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1. Full Text Frontotemporal dementia and its subtypes: a genome-wide association study
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
Summary Background Frontotemporal dementia (FTD) is a complex disorder characterised by a broad range of clinical manifestations, differential pathological... 
Neurology | GENETIC-VARIATION | COMMON VARIANTS | PROTEIN | LOBAR DEGENERATION | DISEASE | SUSCEPTIBILITY LOCI | RISK | MUTATIONS | HEXANUCLEOTIDE REPEAT | BRAIN | CLINICAL NEUROLOGY | Frontotemporal Dementia - genetics | Humans | Middle Aged | Aged, 80 and over | Adult | Female | Genotype | Male | Aged | Frontotemporal Dementia - diagnosis | Genome-Wide Association Study - methods | Frontotemporal Dementia - classification | Genetic research | Genomics | Dementia | Genealogy | Principal components analysis | Genomes | Patients | Proteins | Studies | Pathology | Semantics | Consent | Quality control | Aging | Aphasia | DNA methylation | Mutation | Genetic testing | Chromosomes | Deoxyribonucleic acid--DNA | Neurologi | Clinical Medicine | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap
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2. Full Text Association between repeat sizes and clinical and pathological characteristics in carriers of C9ORF72 repeat expansions (Xpansize-72): a cross-sectional cohort study
by van Blitterswijk, Marka, PhD and DeJesus-Hernandez, Mariely, BS and Niemantsverdriet, Ellis, BS and Murray, Melissa E, PhD and Heckman, Michael G, MS and Diehl, Nancy N, BS and Brown, Patricia H, MS and Baker, Matthew C, BSc and Finch, NiCole A, MS and Bauer, Peter O, PhD and Serrano, Geidy, PhD and Beach, Thomas G, Prof and Josephs, Keith A, Prof and Knopman, David S, Prof and Petersen, Ronald C, Prof and Boeve, Bradley F, Prof and Graff-Radford, Neill R, Prof and Boylan, Kevin B, MD and Petrucelli, Leonard, Prof and Dickson, Dennis W, Prof and Rademakers, Rosa, Dr
Lancet Neurology, The, ISSN 1474-4422, 2013, Volume 12, Issue 10, pp. 978 - 988
Summary Background Hexanucleotide repeat expansions in chromosome 9 open reading frame 72 ( C9ORF72 ) are the most common known genetic cause of frontotemporal... 
Neurology | Frontotemporal Dementia - genetics | Cross-Sectional Studies | Frontal Lobe - metabolism | Comorbidity | DNA Repeat Expansion - genetics | Cerebellum - metabolism | Humans | Middle Aged | Genotype | Male | Motor Neuron Disease - epidemiology | Cerebellum - pathology | Motor Neuron Disease - pathology | Proteins - genetics | Phenotype | Motor Neuron Disease - genetics | Age of Onset | Female | Aged | C9orf72 Protein | Frontotemporal Dementia - epidemiology | Frontal Lobe - pathology | Cohort Studies | Frontotemporal Dementia - pathology | Neurosciences | Dementia
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3. Full Text Neuroimaging correlates of pathologically defined subtypes of Alzheimer's disease: a case-control study
by Whitwell, Jennifer L, Dr and Dickson, Dennis W, Prof and Murray, Melissa E, PhD and Weigand, Stephen D, MS and Tosakulwong, Nirubol, BS and Senjem, Matthew L, MS and Knopman, David S, Prof and Boeve, Bradley F, Prof and Parisi, Joseph E, Prof and Petersen, Ronald C, Prof and Jack, Clifford R, Prof and Josephs, Keith A, Prof
Lancet Neurology, The, ISSN 1474-4422, 2012, Volume 11, Issue 10, pp. 868 - 877
Summary Background Three subtypes of Alzheimer's disease (AD) have been pathologically defined on the basis of the distribution of neurofibrillary tangles:... 
Neurology | HIPPOCAMPAL VOLUME | DIAGNOSIS | IMAGES | PROGRESSIVE APHASIA | NEUROPATHOLOGY | PRESENTATIONS | ONSET | CLINICAL NEUROLOGY | VOXEL-BASED MORPHOMETRY | Neuroimaging - methods | Alzheimer Disease - classification | Humans | Atrophy - pathology | Magnetic Resonance Imaging - methods | Male | Case-Control Studies | Alzheimer Disease - pathology | Alzheimer Disease - diagnosis | Magnetic Resonance Imaging - instrumentation | Neuroimaging - instrumentation | Aged, 80 and over | Brain - pathology | Female | Aged | Medicine, Experimental | Medical research | Diagnostic imaging | Alzheimer's disease | Analysis
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4. Full Text CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia
by Williams, Kelly L and Topp, Simon and Yang, Shu and Smith, Bradley and Fifita, Jennifer A and Warraich, Sadaf T and Zhang, Katharine Y and Farrawell, Natalie and Vance, Caroline and Hu, Xun and Chesi, Alessandra and Leblond, Claire S and Lee, Albert and Rayner, Stephanie L and Sundaramoorthy, Vinod and Dobson-Stone, Carol and Molloy, Mark P and Van Blitterswijk, Marka and Dickson, Dennis W and Petersen, Ronald C and Graff-Radford, Neill R and Boeve, Bradley F and Murray, Melissa E and Pottier, Cyril and Don, Emily and Winnick, Claire and McCann, Emily P and Hogan, Alison and Daoud, Hussein and Levert, Annie and Dion, Patrick A and Mitsui, Jun and Ishiura, Hiroyuki and Takahashi, Yuji and Goto, Jun and Kost, Jason and Gellera, Cinzia and Gkazi, Athina Soragia and Miller, Jack and Stockton, Joanne and Brooks, William S and Boundy, Karyn and Polak, Meraida and Muñoz-Blanco, José Luis and Esteban-Pérez, Jesús and Rábano, Alberto and Hardiman, Orla and Morrison, Karen E and Ticozzi, Nicola and Silani, Vincenzo and De Belleroche, Jacqueline and Glass, Jonathan D and Kwok, John B.J and Guillemin, Gilles J and Chung, Roger S and Tsuji, Shoji and Brown, Robert H and García-Redondo, Alberto and Rademakers, Rosa and Landers, John E and Gitler, Aaron D and Rouleau, Guy A and Cole, Nicholas J and Yerbury, Justin J and Atkin, Julie D and Shaw, Christopher E and Nicholson, Garth A and Blair, Ian P
Nature Communications, ISSN 2041-1723, 04/2016, Volume 7, Issue 1, p. 11253
Amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) are overlapping, fatal neurodegenerative disorders in which the molecular and pathogenic... 
UBIQUITIN-PROTEASOME SYSTEM | PROTEIN | LOBAR DEGENERATION | GENE | RNA | TDP-43 | MULTIDISCIPLINARY SCIENCES | ALS | FRAMEWORK | STRESS | Frontotemporal Dementia - genetics | Amino Acid Sequence | Genetic Predisposition to Disease - genetics | Genome-Wide Association Study | Amyotrophic Lateral Sclerosis - genetics | Humans | Middle Aged | Cyclins - genetics | Family Health | Male | Chromosome Mapping | Mutation, Missense | Sequence Homology, Amino Acid | Animals | Pedigree | Cell Line, Tumor | Adult | Female | Aged | Sequence Analysis, DNA - methods | Chromosomes, Human, Pair 16 - genetics
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5. Full Text Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting
by Chauhan, Ganesh and Adams, Hieab H.H and Satizabal, Claudia L and Bis, Joshua C and Teumer, Alexander and Sargurupremraj, Muralidharan and Hofer, Edith and Trompet, Stella and Hilal, Saima and Smith, Albert Vernon and Jian, Xueqiu and Malik, Rainer and Traylor, Matthew and Pulit, Sara L and Amouyel, Philippe and Mazoyer, Bernard and Zhu, Yi-Cheng and Kaffashian, Sara and Schilling, Sabrina and Beecham, Gary W and Montine, Thomas J and Schellenberg, Gerard D and Kjartansson, Olafur and Guðnason, Vilmundur and Knopman, David S and Griswold, Michael E and Windham, B Gwen and Gottesman, Rebecca F and Mosley, Thomas H and Schmidt, Reinhold and Saba, Yasaman and Schmidt, Helena and Takeuchi, Fumihiko and Yamaguchi, Shuhei and Nabika, Toru and Kato, Norihiro and Rajan, Kumar B and Aggarwal, Neelum T and De Jager, Philip L and Evans, Denis A and Psaty, Bruce M and Rotter, Jerome I and Rice, Kenneth and Lopez, Oscar L and Liao, Jiemin and Chen, Christopher and Cheng, Ching-Yu and Wong, Tien Y and Ikram, Mohammad K and van der Lee, Sven J and Amin, Najaf and Chouraki, Vincent and DeStefano, Anita L and Aparicio, Hugo J and Romero, Jose R and Maillard, Pauline and DeCarli, Charles and Wardlaw, Joanna M and Hernández, Maria del C Valdés and Luciano, Michelle and Liewald, David and Deary, Ian J and Starr, John M and Bastin, Mark E and Muñoz Maniega, Susana and Slagboom, P Eline and Beekman, Marian and Deelen, Joris and Uh, Hae-Won and Lemmens, Robin and Brodaty, Henry and Wright, Margaret J and Ames, David and Boncoraglio, Giorgio B and Hopewell, Jemma C and Beecham, Ashley H and Blanton, Susan H and Wright, Clinton B and Sacco, Ralph L and Wen, Wei and Thalamuthu, Anbupalam and Armstrong, Nicola J and Chong, Elizabeth and Schofield, Peter R and Kwok, John B and van der Grond, Jeroen and Stott, David J and Ford, Ian and Jukema, J Wouter and Vernooij, Meike W and Hofman, Albert and Uitterlinden, André G and van der Lugt, Aad and Wittfeld, Katharina and Grabe, Hans J and Hosten, Norbert and von Sarnowski, Bettina and Völker, Uwe and Levi, Christopher and Jimenez-Conde, Jordi and ... and Stroke Genetics Network SiGN and CHARGE Consortium and ISGC and METASTROKE and ADGC and Stroke Genetics Network (SiGN), the International Stroke Genetics Consortium (ISGC), METASTROKE, Alzheimer's Disease Genetics Consortium (ADGC), and the Neurology Working Group of the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium and Institutionen för biomedicin and Sahlgrenska akademin and Institute of Biomedicine and Göteborgs universitet and Gothenburg University and Sahlgrenska Academy
Neurology, ISSN 0028-3878, 01/2019, Volume 92, Issue 5, pp. e486 - e503
OBJECTIVETo explore genetic and lifestyle risk factors of MRI-defined brain infarcts (BI) in large population-based cohorts. METHODSWe performed meta-analyses... 
SMALL VESSEL DISEASE | METAANALYSIS | POLYMORPHISMS | MENDELIAN RANDOMIZATION | MATTER HYPERINTENSITY VOLUME | ISCHEMIC-STROKE | BLOOD-PRESSURE | CLINICAL NEUROLOGY | GENOME-WIDE ASSOCIATION | SILENT | INSIGHTS | Neurosciences | silent | metaanalysis | disease | insights | small vessel | matter hyperintensity volume | Neurosciences & Neurology | polymorphisms | genome-wide association | blood-pressure | mendelian randomization | ischemic-stroke | Neurovetenskaper
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6. Full Text Consensus classification of posterior cortical atrophy
by Crutch, Sebastian J and Schott, Jonathan M and Rabinovici, Gil D and Murray, Melissa and Snowden, Julie S and van der Flier, Wiesje M and Dickerson, Bradford C and Vandenberghe, Rik and Ahmed, Samrah and Bak, Thomas H and Boeve, Bradley F and Butler, Christopher and Cappa, Stefano F and Ceccaldi, Mathieu and de Souza, Leonardo Cruz and Dubois, Bruno and Felician, Olivier and Galasko, Douglas and Graff-Radford, Jonathan and Graff-Radford, Neill R and Hof, Patrick R and Krolak-Salmon, Pierre and Lehmann, Manja and Magnin, Eloi and Mendez, Mario F and Nestor, Peter J and Onyike, Chiadi U and Pelak, Victoria S and Pijnenburg, Yolande and Primativo, Silvia and Rossor, Martin N and Ryan, Natalie S and Scheltens, Philip and Shakespeare, Timothy J and Suárez González, Aida and Tang-Wai, David F and Yong, Keir X.X and Carrillo, Maria and Fox, Nick C and Alzheimer's Assoc ISTAART Atypical and Alzheimer's Association ISTAART Atypical Alzheimer's Disease and Associated Syndromes Professional Interest Area
Alzheimer's & Dementia: The Journal of the Alzheimer's Association, ISSN 1552-5260, 2017, Volume 13, Issue 8, pp. 870 - 884
Abstract Introduction A classification framework for posterior cortical atrophy (PCA) is proposed to improve the uniformity of definition of the syndrome in a... 
Neurology | Biomarker | Pathophysiology | Posterior cortical atrophy | Clinico-radiological syndrome | Alzheimer's disease | Clinical Neurology | Psychiatry and Mental health | Health Policy | Epidemiology | Cellular and Molecular Neuroscience | Developmental Neuroscience | Geriatrics and Gerontology | HEIDENHAIN VARIANT | COGNITIVE PROFILE | DEMENTIA | ALZHEIMERS ASSOCIATION WORKGROUPS | CLINICAL NEUROLOGY | NATIONAL INSTITUTE | GENETIC RISK | DIAGNOSTIC GUIDELINES | BALINTS SYNDROME | CREUTZFELDT-JAKOB-DISEASE | CORTICOBASAL DEGENERATION | Brain - diagnostic imaging | Brain Diseases - diagnostic imaging | Brain Diseases - classification | Humans | Brain Diseases - physiopathology | Brain Diseases - psychology | Alzheimer’s disease
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