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Pediatric Research|August 1, 2002
Myelin oligodendrocyte gene polymorphisms and childhood multiple sclerosisAndreas Ohlenbusch, Daniela Pohl, Folker HanefeldJournal of the Neurological Sciences|April 10, 2014
A novel ATP1A3 mutation with unique clinical presentationHendrik Rosewich, Martina Baethmann, Andreas Ohlenbusch, et al.Journal of Pediatric Genetics|February 15, 2018
Cathepsin D Polymorphism C224T in Childhood-Onset Neurodegenerative Disorders: No Impact for Childhood DementiaMatthias Kettwig, Andreas Ohlenbusch, Klaus Jung, et al.American Journal of Medical Genetics. Part A|August 9, 2005
Mutation analysis of the HDAC 1, 2, 8 and CDKL5 genes in Rett syndrome patients without mutations in MECP2Peter Huppke, Andreas Ohlenbusch, Cornelia Brendel, et al.Journal of Alzheimer'S Disease : JAD|February 19, 2016
Late-Onset Metachromatic Leukodystrophy with Early Onset Dementia Associated with a Novel Missense Mutation in the Arylsulfatase A GeneKatharina Stoeck, Marios Nikos Psychogios, Andreas Ohlenbusch, et al.Cognitive and Behavioral Neurology : Official Journal of the Society for Behavioral and Cognitive Neurology|December 19, 2018
Alternating Hemiplegia of Childhood in Two Adult Patients with a Mild SyndromeKatarzyna Ewa Polanowska, Karolina Dzieżyc, Hendrik Rosewich, et al.BMC Medical Genetics|August 18, 2011
Characterization of two common 5' polymorphisms in PEX1 and correlation to survival in PEX1 peroxisome biogenesis disorder patientsSven Thoms, Sabine Grønborg, Jana Rabenau, et al.Oncotarget|February 9, 2018
Splice variants of the endonucleases XPF and XPG contain residual DNA repair capabilities and could be a valuable tool for personalized medicineJanin Lehmann, Steffen Schubert, Christina Seebode, et al.Human Mutation|March 19, 2005
Identification of ten novel mutations in patients with eIF2B-related disordersAndreas Ohlenbusch, Marco Henneke, Knut Brockmann, et al.Photodermatology, Photoimmunology & Photomedicine|July 9, 2016
A unique chromosomal in-frame deletion identified among seven XP-C patientsSteffen Schubert, Petra Rieper, Andreas Ohlenbusch, et al.Pageof 3