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Journal of Neurology|September 9, 2023
Pooled analysis of patients with inherited prion disease caused by two- to twelve-octapeptide repeat insertions in the prion protein gene (PRNP)Astrid Van den Broecke, Alexander Decruyenaere, Nika Schuermans, et al.
The Journal of Cell Biology|July 7, 2005
Aberrant lysosomal carbohydrate storage accompanies endocytic defects and neurodegeneration in Drosophila benchwarmerBart Dermaut, Koenraad K Norga, Artur Kania, et al.
Frontiers in Cellular and Infection Microbiology|November 22, 2021
Proteome Profiling of RNF213 Depleted Cells Reveals Nitric Oxide Regulator DDAH1 Antilisterial ActivityLia Martina, Caroline Asselman, Fabien Thery, et al.
Neurology|April 5, 2015
RNF216 mutations as a novel cause of autosomal recessive Huntington-like disorderPatrick Santens, Tim Van Damme, Wouter Steyaert, et al.
Neurobiology of Aging|December 3, 2014
Functional complementation in Drosophila to predict the pathogenicity of TARDBP variants: evidence for a loss-of-function mechanismLies Vanden Broeck, Gernot Kleinberger, Julien Chapuis, et al.
Cell Reports|July 2, 2014
HDAC6 is a Bruchpilot deacetylase that facilitates neurotransmitter releaseKatarzyna Miskiewicz, Liya E Jose, Wondwossen M Yeshaw, et al.
Neuroscience Letters|October 11, 2005
The UBQLN1 polymorphism, UBQ-8i, at 9q22 is not associated with Alzheimer's disease with onset before 70 yearsNathalie Brouwers, Kristel Sleegers, Sebastiaan Engelborghs, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 1, 2008
Vagus nerve stimulation for refractory status epilepticusVeerle De Herdt, Liesbeth Waterschoot, Kristl Vonck, et al.
Annals of Neurology|February 26, 2003
PRNP Val129 homozygosity increases risk for early-onset Alzheimer's diseaseBart Dermaut, Esther A Croes, Rosa Rademakers, et al.
Human Mutation|June 6, 2006
Mean age-of-onset of familial alzheimer disease caused by presenilin mutations correlates with both increased Abeta42 and decreased Abeta40Samir Kumar-Singh, Jessie Theuns, Bianca Van Broeck, et al.
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