Works by Dermaut, Bart

Results: 51

Mutations other than null mutations producing a pathogenic loss of progranulin in frontotemporal dementia.

Published in:

Human Mutation, 2007, v. 28, n. 4, p. 416, doi. 10.1002/humu.9484

By:

van der Zee, Julie;
Le Ber, Isabelle;
Maurer-Stroh, Sebastian;
Engelborghs, Sebastiaan;
Gijselinck, Ilse;
Camuzat, Agnès;
Brouwers, Nathalie;
Vandenberghe, Rik;
Sleegers, Kristel;
Hannequin, Didier;
Dermaut, Bart;
Schymkowitz, Joost;
Campion, Dominique;
Santens, Patrick;
Martin, Jean-Jacques;
Lacomblez, Lucette;
De Pooter, Tim;
Peeters, Karin;
Mattheijssens, Maria;
Vercelletto, Martine

Publication type:

Article

Mean age-of-onset of familial alzheimer disease caused by presenilin mutations correlates with both increased Aβ42 and decreased Aβ40.

Published in:

Human Mutation, 2006, v. 27, n. 7, p. 686, doi. 10.1002/humu.20336

By:

Kumar-Singh, Samir;
Theuns, Jessie;
Van Broeck, Bianca;
Pirici, Daniel;
Vennekens, Krist'l;
Corsmit, Ellen;
Cruts, Marc;
Dermaut, Bart;
Wang, Rong;
Van Broeckhoven, Christine

Publication type:

Article

Digenic progressive external ophthalmoplegia in a sporadic patient: Recessive mutations in POLG and C10orf2/Twinkle (Communicated by Arnold Munnich).

Published in:

Human Mutation, 2003, v. 22, n. 2, p. 175, doi. 10.1002/humu.10246

By:

Gert Van Goethem;
Ann Löfgren;
Bart Dermaut;
Chantal Ceuterick;
Jean-Jacques Martin;
Christine Van Broeckhoven

Publication type:

Article

Digenic progressive external ophthalmoplegia in a sporadic patient: Recessive mutations in POLG and C10orf2/TwinkleCommunicated by Arnold Munnich.

Published in:

Human Mutation, 2003, v. 22, n. 2, p. 175, doi. 10.1002/humu.10246

By:

Gert Van Goethem;
Ann Löfgren;
Bart Dermaut;
Chantal Ceuterick;
Jean?Jacques Martin;
Christine Van Broeckhoven

Publication type:

Article

Polymorphisms in the prion protein gene and in the doppel gene increase susceptibility for Creutzfeldt-Jakob disease.

Published in:

European Journal of Human Genetics, 2004, v. 12, n. 5, p. 389, doi. 10.1038/sj.ejhg.5201161

By:

Croes, Esther A.;
Alizadeh, Behrooz Z.;
Bertoli-Avella, Aida M.;
Rademaker, Tessa;
Vergeer-Drop, Jeannette;
Dermaut, Bart;
Houwing-Duistermaat, Jeanine J.;
Wientjens, Dorothee P. W. M.;
Hofman, Albert;
Van Broeckhoven, Christine;
van Duijn, Cornelia M.

Publication type:

Article

Novel POLG mutations in progressive external ophthalmoplegia mimicking mitochondrial neurogastrointestinal encephalomyopathy.

Published in:

European Journal of Human Genetics, 2003, v. 11, n. 7, p. 547, doi. 10.1038/sj.ejhg.5201002

By:

Van Goethem, Gert;
Schwartz, Marianne;
Lofgren, Ann;
Dermaut, Bart;
Van Broeckhoven, Christine;
Vissing, John

Publication type:

Article

Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions.

Published in:

Nature Genetics, 2001, v. 28, n. 3, p. 211, doi. 10.1038/90034

By:

Van Goethem, Gert;
Dermaut, Bart;
Löfgren, Ann;
Martin, Jean-Jacques;
Van Broeckhoven, Christine

Publication type:

Article

Novel APP mutation V715A associated with presenile Alzheimer’s disease in a German family.

Published in:

Journal of Neurology, 2003, v. 250, n. 11, p. 1374, doi. 10.1007/s00415-003-0182-5

By:

Cruts, Marc;
Dermaut, Bart;
Rademakers, Rosa;
Van den Broeck, Marleen;
Stögbauer, Florian;
Van Broeckhoven, Christine

Publication type:

Article

Familial Creutzfeldt-Jakob disease in a patient carrying both a presenilin 1 missense substitution and a prion protein gene insertion.

Published in:

Journal of Neurology, 2000, v. 247, n. 5, p. 364, doi. 10.1007/s004150050603

By:

Dermaut, Bart;
Cruts, Marc;
Backhovens, Hubert;
Lübcke, Ursula;
Van Everbroeck, Bart;
Sciot, Raf;
Dom, René;
Martin, Jean-Jacques;
Van Broeckhoven, Christine;
Cras, Patrick

Publication type:

Article

Monosomy 22 in a mixed germ cell-sex cord-stromal tumor of the ovary.

Published in:

Genes, Chromosomes & Cancer, 1997, v. 19, n. 3, p. 192, doi. 10.1002/(SICI)1098-2264(199707)19:3<192::AID-GCC9>3.0.CO;2-T

By:

Speleman, Frank;
Dermaut, Bart;
De Potter, Christian R.;
Van Gele, Mireille;
Van Roy, Nadine;
De Paepe, Anne;
Laureys, Geneviève

Publication type:

Article

Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration.

Published in:

Acta Neuropathologica, 2014, v. 128, n. 3, p. 397, doi. 10.1007/s00401-014-1298-7

By:

Zee, Julie;
Langenhove, Tim;
Kovacs, Gabor;
Dillen, Lubina;
Deschamps, William;
Engelborghs, Sebastiaan;
Matěj, Radoslav;
Vandenbulcke, Mathieu;
Sieben, Anne;
Dermaut, Bart;
Smets, Katrien;
Damme, Philip;
Merlin, Céline;
Laureys, Annelies;
Broeck, Marleen;
Mattheijssens, Maria;
Peeters, Karin;
Benussi, Luisa;
Binetti, Giuliano;
Ghidoni, Roberta

Publication type:

Article

The Alzheimer susceptibility gene BIN1 induces isoform-dependent neurotoxicity through early endosome defects.

Published in:

Acta Neuropathologica Communications, 2022, v. 10, n. 1, p. 1, doi. 10.1186/s40478-021-01285-5

By:

Lambert, Erwan;
Saha, Orthis;
Soares Landeira, Bruna;
Melo de Farias, Ana Raquel;
Hermant, Xavier;
Carrier, Arnaud;
Pelletier, Alexandre;
Gadaut, Johanna;
Davoine, Lindsay;
Dupont, Cloé;
Amouyel, Philippe;
Bonnefond, Amélie;
Lafont, Frank;
Abdelfettah, Farida;
Verstreken, Patrik;
Chapuis, Julien;
Barois, Nicolas;
Delahaye, Fabien;
Dermaut, Bart;
Lambert, Jean-Charles

Publication type:

Article

Ring finger protein 213 assembles into a sensor for ISGylated proteins with antimicrobial activity.

Published in:

Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-26061-w

By:

Thery, Fabien;
Martina, Lia;
Asselman, Caroline;
Zhang, Yifeng;
Vessely, Madeleine;
Repo, Heidi;
Sedeyn, Koen;
Moschonas, George D.;
Bredow, Clara;
Teo, Qi Wen;
Zhang, Jingshu;
Leandro, Kevin;
Eggermont, Denzel;
De Sutter, Delphine;
Boucher, Katie;
Hochepied, Tino;
Festjens, Nele;
Callewaert, Nico;
Saelens, Xavier;
Dermaut, Bart

Publication type:

Article

Mitochondrial Genomic Analysis of Late Onset Alzheimer's Disease Reveals Protective Haplogroups H6A1A/H6A1B: The Cache County Study on Memory in Aging.

Published in:

PLoS ONE, 2012, v. 7, n. 9, p. 1, doi. 10.1371/journal.pone.0045134

By:

Ridge, Perry G.;
Maxwell, Taylor J.;
Corcoran, Christopher D.;
Norton, Maria C.;
Tschanz, Joann T.;
O'Brien, Elizabeth;
Kerber, Richard A.;
Cawthon, Richard M.;
Munger, Ronald G.;
Kauwe, John S. K.;
Dermaut, Bart

Publication type:

Article

Loss and gain of Drosophila TDP-43 impair synaptic efficacy and motor control leading to age-related neurodegeneration by loss-of-function phenotypes.

Published in:

Human Molecular Genetics, 2013, v. 22, n. 8, p. 1539, doi. 10.1093/hmg/ddt005

By:

Diaper, Danielle C.;
Adachi, Yoshitsugu;
Sutcliffe, Ben;
Humphrey, Dickon M.;
Elliott, Christopher J.H.;
Stepto, Alan;
Ludlow, Zoe N.;
Vanden Broeck, Lies;
Callaerts, Patrick;
Dermaut, Bart;
Al-Chalabi, Ammar;
Shaw, Christopher E.;
Robinson, Iain M.;
Hirth, Frank

Publication type:

Article

Expanding the TDP-43 Proteinopathy Pathway From Neurons to Muscle: Physiological and Pathophysiological Functions.

Published in:

Frontiers in Neuroscience, 2022, v. 16, p. 1, doi. 10.3389/fnins.2022.815765

By:

Versluys, Lauren;
Ervilha Pereira, Pedro;
Schuermans, Nika;
De Paepe, Boel;
De Bleecker, Jan L.;
Bogaert, Elke;
Dermaut, Bart

Publication type:

Article

Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA).

Published in:

2022

By:

Schuermans, Nika;
Hemelsoet, Dimitri;
Terryn, Wim;
Steyaert, Sanne;
Van Coster, Rudy;
Coucke, Paul J.;
Steyaert, Wouter;
Callewaert, Bert;
Bogaert, Elke;
Verloo, Patrick;
Vanlander, Arnaud V.;
Debackere, Elke;
Ghijsels, Jody;
LeBlanc, Pontus;
Verdin, Hannah;
Naesens, Leslie;
Haerynck, Filomeen;
Callens, Steven;
Dermaut, Bart;
Poppe, Bruce

Publication type:

journal article

A Belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLD.

Published in:

Brain: A Journal of Neurology, 2006, v. 129, n. 4, p. 841, doi. 10.1093/brain/awl029

By:

Julie van der Zee;
Rosa Rademakers;
Sebastiaan Engelborghs;
Ilse Gijselinck;
Veerle Bogaerts;
Rik Vandenberghe;
Patrick Santens;
Jo Caekebeke;
Tim De Pooter;
Karin Peeters;
Ursula Lübke;
Marleen Van den Broeck;
Jean-Jacques Martin;
Marc Cruts;
Peter P. De Deyn;
Christine Van Broeckhoven;
Bart Dermaut

Publication type:

Article

Genetic Testing Has No Place as a Routine Diagnostic Test in Sporadic and Familial Cases of Alzheimer's Disease.

Published in:

Journal of the American Geriatrics Society, 2004, v. 52, n. 12, p. 2110, doi. 10.1111/j.1532-5415.2004.52573.x

By:

Cammen, Tischa J. M. van der;
Croes, Esther A.;
Dermaut, Bart;
Jager, Marie-Claire de;
Cruts, Marc;
van Broeckhoven, Christine;
van Duijn, Cornelia M.

Publication type:

Article

Isoform‐dependent neurotoxicity of the Alzheimer disease risk factor BIN1: Molecular and cell biology/endosomal‐lysosomal dysfunction.

Published in:

Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.039402

By:

Lambert, Erwan;
Abdelfettah, Farida;
Barois, Nicolas;
Vandekerkhove, Dirk;
Hermant, Xavier;
Ayral, Anne‐Marie;
Davoine, Lindsay;
Dupont, Cloe;
Lafont, Frank;
Amouyel, Philippe;
Chapuis, Julien;
Verstreken, Patrik;
Dermaut, Bart;
Lambert, Jean‐Charles;
Dourlen, Pierre

Publication type:

Article

The TNFRSF6 gene is not implicated in familial early-onset Alzheimer's disease.

Published in:

Human Genetics, 2001, v. 108, n. 6, p. 552, doi. 10.1007/s004390100508

By:

Theuns, Jessie;
Feuk, Lars;
Dermaut, Bart;
Del-Favero, Jurgen;
Roks, Gerwin;
Van den Bossche, Dirk;
Corsmit, Ellen;
Van den Broeck, Marleen;
van Duijn, Cornelia M.;
Cruts, Marc;
Brookes, Anthony J.;
Van Broeckhoven, Christine

Publication type:

Article

Tau phosphorylation regulates the interaction between BIN1's SH3 domain and Tau's proline-rich domain.

Published in:

Acta Neuropathologica Communications, 2015, v. 3, n. 1, p. 1, doi. 10.1186/s40478-015-0237-8

By:

Sottejeau, Yoann;
Bretteville, Alexis;
Cantrelle, François-Xavier;
Malmanche, Nicolas;
Demiaute, Florie;
Mendes, Tiago;
Delay, Charlotte;
Alves, Harmony Alves Dos;
Flaig, Amandine;
Davies, Peter;
Dourlen, Pierre;
Dermaut, Bart;
Laporte, Jocelyn;
Amouyel, Philippe;
Lippens, Guy;
Chapuis, Julien;
Landrieu, Isabelle;
Lambert, Jean-Charles

Publication type:

Article

Developmental Expression of 4-Repeat-Tau Induces Neuronal Aneuploidy in Drosophila Tauopathy Models.

Published in:

Scientific Reports, 2017, p. 40764, doi. 10.1038/srep40764

By:

Malmanche, Nicolas;
Dourlen, Pierre;
Gistelinck, Marc;
Demiautte, Florie;
Link, Nichole;
Dupont, Cloé;
Vanden Broeck, Lies;
Werkmeister, Elisabeth;
Amouyel, Philippe;
Bongiovanni, Antonino;
Bauderlique, Hélène;
Moechars, Dieder;
Royou, Anne;
Bellen, Hugo J.;
Lafont, Frank;
Callaerts, Patrick;
Lambert, Jean-Charles;
Dermaut, Bart

Publication type:

Article

Aberrant splicing in the presenilin-1 intron 4 mutation causes presenile Alzheimer's disease by increased ABeta42 secretion.

Published in:

Human Molecular Genetics, 1999, v. 8, n. 8, p. 1529, doi. 10.1093/hmg/8.8.1529

By:

Jonghe, Chris De;
Cruts, Marc;
Rogaeva, Ekaterina A.;
Tysoe, Carolyn;
Singleton, Andrew;
Vanderstichele, Hugo;
Meschino, Wendy;
Dermaut, Bart;
Vanderhoeven, Inge;
Backhovens, Hubert;
Vanmechelen, Eugeen;
Morris, Christopher M.;
Hardy, John;
Rubinsztein, David C.;
St. George-Hyslop, Peter H.;
Van Broeckhoven, Christine

Publication type:

Article

A novel presenilin 1 mutation associated with Pick's disease but not β-amyloid plaques.

Published in:

Annals of Neurology, 2004, v. 55, n. 5, p. 617

By:

Bart Dermaut;
Samir Kumar-Singh;
Sebastian Engelborghs;
Jessie Theuns;
Rosa Rademakers;
Jos Saerens;
Barbara A. Pickut;
Karin Peeters;
Marleen Van Den Broeck;
Krist'l Vennekens;
Stephen Claes;
Marc Cruts;
Patrick Cras;
Jean-Jacques Martin;
Christine Van Broeckhoven

Publication type:

Article

Reply.

Published in:

Annals of Neurology, 2003, v. 54, n. 4, p. 555

By:

Bart Dermaut;
Esther Croes;
Cornelia van Duijn;
Christine Van Broeckhoven

Publication type:

Article

Early cognitive decline is associated with prion protein codon 129 polymorphism.

Published in:

Annals of Neurology, 2003, v. 54, n. 2, p. 275

By:

Esther A. Croes;
Bart Dermaut;
Jeanine J. Houwing-Duistermaat;
Marleen Van den Broeck;
Marc Cruts;
Monique M. B. Breteler;
Albert Hofman;
Christine van Broeckhoven

Publication type:

Article

PRNP Val129 homozygosity increases risk for early-onset Alzheimer's disease.

Published in:

Annals of Neurology, 2003, v. 53, n. 3, p. 409

By:

Bart Dermaut;
Esther A. Croes;
Rosa Rademakers;
Marleen Van Den Broeck;
Marc Cruts;
Albert Hofman;
Cornelia M. Van Duijn;
Christine Van Broeckhoven

Publication type:

Article

ISOFORM-DEPENDENT NEUROTOXICITY OF THE ALZHEIMER DISEASE RISK FACTOR BIN1 IN DROSOPHILA.

Published in:

Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2017, v. 13, p. P972, doi. 10.1016/j.jalz.2017.06.1309

By:

Dourlen, Pierre;
Abdelfettah, Farida;
Dupont, Cloe;
Davoine, Lindsay;
Amouyel, Philippe;
Lambert, Jean-Charles;
Dermaut, Bart

Publication type:

Article

EXPERIMENTAL IN VIVO EVIDENCE FOR TAU-INDUCED ANEUPLOIDY GENERATED DURING BRAIN DEVELOPMENT IN TAUOPATHIES.

Published in:

Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2017, v. 13, p. P1292, doi. 10.1016/j.jalz.2017.06.1954

By:

Garcia-Nuñez, Alejandro;
Malmanche, Nicolas;
Dourlen, Pierre;
Gistelinck, Marck;
Geurs, Sarah;
Reynaert, Marie-Line;
Davoine, Lindsay;
Dupont, Cloe;
Amouyel, Philippe;
Buee, Luc;
Callaerts, Patrick;
Lambert, Jean-Charles;
Voet, Thierry;
Galas, Marie-Christine;
Dermaut, Bart

Publication type:

Article

Molecular characterisation of bridging integrator 1 (BIN1) interaction with tau.

Published in:

Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2014, v. 10, p. P794, doi. 10.1016/j.jalz.2014.05.1546

By:

Sottejeau, Yoann;
Chapuis, Julien;
Bretteville, Alexis;
Cantrelle, François-Xavier;
Malmanche, Nicolas;
Demiautte, Florie;
Dos Santos, Harmony Alves;
Dourlen, Pierre;
Dermaut, Bart;
Amouyel, Philippe;
Lippens, Guy;
Landrieu, Isabelle;
Lambert, Jean-Charles

Publication type:

Article

Genetic complexity in the BIN1 locus

Published in:

2012

By:

Mounier, Anaïs;
Hansmannel, Franck;
Chapuis, Julien;
Gistelinck, Marc;
Van Cauwenberghe, Caroline;
Grenier-Bolay, Benjamin;
Van Broeckhoven, Christine;
Amouyel, Philippe;
Moechars, Diederik;
Dermaut, Bart;
Lambert, Jean-Charles

Publication type:

Abstract

Bridging integrator 1 (BIN1) as a new partner of Tau?

Published in:

2012

By:

Chapuis, Julien;
Hansmannel, Franck;
Mounier, Anais;
Demiautte, Florie;
Grenier-Bolay, Benjamin;
Bellenguez, Céline;
Letronne, Florent;
Ayral, Anne-Marie;
Amouyel, Philippe;
Dermaut, Bart;
Lambert, Jean-Charles

Publication type:

Abstract

TDP-43 neurotoxicity is caused by a failure of steroid receptor–dependent transcriptional program switching in Drosophila

Published in:

2012

By:

Dermaut, Bart;
Broeck, Lies Vanden;
Sanchez, Marina Naval;
Adachi, Yoshitsugu;
Diaper, Danielle;
Kleinberger, Gernot;
Gistelinck, Marc;
Van Broeckhoven, Christine;
Hirth, Frank;
Aerts, Stein;
Callaerts, Patrick

Publication type:

Abstract

Post-GWAS era: BIN1 as a proof of concept

Published in:

2012

By:

Lambert, Jean-Charles;
Chapuis, Julien;
Amouyel, Philippe;
Dermaut, Bart

Publication type:

Abstract

Assessment of BIN1 involvement in the Alzheimer's Disease pathophysiological process

Published in:

2011

By:

Hansmannel, Franck;
Mounier, Anais;
Gistelinck, Marc;
Grenier-Boley, Benjamin;
Maturski, Marie Eve;
Letronne, Florent;
Ayral, Anne-Marie;
Checler, Frederic;
Buée, Luc;
Amouyel, Philippe;
Dermaut, Bart;
Lambert, Jean-Charles

Publication type:

Abstract

P3-395: Mean age-of-onset of familial Alzheimer disease caused by presenilin mutations correlates with both increased Aβ42 and decreased Aβ40

Published in:

2006

By:

Kumar-Singh, Samir;
Theuns, Jessie;
Van Broeck, Bianca;
Pirici, Daniel;
Vennekens, Krist’l;
Corsmit, Ellen;
Cruts, Marc;
Dermaut, Bart;
Wang, Rong;
Van Broeckhoven, Christine

Publication type:

Abstract

P3-149: An ancestral haplotype harbors a highly prevalent mutation for 17q21-linked tau-negative FTLD in Belgium

Published in:

2006

By:

van der Zee, Julie;
Dermaut, Bart;
Rademakers, Rosa;
Engelborghs, Sebastiaan;
Pirici, Daniel;
Vandenberghe, Rik;
Santens, Patrick;
Caekebeke, Jo;
Kumar-Singh, Samir;
Martin, Jean-Jacques;
De Deyn, Peter P.;
Cruts, Marc;
Van Broeckhoven, Christine

Publication type:

Abstract

P3-395: Mean age-of-onset of familial Alzheimer disease caused by presenilin mutations correlates with both increased Aβ42 and decreased Aβ40

Published in:

2006

By:

Kumar-Singh, Samir;
Theuns, Jessie;
Van Broeck, Bianca;
Pirici, Daniel;
Vennekens, Krist’l;
Corsmit, Ellen;
Cruts, Marc;
Dermaut, Bart;
Wang, Rong;
Van Broeckhoven, Christine

Publication type:

Abstract

P3-149: An ancestral haplotype harbors a highly prevalent mutation for 17q21-linked tau-negative FTLD in Belgium

Published in:

2006

By:

van der Zee, Julie;
Dermaut, Bart;
Rademakers, Rosa;
Engelborghs, Sebastiaan;
Pirici, Daniel;
Vandenberghe, Rik;
Santens, Patrick;
Caekebeke, Jo;
Kumar-Singh, Samir;
Martin, Jean-Jacques;
De Deyn, Peter P.;
Cruts, Marc;
Van Broeckhoven, Christine

Publication type:

Abstract

CHMP2B C-truncating mutations in frontotemporal lobar degeneration are associated with an aberrant endosomal phenotype in vitro.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 2, p. 313, doi. 10.1093/hmg/ddm309

By:

van der Zee, Julie;
Urwin, Hazel;
Engelborghs, Sebastiaan;
Bruyland, Marc;
Vandenberghe, Rik;
Dermaut, Bart;
De Pooter, Tim;
Peeters, Karin;
Santens, Patrick;
De Deyn, Peter P.;
Fisher, Elizabeth M.;
Collinge, John;
Isaacs, Adrian M.;
Van Broeckhoven, Christine

Publication type:

Article

Genomic architecture of human 17q21 linked to frontotemporal dementia uncovers a highly homologous family of low-copy repeats in the tau region.

Published in:

Human Molecular Genetics, 2005, v. 14, n. 13, p. 1753, doi. 10.1093/hmg/ddi182

By:

Cruts, Marc;
Rademakers, Rosa;
Gijselinck, Ilse;
van der Zee, Julie;
Dermaut, Bart;
de Pooter, Tim;
de Rijk, Peter;
Del-Favero, Jurgen;
van Broeckhoven, Christine

Publication type:

Article

Amyloid-β<sub>1–43</sub> cerebrospinal fluid levels and the interpretation of APP, PSEN1 and PSEN2 mutations.

Published in:

Alzheimer's Research & Therapy, 2020, v. 12, n. 1, p. N.PAG, doi. 10.1186/s13195-020-00676-5

By:

Perrone, Federica;
Bjerke, Maria;
Hens, Elisabeth;
Sieben, Anne;
Timmers, Maarten;
De Roeck, Arne;
Vandenberghe, Rik;
Sleegers, Kristel;
Martin, Jean-Jacques;
De Deyn, Peter P.;
Engelborghs, Sebastiaan;
van der Zee, Julie;
Van Broeckhoven, Christine;
Cacace, Rita;
on behalf of the BELNEU Consortium;
Goeman, Johan;
Crols, Roeland;
Dermaut, Bart;
Ivanoiu, Adrian;
Hanseeuw, Bernard

Publication type:

Article

Drosophila Models of Tauopathies: What Have We Learned?

Published in:

2012

By:

Gistelinck, Marc;
Lambert, Jean-Charles;
Callaerts, Patrick;
Dermaut, Bart;
Dourlen, Pierre

Publication type:

Journal Article

Drosophila Models of Tauopathies: What Have We Learned?

Published in:

International Journal of Alzheimer's Disease, 2012, p. 1, doi. 10.1155/2012/970980

By:

Gistelinck, Marc;
Lambert, Jean-Charles;
Callaerts, Patrick;
Dermaut, Bart;
Dourlen, Pierre

Publication type:

Article

Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21.

Published in:

Nature, 2006, v. 442, n. 7105, p. 920, doi. 10.1038/nature05017

By:

Cruts, Marc;
Gijselinck, Ilse;
van der Zee, Julie;
Engelborghs, Sebastiaan;
Wils, Hans;
Pirici, Daniel;
Rademakers, Rosa;
Vandenberghe, Rik;
Dermaut, Bart;
Martin, Jean-Jacques;
van Duijn, Cornelia;
Peeters, Karin;
Sciot, Raf;
Santens, Patrick;
De Pooter, Tim;
Mattheijssens, Maria;
Van den Broeck, Marleen;
Cuijt, Ivy;
Vennekens, Krist'l;
De Deyn, Peter P.

Publication type:

Article

Adult-onset congenital central hypoventilation syndrome due to PHOX2B mutation.

Published in:

Acta Neurologica Belgica, 2021, v. 121, n. 1, p. 23, doi. 10.1007/s13760-020-01363-w

By:

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Pooled analysis of patients with inherited prion disease caused by two- to twelve-octapeptide repeat insertions in the prion protein gene (PRNP).

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