Works by Van Broeckhoven, Christine

Results: 291

Associating Alzheimer's disease pathology with its cerebrospinal fluid biomarkers.

Published in:

2022

By:

Bridel, Claire;
Somers, Charisse;
Sieben, Anne;
Rozemuller, Annemieke;
Niemantsverdriet, Ellis;
Struyfs, Hanne;
Vermeiren, Yannick;
Broeckhoven, Christine Van;
Deyn, Peter P De;
Bjerke, Maria;
Nagels, Guy;
Teunissen, Charlotte E;
Engelborghs, Sebastiaan;
Van Broeckhoven, Christine;
De Deyn, Peter P

Publication type:

journal article

Mechanisms of Granulin Deficiency: Lessons from Cellular and Animal Models.

Published in:

Molecular Neurobiology, 2013, v. 47, n. 1, p. 337, doi. 10.1007/s12035-012-8380-8

By:

Kleinberger, Gernot;
Capell, Anja;
Haass, Christian;
Van Broeckhoven, Christine

Publication type:

Article

Locus-specific mutation databases for neurodegenerative brain diseases.

Published in:

Human Mutation, 2012, v. 33, n. 9, p. 1340, doi. 10.1002/humu.22117

By:

Cruts, Marc;
Theuns, Jessie;
Van Broeckhoven, Christine

Publication type:

Article

Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update.

Published in:

2010

By:

Nuytemans, Karen;
Theuns, Jessie;
Cruts, Marc;
Van Broeckhoven, Christine

Publication type:

Other

APP and BACE1 miRNA genetic variability has no major role in risk for Alzheimer disease.

Published in:

Human Mutation, 2009, v. 30, n. 8, p. 1207, doi. 10.1002/humu.21027

By:

Bettens, Karolien;
Brouwers, Nathalie;
Engelborghs, Sebastiaan;
Van Miegroet, Helen;
De Deyn, Peter P.;
Theuns, Jessie;
Sleegers, Kristel;
Van Broeckhoven, Christine

Publication type:

Article

Relative contribution of simple mutations vs. copy number variations in five Parkinson disease genes in the Belgian population.

Published in:

Human Mutation, 2009, v. 30, n. 7, p. 1054, doi. 10.1002/humu.21007

By:

Nuytemans, Karen;
Meeus, Bram;
Crosiers, David;
Brouwers, Nathalie;
Goossens, Dirk;
Engelborghs, Sebastiaan;
Pals, Philippe;
Pickut, Barbara;
Van den Broeck, Marleen;
Corsmit, Ellen;
Cras, Patrick;
De Deyn, Peter P.;
Del-Favero, Jurgen;
Van Broeckhoven, Christine;
Theuns, Jessie

Publication type:

Article

No association between CALHM1 and risk for Alzheimer dementia in a Belgian population.

Published in:

Human Mutation, 2009, v. 30, n. 4, p. E570, doi. 10.1002/humu.20990

By:

Sleegers, Kristel;
Brouwers, Nathalie;
Bettens, Karolien;
Engelborghs, Sebastiaan;
van Miegroet, Helen;
De Deyn, Peter P;
Van Broeckhoven, Christine

Publication type:

Article

Common variation in GRB-associated Binding Protein 2 (GAB2) and increased risk for Alzheimer dementia.

Published in:

Human Mutation, 2009, v. 30, n. 2, p. E338, doi. 10.1002/humu.20909

By:

Sleegers, Kristel;
Bettens, Karolien;
Brouwers, Nathalie;
Engelborghs, Sebastiaan;
van Miegroet, Helen;
De Deyn, Peter P;
Van Broeckhoven, Christine

Publication type:

Article

Genetic variability in the mitochondrial serine protease HTRA2 contributes to risk for Parkinson disease.

Published in:

Human Mutation, 2008, v. 29, n. 6, p. 832, doi. 10.1002/humu.20713

By:

Bogaerts, Veerle;
Nuytemans, Karen;
Reumers, Joke;
Pals, Philippe;
Engelborghs, Sebastiaan;
Pickut, Barbara;
Corsmit, Ellen;
Peeters, Karin;
Schymkowitz, Joost;
De Deyn, Peter Paul;
Cras, Patrick;
Rousseau, Frederic;
Theuns, Jessie;
Van Broeckhoven, Christine

Publication type:

Article

SORL1 is genetically associated with increased risk for late-onset Alzheimer disease in the Belgian population.

Published in:

Human Mutation, 2008, v. 29, n. 5, p. 769, doi. 10.1002/humu.20725

By:

Bettens, Karolien;
Brouwers, Nathalie;
Engelborghs, Sebastiaan;
De Deyn, Peter P.;
Van Broeckhoven, Christine;
Sleegers, Kristel

Publication type:

Article

Genetic variant in the HSPB1 promoter region impairs the HSP27 stress response.

Published in:

Human Mutation, 2007, v. 28, n. 8, p. 830, doi. 10.1002/humu.9503

By:

Dierick, Ines;
Irobi, Joy;
Janssens, Sophie;
Theuns, Jessie;
Lemmens, Robin;
Jacobs, An;
Corsmit, Ellen;
Hersmus, Nicole;
Van Den Bosch, Ludo;
Robberecht, Wim;
De Jonghe, Peter;
Van Broeckhoven, Christine;
Timmerman, Vincent

Publication type:

Article

Visualization of MAPT inversion on stretched chromosomes of tau-negative frontotemporal dementia patients.

Published in:

Human Mutation, 2006, v. 27, n. 10, p. 1057, doi. 10.1002/humu.20391

By:

Gijselinck, Ilse;
Bogaerts, Veerle;
Rademakers, Rosa;
van der Zee, Julie;
Van Broeckhoven, Christine;
Cruts, Marc

Publication type:

Article

Major affective disorders and schizophrenia: a common molecular signature?

Published in:

Human Mutation, 2006, v. 27, n. 9, p. 833, doi. 10.1002/humu.20369

By:

Bogaert, Ann Van Den;
Del-Favero, Jurgen;
Broeckhoven, Christine Van

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

Genes and loci involved in febrile seizures and related epilepsy syndromes.

Published in:

Human Mutation, 2006, v. 27, n. 5, p. 391, doi. 10.1002/humu.20279

By:

Audenaert, Dominique;
Van Broeckhoven, Christine;
De Jonghe, Peter

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

De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancy(Communicated by Jacques S. Beckmann).

Published in:

Human Mutation, 2003, v. 21, n. 6, p. 615, doi. 10.1002/humu.10217

By:

Lieve Claes;
Berten Ceulemans;
Dominique Audenaert;
Katrien Smets;
Ann Löfgren;
Jurgen Del-Favero;
Sirpa Ala-Mello;
Lina Basel-Vanagaite;
Barbara Plecko;
Salmo Raskin;
Paul Thiry;
Nicole I. Wolf;
Christine Van Broeckhoven

Publication type:

Article

Identification of a Drosophila Presenilin Homologue: Evidence of Alternatively Spliced Forms.

Published in:

Journal of Neurogenetics, 1998, v. 12, n. 1, p. 41, doi. 10.3109/01677069809108554

By:

Marfany, Gemma;
Del-Favero, Jurgen;
Valero, Rebeca;
Jonghe, Chris De;
Woodrow, Sarah;
Hendriks, Lydia;
Broeckhoven, Christine Van;
Gonzàlez-Duarte, Roser

Publication type:

Article

A Multicenter Study of Glucocerebrosidase Mutations in Dementia With Lewy Bodies.

Published in:

JAMA Neurology, 2013, v. 70, n. 6, p. 727, doi. 10.1001/jamaneurol.2013.1925

By:

Nalls, Michael A.;
Duran, Raquel;
Lopez, Grisel;
Kurzawa-Akanbi, Marzena;
McKeith, Ian G.;
Chinnery, Patrick F.;
Morris, Christopher M.;
Theuns, Jessie;
Crosiers, David;
Cras, Patrick;
Engelborghs, Sebastiaan;
De Deyn, Peter Paul;
Van Broeckhoven, Christine;
Mann, David M. A.;
Snowden, Julie;
Pickering-Brown, Stuart;
Halliwell, Nicola;
Davidson, Yvonne;
Gibbons, Linda;
Harris, Jenny

Publication type:

Article

Rapidly progressive frontotemporal dementia and bulbar amyotrophic lateral sclerosis in Portuguese patients with C9orf72 mutation.

Published in:

Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration, 2013, v. 14, n. 1, p. 70, doi. 10.3109/17482968.2012.690418

By:

Chester, Catarina;
de Carvalho, Mamede;
Miltenberger, Gabriel;
Pereira, Sónia;
Dillen, Lubina;
van der Zee, Julie;
van Broeckhoven, Christine;
de Mendonça, Alexandre

Publication type:

Article

Founder mutation p.R1441C in the leucine-rich repeat kinase 2 gene in Belgian Parkinson's disease patients.

Published in:

European Journal of Human Genetics, 2008, v. 16, n. 4, p. 471, doi. 10.1038/sj.ejhg.5201986

By:

Nuytemans, Karen;
Rademakers, Rosa;
Theuns, Jessie;
Pals, Philippe;
Engelborghs, Sebastiaan;
Pickut, Barbara;
de Pooter, Tim;
Peeters, Karin;
Mattheijssens, Maria;
Van den Broeck, Marleen;
Cras, Patrick;
De Deyn, Peter Paul;
van Broeckhoven, Christine

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

Parametric and nonparametric genome scan analyses for human handedness.

Published in:

European Journal of Human Genetics, 2003, v. 11, n. 10, p. 779, doi. 10.1038/sj.ejhg.5201048

By:

Agtmael, Tom Van;
Forrest, Susan M.;
Del-Favero, Jurgen;
Van Broeckhoven, Christine;
Williamson, Robert

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

European combined analysis of the CTG18.1 and the ERDA1 CAG/CTG repeats in bipolar disorder.

Published in:

European Journal of Human Genetics, 2002, v. 10, n. 4, p. 276, doi. 10.1038/sj.ejhg.5200803

By:

Del-Favero, Jurgen;
Van Gestel, Sofie;
Borglum, Anders D.;
Muir, Walter;
Ewald, Henrik;
Mors, Ole;
Ivezic, Sladana;
Oruc, Lilijana;
Adolfsson, Rolf;
Blackwood, Douglas;
Kruse, Torben;
Mendlewicz, Julien;
Schalling, Martin;
Van Broeckhoven, Christine

Publication type:

Article

A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2F) maps to chromosome 7q11-q21.

Published in:

European Journal of Human Genetics, 2001, v. 9, n. 8, p. 646, doi. 10.1038/sj.ejhg.5200686

By:

Ismailov, Shoukhrat M;
Fedotov, Valeriy P;
Dadali, Elena L;
Polyakov, Alexander V;
Van Broeckhoven, Christine;
Ivanov, Vladimir I;
De Jonghe, Peter;
Timmerman, Vincent;
Evgrafov, Oleg V

Publication type:

Article

No evidence for the involvement of CAG/CTG repeats from within 18q21.33–q23 in bipolar disorder.

Published in:

European Journal of Human Genetics, 2000, v. 8, n. 5, p. 385, doi. 10.1038/sj.ejhg.5200469

By:

Goossens, Dirk;
Villafuerte, Sandra;
Tissir, Fadel;
Van Gestel, Sofie;
Claes, Stephan;
Souery, Daniel;
Massat, Isabelle;
Van den Bossche, Dirk;
Van Zand, Karel;
Mendlewicz, Julien;
Van Broeckhoven, Christine;
Del-Favero, Jurgen

Publication type:

Article

Genetic refinement of the hereditary neuralgic amyotrophy (HNA) locus at chromosome 17q25.

Published in:

European Journal of Human Genetics, 1999, v. 7, n. 8, p. 920, doi. 10.1038/sj.ejhg.5200384

By:

Meuleman, Jan;
Kuhlenbäumer, Gregor;
Schirmacher, Anja;
Wehnert, Manfred;
De Jonghe, Peter;
De Vriendt, Els;
Young, Peter;
Airaksinen, Eila;
Pou-Serradell, Adolfo;
Prats, José-Maria;
Ringelstein, Bernd;
Stögbauer, Florian;
Van Broeckhoven, Christine;
Timmerman, Vincent

Publication type:

Article

Genetic association of the presenilin-1 regulatory region with early-onset Alzheimer's disease in a population-based sample.

Published in:

European Journal of Human Genetics, 1999, v. 7, n. 7, p. 801, doi. 10.1038/sj.ejhg.5200373

By:

Duijn, Cornelia M van;
Cruts, Marc;
Theuns, Jessie;
Van Gassen, Geert;
Backhovens, Hubert;
van den Broeck, Marleen;
Wehnert, Anita;
Serneels, Sally;
Hofman, Albert;
Van Broeckhoven, Christine

Publication type:

Article

Genetic refinement and physical mapping of a chromosome 18q candidate region for bipolar disorder.

Published in:

European Journal of Human Genetics, 1999, v. 7, n. 4, p. 427, doi. 10.1038/sj.ejhg.5200318

By:

Verheyen, Geert R;
Villafuerte, Sandra M;
Del-Favero, Jurgen;
Souery, Daniel;
Mendlewicz, Julien;
Van Broeckhoven, Christine;
Raeymaekers, Peter

Publication type:

Article

Phenotypic Variation of Autosomal-Dominant Corticobasal Degeneration.

Published in:

European Neurology, 2012, v. 67, n. 3, p. 142, doi. 10.1159/000334731

By:

Jung, Hans H.;
Bremer, Juliane;
Streffer, Johannes;
Virdee, Kanwar;
Spillantini, Maria Grazia;
Crowther, R. Anthony;
Brugger, Peter;
Van Broeckhoven, Christine;
Aguzzi, Adriano;
Tolnay, Markus

Publication type:

Article

Peripheral myelin protein 2 - a novel cluster of mutations causing Charcot-Marie-Tooth neuropathy.

Published in:

2019

By:

Palaima, Paulius;
Chamova, Teodora;
Jander, Sebastian;
Mitev, Vanyo;
Van Broeckhoven, Christine;
Tournev, Ivailo;
Peeters, Kristien;
Jordanova, Albena

Publication type:

journal article

Frontotemporal Lobar Degeneration: Current Concepts in the Light of Recent Advances.

Published in:

Brain Pathology, 2007, v. 17, n. 1, p. 104, doi. 10.1111/j.1750-3639.2007.00055.x

By:

Kumar-Singh, Samir;
Van Broeckhoven, Christine

Publication type:

Article

The future of genetic research on neurodegeneration.

Published in:

2010

By:

Van Broeckhoven, Christine

Publication type:

Opinion

Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis.

Published in:

Nature Genetics, 2008, v. 40, n. 12, p. 1402, doi. 10.1038/ng.251

By:

Aulchenko, Yurii S.;
Hoppenbrouwers, Ilse A.;
Ramagopalan, Sreeram V.;
Broer, Linda;
Jafari, Naghmeh;
Hillert, Jan;
Link, Jenny;
Lundström, Wangko;
Greiner, Eva;
Dessa Sadovnick, A;
Goossens, Dirk;
Van Broeckhoven, Christine;
Del-Favero, Jurgen;
Ebers, George C.;
Oostra, Ben A.;
van Duijn, Cornelia M.;
Hintzen, Rogier Q.

Publication type:

Article

Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis.

Published in:

Nature Genetics, 2008, v. 40, n. 1, p. 29, doi. 10.1038/ng.2007.52

By:

van Es, Michael A.;
van Vught, Paul W. J.;
Blauw, Hylke M.;
Franke, Lude;
Saris, Christiaan G. J.;
Van Den Bosch, Ludo;
de Jong, Sonja W.;
de Jong, Vianney;
Baas, Frank;
van't Slot, Ruben;
Lemmens, Robin;
Schelhaas, Helenius J.;
Birve, Anna;
Sleegers, Kristel;
Van Broeckhoven, Christine;
Schymick, Jennifer C.;
Traynor, Bryan J.;
Wokke, John H. J.;
Wijmenga, Cisca;
Robberecht, Wim

Publication type:

Article

Hot-spot residue in small heat-shock protein 22 causes distal motor neuropathy.

Published in:

Nature Genetics, 2004, v. 36, n. 6, p. 597, doi. 10.1038/ng1328

By:

Irobi, Joy;
Van Impe, Katrien;
Seeman, Pavel;
Jordanova, Albena;
Dierick, Ines;
Verpoorten, Nathalie;
Michalik, Andrej;
De Vriendt, Els;
Jacobs, An;
Van Gerwen, Veerle;
Vennekens, Krist'l;
Mazanec, Radim;
Tournev, Ivailo;
Hilton-Jones, David;
Talbot, Kevin;
Kremensky, Ivo;
Van Den Bosch, Ludo;
Robberecht, Wim;
Vandekerckhove, Joël;
Van Broeckhoven, Christine

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

Of giant axons and curly hair.

Published in:

Nature Genetics, 2000, v. 26, n. 3, p. 254, doi. 10.1038/81521

By:

Timmerman, Vincent;
De Jonghe, Peter;
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

Diagnostic accuracy of the Preclinical AD Scale (PAS) in cognitively mildly impaired subjects.

Published in:

Journal of Neurology, 2002, v. 249, n. 3, p. 312, doi. 10.1007/s004150200011

By:

Visser, Pieter Jelle;
Verhey, Frans R. J.;
Scheltens, Philip;
Cruts, Marc;
Ponds, Rudolf W. H. M.;
Van Broeckhoven, Christine L.;
Jolles, Jellemer

Publication type:

Article

Hereditary Neuralgic Amyotrophy (HNA) is genetically heterogeneous.

Published in:

Journal of Neurology, 2001, v. 248, n. 10, p. 861

By:

Kuhlenbäumer, Gregor;
Meuleman, Jan;
De Jonghe, Peter;
Falck, Björn;
Young, Peter;
Hünermund, Gert;
Van Broeckhoven, Christine;
Timmerman, Vincent;
Stögbauer, Florian

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

TMEM106B a Novel Risk Factor for Frontotemporal Lobar Degeneration.

Published in:

Journal of Molecular Neuroscience, 2011, v. 45, n. 3, p. 516, doi. 10.1007/s12031-011-9555-x

By:

van der Zee, Julie;
Van Broeckhoven, Christine

Publication type:

Article

Guanosine triphosphate cyclohydrolase 1 promoter deletion causes dopa-responsive dystonia.

Published in:

Movement Disorders, 2012, v. 27, n. 11, p. 1451, doi. 10.1002/mds.25147

By:

Theuns, Jessie;
Crosiers, David;
Debaene, Luc;
Nuytemans, Karen;
Meeus, Bram;
Sleegers, Kristel;
Goossens, Dirk;
Corsmit, Ellen;
Elinck, Ellen;
Peeters, Karin;
Mattheijssens, Maria;
Pickut, Barbara;
Del-Favero, Jurgen;
Engelborghs, Sebastiaan;
De Deyn, Peter Paul;
Cras, Patrick;
Van Broeckhoven, Christine

Publication type:

Article

Neurodegenerative parkinsonism and progressive external ophthalmoplegia with a Twinkle mutation.

Published in:

Movement Disorders, 2009, v. 24, n. 2, p. 308, doi. 10.1002/mds.22198

By:

Vandenberghe, Wim;
Van Laere, Koen;
Debruyne, Frederik;
Van Broeckhoven, Christine;
Van Goethem, Gert

Publication type:

Article

Bidirectional transcripts of the expanded <i>C9orf72</i> hexanucleotide repeat are translated into aggregating dipeptide repeat proteins.

Published in:

Acta Neuropathologica, 2013, v. 126, n. 6, p. 881, doi. 10.1007/s00401-013-1189-3

By:

Mori, Kohji;
Arzberger, Thomas;
Grässer, Friedrich A.;
Gijselinck, Ilse;
May, Stephanie;
Rentzsch, Kristin;
Weng, Shih-Ming;
Schludi, Martin H.;
van der Zee, Julie;
Cruts, Marc;
Van Broeckhoven, Christine;
Kremmer, Elisabeth;
Kretzschmar, Hans A.;
Haass, Christian;
Edbauer, Dieter

Publication type:

Article

The genetics and neuropathology of frontotemporal lobar degeneration.

Published in:

Acta Neuropathologica, 2012, v. 124, n. 3, p. 353, doi. 10.1007/s00401-012-1029-x

By:

Sieben, Anne;
Van Langenhove, Tim;
Engelborghs, Sebastiaan;
Martin, Jean-Jacques;
Boon, Paul;
Cras, Patrick;
De Deyn, Peter-Paul;
Santens, Patrick;
Van Broeckhoven, Christine;
Cruts, Marc

Publication type:

Article

Cholesterol and Triglycerides Moderate the Effect of Apolipoprotein E on Memory Functioning in Older Adults.

Published in:

Journals of Gerontology Series B: Psychological Sciences & Social Sciences, 2007, v. 62, n. 2, p. 112, doi. 10.1093/geronb/62.2.P112

By:

De Frias, Cindy M.;
Bunce, David;
Wahlin, Åke;
Adolfsson, Rolf;
Sleegers, Kristel;
Cruts, Marc;
Van Broeckhoven, Christine;
Nilsson, Lars-Göran

Publication type:

Article