An infantile/juvenile form of Alexander disease caused by a R79H mutation in GFAPInstructions for use Title An infantile/juvenile form of Alexander disease caused by a R79H

Does genetic anticipation occur in familial Alexander disease?Link to publication record in King's Research Portal Citation for published version (APA): Hunt, C. K.,

Shandong Provincial Hospital Jing Yu  Shandong Medical College Shougang Guo  ( [email protected] ) Shandong Provincial Hospital https://orcid.org/0000-0003-0748-6990

GFAP mutations, age at onset, and clinical subtypes in Alexander disease M. Prust, BA J. Wang, PhD H. Morizono, PhD A. Messing, VMD, PhD M. Brenner, PhD E. Gordon, MS T.

Alexander Disease HH 2020 LCN Winter MeetingSpeakers Alexander Disease Children What is Alexander Disease? • Referred to as ALX, AxD, Demyelinogenic Leukodystrophy,

doi:10.1086/504411www.ajhg.org The American Journal of Human Genetics Volume 79 August 2006 197 ARTICLE The Alexander Disease–Causing Glial Fibrillary Acidic Protein

A Novel Mutation of GFAP Causing Adult-Onset Alexander DiseaseFrontiers in Neurology | www.frontiersin.org 1 November 2019 | Volume 10 | Article 1124 Edited by: Neurogenetics,

untitledSERIAL QUANTITATIVE MR IMAGING AND SPECTROSCOPY OF WHITE MATTER J. Patrick van der Voorn Petra J. W. Pouwels Gajja S Salomons Frederik Barkhof Marjo S. van der Knaap

191 Dear Editor, Alexander disease (AD) is a progressive degenerative leukodystrophy, which typically presents in infancy. Neonatal, juvenile and adult-onset forms of AD

untitledvan der Voorn, J.P. document version Publisher's PDF, also known as Version of record Link to publication in VU Research Portal citation for published version