epileptic encephalopathy with profound intellectual disabilityAmy L Schneider, Candace T Myers, Alison M Muir, et al.
Lancet (London, England)|August 15, 2017
Intrathecal 2-hydroxypropyl-β-cyclodextrin decreases neurological disease progression in Niemann-Pick disease, type C1: a non-randomised, open-label, phase 1-2 trialDaniel S Ory, Elizabeth A Ottinger, Nicole Yanjanin Farhat, et al.
Frontiers in Immunology|January 31, 2022
The Spectrum of the Deficiency of Adenosine Deaminase 2: An Observational Analysis of a 60 Patient CohortKaryl S Barron, Ivona Aksentijevich, Natalie T Deuitch, et al.
NPJ Precision Oncology|August 14, 2025
A review of diffuse hemispheric glioma, H3 G34-mutant disease development, DNA repair, microenvironment, and treatments on the horizonCameron Crowell, Ziwen Zhu, Yingxiang Li, et al.
Brain : a Journal of Neurology|October 1, 2022
Genomic analysis, immunomodulation and deep phenotyping of patients with nodding syndromeAriane Soldatos, Thomas B Nutman, Tory Johnson, et al.
JAMA Neurology|May 1, 2018
Chronic Meningitis Investigated via Metagenomic Next-Generation SequencingMichael R Wilson, Brian D O'Donovan, Jeffrey M Gelfand, et al.
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