X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (220) 220
Publication (16) 16
Book / eBook (9) 9
Book Review (7) 7
Book Chapter (2) 2
Conference Proceeding (1) 1
Patent (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (113) 113
humans (99) 99
female (74) 74
male (65) 65
neurosciences (62) 62
aged (57) 57
alzheimer's disease (55) 55
alzheimer disease - genetics (47) 47
middle aged (47) 47
aged, 80 and over (34) 34
dementia (33) 33
clinical neurology (31) 31
genetic aspects (28) 28
genotype (27) 27
adult (23) 23
analysis (23) 23
italy (23) 23
mutation (22) 22
risk factors (22) 22
apolipoprotein e (20) 20
gene frequency (20) 20
genetics (20) 20
frontotemporal dementia (19) 19
neurology (18) 18
animals (17) 17
case-control studies (16) 16
genes (16) 16
alleles (15) 15
genetic predisposition to disease (15) 15
age of onset (14) 14
apolipoproteins e - genetics (14) 14
association (14) 14
polymorphism (14) 14
psychiatry (14) 14
geriatrics & gerontology (13) 13
polymorphism, single nucleotide (13) 13
research (13) 13
risk (13) 13
alzheimer’s disease (12) 12
dementia disorders (12) 12
physiological aspects (12) 12
polymorphism, genetic (12) 12
biochemistry & molecular biology (11) 11
cell biology (11) 11
disease (11) 11
genetics & heredity (11) 11
mice (11) 11
mutation - genetics (11) 11
mutations (11) 11
abridged index medicus (10) 10
apolipoprotein e4 - genetics (10) 10
brain (10) 10
cohort studies (10) 10
frontotemporal dementia - genetics (10) 10
gene (10) 10
genetic research (10) 10
pathology (10) 10
allele (9) 9
chemistry, organic (9) 9
further section (9) 9
internal medicine (9) 9
patients (9) 9
alzheimer disease - epidemiology (8) 8
alzheimers-disease (8) 8
amyotrophic-lateral-sclerosis (8) 8
apoe (8) 8
apolipoprotein-e (8) 8
apolipoproteins (8) 8
development and progression (8) 8
diagnosis (8) 8
dna mutational analysis (8) 8
frontotemporal lobar degeneration (8) 8
frontotemporal lobar degeneration - genetics (8) 8
genetic predisposition to disease - genetics (8) 8
genetic variation (8) 8
italy - epidemiology (8) 8
neuropsychological tests (8) 8
oxidative stress (8) 8
amyloid beta-protein precursor - genetics (7) 7
amyloid precursor protein (7) 7
disease progression (7) 7
haplotypes (7) 7
medicine & public health (7) 7
mental disorders (7) 7
oxygen-induced retinopathy (7) 7
parkinsons-disease (7) 7
pathogenesis (7) 7
research article (7) 7
alzheimer disease - pathology (6) 6
amyloid beta-peptides - metabolism (6) 6
amyotrophic lateral sclerosis (6) 6
cells, cultured (6) 6
diagnostic-criteria (6) 6
genetic association studies (6) 6
health aspects (6) 6
immunology (6) 6
medicine and health sciences (6) 6
metaanalysis (6) 6
mouse model (6) 6
pediatrics (6) 6
more...
Library Location Library Location
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Proceedings of the National Academy of Sciences, ISSN 0027-8424, 03/2015, Volume 112, Issue 12, pp. 3680 - 3685
Journal Article
by van der Zee, Julie and Gijselinck, Ilse and Dillen, Lubina and Van Langenhove, Tim and Theuns, Jessie and Engelborghs, Sebastiaan and Philtjens, Stéphanie and Vandenbulcke, Mathieu and Sleegers, Kristel and Sieben, Anne and Bäumer, Veerle and Maes, Githa and Corsmit, Ellen and Borroni, Barbara and Padovani, Alessandro and Archetti, Silvana and Perneczky, Robert and Diehl‐Schmid, Janine and de Mendonça, Alexandre and Miltenberger‐Miltenyi, Gabriel and Pereira, Sónia and Pimentel, José and Nacmias, Benedetta and Bagnoli, Silvia and Sorbi, Sandro and Graff, Caroline and Chiang, Huei‐Hsin and Westerlund, Marie and Sanchez‐Valle, Raquel and Llado, Albert and Gelpi, Ellen and Santana, Isabel and Almeida, Maria Rosário and Santiago, Beatriz and Frisoni, Giovanni and Zanetti, Orazio and Bonvicini, Cristian and Synofzik, Matthis and Maetzler, Walter and vom Hagen, Jennifer Müller and Schöls, Ludger and Heneka, Michael T and Jessen, Frank and Matej, Radoslav and Parobkova, Eva and Kovacs, Gabor G and Ströbel, Thomas and Sarafov, Stayko and Tournev, Ivailo and Jordanova, Albena and Danek, Adrian and Arzberger, Thomas and Fabrizi, Gian Maria and Testi, Silvia and Salmon, Eric and Santens, Patrick and Martin, Jean‐Jacques and Cras, Patrick and Vandenberghe, Rik and De Deyn, Peter Paul and Cruts, Marc and Van Broeckhoven, Christine and van der Zee, Julie and Gijselinck, Ilse and Dillen, Lubina and Van Langenhove, Tim and Theuns, Jessie and Philtjens, Stéphanie and Sleegers, Kristel and Bäumer, Veerle and Maes, Githa and Corsmit, Ellen and Cruts, Marc and Van Broeckhoven, Christine and van der Zee, Julie and Gijselinck, Ilse and Dillen, Lubina and Van Langenhove, Tim and Philtjens, Stéphanie and Theuns, Jessie and Sleegers, Kristel and Bäumer, Veerle and Maes, Githa and Cruts, Marc and Van Broeckhoven, Christine and Engelborghs, Sebastiaan and De Deyn, Peter P and Cras, Patrick and Engelborghs, Sebastiaan and De Deyn, Peter P and Vandenbulcke, Mathieu and Vandenbulcke, Mathieu and Borroni, Barbara and Padovani, Alessandro and Archetti, Silvana and Perneczky, Robert and Diehl‐Schmid, Janine and Synofzik, Matthis and Maetzler, Walter and Müller vom Hagen, Jennifer and ... and European Early-Onset Dementia EOD and European Early-Onset Dementia Consortium
Human Mutation, ISSN 1059-7794, 02/2013, Volume 34, Issue 2, pp. 363 - 373
Journal Article
by der Zee, Julie and Gijselinck, Ilse and Mossevelde, Sara and Perrone, Federica and Dillen, Lubina and Heeman, Bavo and Bäumer, Veerle and Engelborghs, Sebastiaan and Bleecker, Jan and Baets, Jonathan and Gelpi, Ellen and Rojas‐García, Ricardo and Clarimón, Jordi and Lleó, Alberto and Diehl‐Schmid, Janine and Alexopoulos, Panagiotis and Perneczky, Robert and Synofzik, Matthis and Just, Jennifer and Schöls, Ludger and Graff, Caroline and Thonberg, Håkan and Borroni, Barbara and Padovani, Alessandro and Jordanova, Albena and Sarafov, Stayko and Tournev, Ivailo and Mendonça, Alexandre and Miltenberger‐Miltényi, Gabriel and Simões do Couto, Frederico and Ramirez, Alfredo and Jessen, Frank and Heneka, Michael T and Gómez‐Tortosa, Estrella and Danek, Adrian and Cras, Patrick and Vandenberghe, Rik and Jonghe, Peter and Deyn, Peter P and Sleegers, Kristel and Cruts, Marc and Broeckhoven, Christine and Goeman, Johan and Nuytten, Dirk and Smets, Katrien and Robberecht, Wim and Damme, Philip Van and Bleecker, Jan De and Santens, Patrick and Dermaut, Bart and Versijpt, Jan and Michotte, Alex and Ivanoiu, Adrian and Deryck, Olivier and Bergmans, Bruno and Delbeck, Jean and Bruyland, Marc and Willems, Christiana and Salmon, Eric and Pastor, Pau and Ortega‐Cubero, Sara and Benussi, Luisa and Ghidoni, Roberta and Binetti, Giuliano and Hernández, Isabel and Boada, Mercè and Ruiz, Agustín and Sorbi, Sandro and Nacmias, Benedetta and Bagnoli, Silvia and Sorbi, Sandro and Sanchez‐Valle, Raquel and Llado, Albert and Santana, Isabel and Rosário Almeida, Maria and Frisoni, Giovanni B and Maetzler, Walter and Matej, Radoslav and Fraidakis, Matthew J and Kovacs, Gabor G and Fabrizi, Gian Maria and Testi, Silvia and Belgian Neurology Consortium and European Early-Onset Dementia Cons
Human Mutation, ISSN 1059-7794, 03/2017, Volume 38, Issue 3, pp. 297 - 309
We investigated the mutation spectrum of the TANK‐Binding Kinase 1 ( TBK1 ) gene and its associated phenotypic spectrum by exonic resequencing of TBK1 in a... 
TANK‐Binding Kinase 1 | TBK1 | mutations | FTD | ALS | frontotemporal dementia | amyotrophic lateral sclerosis | NFκB luciferase reporter assay | TANK-Binding Kinase 1 | REPEAT EXPANSION | LOBAR DEGENERATION | C9ORF72 | FAMILIAL ALS | BELGIAN COHORT | NFkB luciferase reporter assay | TDP-43 | DISEASE | GENETICS & HEREDITY | ARGYROPHILIC GRAINS | DIAGNOSTIC-CRITERIA | HEXANUCLEOTIDE REPEAT | Sequence Deletion | Humans | Middle Aged | Amyotrophic Lateral Sclerosis - diagnosis | Male | NF-kappa B - metabolism | Case-Control Studies | Female | Protein-Serine-Threonine Kinases - metabolism | Frontotemporal Dementia - genetics | European Continental Ancestry Group - genetics | Genetic Association Studies | Amyotrophic Lateral Sclerosis - genetics | Protein-Serine-Threonine Kinases - genetics | Frontotemporal Dementia - diagnosis | Phenotype | Alleles | Heterozygote | Aged | Enzyme Activation | Mutation | Frontotemporal Dementia - epidemiology | Amino Acid Substitution | Amyotrophic Lateral Sclerosis - epidemiology | Cohort Studies | RNA | Analysis | Luciferase | Amino acids | Amyotrophic lateral sclerosis | Genetic aspects | Dementia | Proteins | Transcription | Risk groups | mRNA turnover | Nonsense-mediated mRNA decay | Sclerosis | Pathogenicity | Missense mutation | Dementia disorders | Frontotemporal dementia | Age | Index Medicus
Journal Article
by van der Zee, Julie and Van Langenhove, Tim and Kovacs, Gabor G and Dillen, Lubina and Deschamps, William and Engelborghs, Sebastiaan and Matěj, Radoslav and Vandenbulcke, Mathieu and Sieben, Anne and Dermaut, Bart and Smets, Katrien and Van Damme, Philip and Merlin, Céline and Laureys, Annelies and Van Den Broeck, Marleen and Mattheijssens, Maria and Peeters, Karin and Benussi, Luisa and Binetti, Giuliano and Ghidoni, Roberta and Borroni, Barbara and Padovani, Alessandro and Archetti, Silvana and Pastor, Pau and Razquin, Cristina and Ortega-Cubero, Sara and Hernández, Isabel and Boada, Mercè and Ruiz, Agustín and de Mendonça, Alexandre and Miltenberger-Miltényi, Gabriel and do Couto, Frederico Simões and Sorbi, Sandro and Nacmias, Benedetta and Bagnoli, Silvia and Graff, Caroline and Chiang, Huei-Hsin and Thonberg, Håkan and Perneczky, Robert and Diehl-Schmid, Janine and Alexopoulos, Panagiotis and Frisoni, Giovanni B and Bonvicini, Christian and Synofzik, Matthis and Maetzler, Walter and vom Hagen, Jennifer Müller and Schöls, Ludger and Haack, Tobias B and Strom, Tim M and Prokisch, Holger and Dols-Icardo, Oriol and Clarimón, Jordi and Lleó, Alberto and Santana, Isabel and Almeida, Maria Rosário and Santiago, Beatriz and Heneka, Michael T and Jessen, Frank and Ramirez, Alfredo and Sanchez-Valle, Raquel and Llado, Albert and Gelpi, Ellen and Sarafov, Stayko and Tournev, Ivailo and Jordanova, Albena and Parobkova, Eva and Fabrizi, Gian Maria and Testi, Silvia and Salmon, Eric and Ströbel, Thomas and Santens, Patrick and Robberecht, Wim and De Jonghe, Peter and Martin, Jean-Jacques and Cras, Patrick and Vandenberghe, Rik and De Deyn, Peter Paul and Cruts, Marc and Sleegers, Kristel and Van Broeckhoven, Christine
Acta Neuropathologica, ISSN 0001-6322, 9/2014, Volume 128, Issue 3, pp. 397 - 410
Journal Article
by Ferrari, Raffaele, PhD and Hernandez, Dena G, MSc and Nalls, Michael A, PhD and Rohrer, Jonathan D, PhD and Ramasamy, Adaikalavan, PhD and Kwok, John B J, PhD and Dobson-Stone, Carol, PhD and Brooks, William S, MBBS and Schofield, Peter R, Prof and Halliday, Glenda M, Prof and Hodges, John R, Prof and Piguet, Olivier, PhD and Bartley, Lauren, MSc and Thompson, Elizabeth, MD and Haan, Eric, Prof and Hernández, Isabel, MD and Ruiz, Agustín, MD and Boada, Mercè, MD and Borroni, Barbara, MD and Padovani, Alessandro, Prof and Cruchaga, Carlos, PhD and Cairns, Nigel J, Prof and Benussi, Luisa, PhD and Binetti, Giuliano, MD and Ghidoni, Roberta, PhD and Forloni, Gianluigi, PhD and Galimberti, Daniela, PhD and Fenoglio, Chiara, PhD and Serpente, Maria, PhD and Scarpini, Elio, MD and Clarimón, Jordi, PhD and Lleó, Alberto, MD and Blesa, Rafael, MD and Waldö, Maria Landqvist, MD and Nilsson, Karin, PhD and Nilsson, Christer, PhD and Mackenzie, Ian R A, Prof and Hsiung, Ging-Yuek R, MD and Mann, David M A, Prof and Grafman, Jordan, Prof and Morris, Christopher M, PhD and Attems, Johannes, Prof and Griffiths, Timothy D, Prof and McKeith, Ian G, Prof and Thomas, Alan J, Prof and Pietrini, P, Prof and Huey, Edward D, MD and Wassermann, Eric M, MD and Baborie, Atik, MD and Jaros, Evelyn, PhD and Tierney, Michael C, MSc and Pastor, Pau, MD and Razquin, Cristina, PhD and Ortega-Cubero, Sara, MD and Alonso, Elena, BSc and Perneczky, Robert, MD and Diehl-Schmid, Janine, MD and Alexopoulos, Panagiotis, MD and Kurz, Alexander, MD and Rainero, Innocenzo, MD and Rubino, Elisa, MD and Pinessi, Lorenzo, Prof and Rogaeva, Ekaterina, PhD and St George-Hyslop, Peter, MD and Rossi, Giacomina, PhD and Tagliavini, Fabrizio, MD and Giaccone, Giorgio, MD and Rowe, James B, PhD and Schlachetzki, Johannes C M, MD and Uphill, James, BSc and Collinge, John, Prof and Mead, Simon, Prof and Danek, Adrian, MD and Van Deerlin, Vivianna M, PhD and Grossman, Murray, Prof and Trojanowski, John Q, Prof and van der Zee, Julie, PhD and Deschamps, William, MSc and Van Langenhove, Tim, MD and Cruts, Marc, PhD and Van Broeckhoven, Christine, Prof and Cappa, Stefano F, Prof and Le Ber, Isabelle, MD and Hannequin, Didier, Prof and Golfier, Véronique, MD and Vercelletto, Martine, MD and Brice, Alexis, MD and Nacmias, Benedetta, PhD and Sorbi, Sandro, Prof and Bagnoli, Silvia, PhD and Piaceri, Irene, PhD and Nielsen, Jørgen E, MD and Hjermind, Lena E, MD and Riemenschneider, Matthias, Prof and Mayhaus, Manuel, PhD and Ibach, Bernd, PhD and Gasparoni, Gilles, PhD and Pichler, Sabrina, MSc and Gu, Wei, PhD and Rossor, Martin N, Prof and ... and Lund University and Psychiatry (Lund) and MultiPark: Multidisciplinary research focused on Parkinson´s disease and Psykiatri, Lund and Lunds universitet
Lancet Neurology, The, ISSN 1474-4422, 2014, Volume 13, Issue 7, pp. 686 - 699
Journal Article
Journal of Alzheimer's Disease, ISSN 1387-2877, 03/2018, Volume 62, Issue 3, pp. 903 - 911
Studies on the genetics of Alzheimer’s disease (AD) have revealed the complexity and heterogeneity of the disease. All our studies have supported this evidence... 
Heterogeneity | Genetics | Partnerships | Alzheimer's disease
Journal Article
Journal of Cutaneous Pathology, ISSN 0303-6987, 06/2019, Volume 46, Issue 6, pp. 447 - 451
Intravascular large B‐cell lymphoma (IVLBCL) is one of the rarest B‐cell non‐Hodgkin lymphomas (NHL), with an aggressive clinical behavior and a poor... 
RECEPTOR | DLBCL | MANAGEMENT | PATHOLOGY | CLINICAL PRESENTATION | DERMATOLOGY | Lymphomas | Biological products | Chemotherapy | CD30 antigen | Aggressive behavior | Lymphocytes B | Medical prognosis | Central nervous system | Lymphoid tissue | Lymphoma | Tumors | Hemopoiesis
Journal Article
by Gagliardi, Luigi and Rusconi, Franca and Bellù, Roberto and Zanini, Rinaldo and Mirri, Gianpaolo and Condò, Manuela and Turoli, Daniela and Vanzati, Mara and Mosca, Fabio and De Nisi, Giuseppe and Polacco, Paola and Villa, Elena and Barbarini, Mario and Fasolato, Valeria and Franco, Caterina and Contiero, Raffaella and Ellero, Serena and Cattarossi, Luigi and Abbiati, Laura and Borroni, Cesarina and Prandi, Giovanna and Fabris, Claudio and Vielmi, Francesca and Borgione, Silvia and Agosti, Massimo and Tandoi, Francesco and Guidali, Rosanna and De Curtis, Mario and Tozzi, Claudio and Lucchini, Renato and Battaglioli, Marina and Lista, Gian Luca and Introvini, Paola and Ferrari, Fabrizio and Gallo, Claudio and Bellante, Elvira and Bottura, Chiara and Zeringyte, Aurelija and Pasquali, Francesca and Boccacci, Simona and Latini, Giuseppe and Giannuzzi, Raffaella and Martinelli, Stefano and Brunelli, Alberto and Di Nunzio, Maria Lucia and Vendemmiati, Antonio and Carli, Giovanna and Bordigato, Michela Alfiero and Filippone, Marco and Meneghesso, Davide and Romeo, Nicola and Mammoliti, Palma and Mastretta, Emanuele and Barberis, Laura and Farina, Daniele and Gancia, Gianpaolo and Dalmazzo, Cristina and Napolitano, Marcello and Messina, Francesco and Villa Betania, Napoli and Magaldi, Rosario and Rinaldi, Matteo and Litta, Rosangela and Lago, Paola and Zanardo, Vincenzo and Chiandetti, Lino and Visentin, Stefano and Presta, Giuseppe and Cella, Davide and Poggiani, Carlo and Ferrari, Daniela and Parati, Sara and Lombardo, Francesco and Grigorio, Rosetta and Barera, Graziano and Bove, Maddalena and Poloniato, Antonella and Burgio, Giampiero and Sala, Elena and Barberi, Ignazio and Tiralongo, Venera and Arco, Alessandro and Mazzeo, Danila and Dani, Carlo and Pratesi, Simone and Mignatti, Valeria and Ancora, Gina and Faldella, Giacomo and Grandi, Sara and Locatelli, Chiara and Stronati, Mauro and Perotti, Gianfranco and Chirico, Gaetano and Migliori, Claudio and De Marini, Sergio and Forleo, Vincenzo and Paludetto, Roberto and Capasso, Letizia and Mansi, Giuseppina and Raimondi, Francesco and ... and Italian Neonatal Network and the Italian Neonatal Network
Pediatrics, ISSN 0031-4005, 2014, Volume 134, Issue 1, pp. e154 - e161
Journal Article
Journal of Neurology, Neurosurgery and Psychiatry, ISSN 0022-3050, 09/2018, Volume 89, Issue Suppl 1, p. A66
Objective The protocol for genetic test in at-risk individuals for Huntington Disease provides a neurological examination and a psychiatric evaluation before... 
Decision making | Counseling
Journal Article