PCR detection of the frequent Taql RFLP at locus D21S13E

Por Stinissen, Piet, Van Broeckhoven, Christine
Publicado em 1991

Pathological mechanisms underlying TDP-43 driven neurodegeneration in FTLD–ALS spectrum disorders

Por Janssens, Jonathan, Van Broeckhoven, Christine
Publicado em 2013

A high frequency EcoRI RFLP detected at the D21S13 locus

Por Stinissen, Piet, Vandenberghe, Antoon, Van Broeckhoven, Christine
Publicado em 1990

PCR detection of two RFLP's at the D21S13 locus

Por Stinissen, Piet, Vandenberghe, Antoon, Van Broeckhoven, Christine
Publicado em 1990

Current status on Alzheimer disease molecular genetics: from past, to present, to future

Por Bettens, Karolien, Sleegers, Kristel, Van Broeckhoven, Christine
Publicado em 2010

TMEM106B a Novel Risk Factor for Frontotemporal Lobar Degeneration

Por van der Zee, Julie, Van Broeckhoven, Christine
Publicado em 2011

Locus-Specific Mutation Databases for Neurodegenerative Brain Diseases

Por Cruts, Marc, Theuns, Jessie, Van Broeckhoven, Christine
Publicado em 2012

The genetic landscape of Alzheimer disease: clinical implications and perspectives

Por Van Cauwenberghe, Caroline, Van Broeckhoven, Christine, Sleegers, Kristel
Publicado no Genet Med (2016)

Genetic Etiology of Parkinson Disease Associated with Mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 Genes: A Mutation Update

Por Nuytemans, Karen, Theuns, Jessie, Cruts, Marc, Van Broeckhoven, Christine
Publicado em 2010

Mechanisms of Granulin Deficiency: Lessons from Cellular and Animal Models

Por Kleinberger, Gernot, Capell, Anja, Haass, Christian, Van Broeckhoven, Christine
Publicado em 2012

The molecular basis of the frontotemporal lobar degeneration–amyotrophic lateral sclerosis spectrum

Por van Langenhove, Tim, van der Zee, Julie, van Broeckhoven, Christine
Publicado em 2012

Novel variants of major drug-metabolising enzyme genes in diverse African populations and their predicted functional effects

Por Matimba, Alice, Del-Favero, Jurgen, Van Broeckhoven, Christine, Masimirembwa, Collen
Publicado em 2009

SNPbox: web-based high-throughput primer design from gene to genome

Por Weckx, Stefan, De Rijk, Peter, Van Broeckhoven, Christine, Del-Favero, Jurgen
Publicado em 2004

Twinkle and POLG defects enhance age-dependent accumulation of mutations in the control region of mtDNA

Por Wanrooij, Sjoerd, Luoma, Petri, van Goethem, Gert, van Broeckhoven, Christine, Suomalainen, Anu, Spelbrink, Johannes N.
Publicado em 2004

De Novo Mutations in the Sodium-Channel Gene SCN1A Cause Severe Myoclonic Epilepsy of Infancy

Por Claes, Lieve, Del-Favero, Jurgen, Ceulemans, Berten, Lagae, Lieven, Van Broeckhoven, Christine, De Jonghe, Peter
Publicado em 2001

Tracing Myelin Protein Zero (P0) in vivo by construction of P0-GFP fusion proteins

Por Ekici, Arif B, Oezbey, Sevinc, Fuchs, Christina, Nelis, Eva, Van Broeckhoven, Christine, Schachner, Melitta, Rautenstrauss, Bernd
Publicado em 2002

Genetic Creutzfeldt-Jakob disease mimicking chronic inflammatory demyelinating polyneuropathy

Por Weckhuysen, Dorien, Schrooten, Maarten, Demaerel, Philippe, Van Broeckhoven, Christine, Tousseyn, Thomas, Kovacs, Gabor G., Van Damme, Philip
Publicado no Neurol Neuroimmunol Neuroinflamm (2015)

Genetic Testing Should Not Be Advocated as a Diagnostic Tool in Familial Forms of Dementia

Por Croes, Esther A., Dermaut, Bart, van der Cammen, Tischa J. M., van Broeckhoven, Christine, van Duijn, Cornelia M.
Publicado em 2000

TDP-43 as a possible biomarker for frontotemporal lobar degeneration: a systematic review of existing antibodies

Por Goossens, Joery, Vanmechelen, Eugeen, Trojanowski, John Q, Lee, Virginia MY, Van Broeckhoven, Christine, van der Zee, Julie, Engelborghs, Sebastiaan
Publicado no Acta Neuropathol Commun (2015)

novoSNP, a novel computational tool for sequence variation discovery

Por Weckx, Stefan, Del-Favero, Jurgen, Rademakers, Rosa, Claes, Lieve, Cruts, Marc, De Jonghe, Peter, Van Broeckhoven, Christine, De Rijk, Peter
Publicado em 2005