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Lancet neurology, ISSN 1474-4422, 2015, Volume 14, Issue 10, pp. 1002 - 1009
Journal Article
by Majounie, Elisa, PhD and Renton, Alan E, PhD and Mok, Kin, MSc and Dopper, Elise GP and Waite, Adrian, PhD and Rollinson, Sara, PhD and Chiò, Adriano, MD and Restagno, Gabriella, MD and Nicolaou, Nayia, MSc and Simon-Sanchez, Javier, PhD and van Swieten, John C, Prof and Abramzon, Yevgeniya and Johnson, Janel O, PhD and Sendtner, Michael, Prof and Pamphlett, Roger, MD and Orrell, Richard W, MD and Mead, Simon, MD and Sidle, Katie C, MD and Houlden, Henry, Prof and Rohrer, Jonathan D, MD and Morrison, Karen E, Prof and Pall, Hardev, MD and Talbot, Kevin, Prof and Ansorge, Olaf, MD and Hernandez, Dena G, MSc and Arepalli, Sampath, MS and Sabatelli, Mario, MD and Mora, Gabriele, MD and Corbo, Massimo, MD and Giannini, Fabio, MD and Calvo, Andrea, MD and Englund, Elisabet, MD and Borghero, Giuseppe, MD and Floris, Gian Luca, MD and Remes, Anne M, Prof and Laaksovirta, Hannu, MD and McCluskey, Leo, MD and Trojanowski, John Q, Prof and Van Deerlin, Vivianna M, MD and Schellenberg, Gerard D, Prof and Nalls, Michael A, PhD and Drory, Vivian E, MD and Lu, Chin-Song, Prof and Yeh, Tu-Hsueh, MD and Ishiura, Hiroyuki, MD and Takahashi, Yuji, MD and Tsuji, Shoji, Prof and Le Ber, Isabelle, MD and Brice, Alexis, Prof and Drepper, Carsten, PhD and Williams, Nigel, PhD and Kirby, Janine, PhD and Shaw, Pamela, Prof and Hardy, John, Prof and Tienari, Pentti J, MD and Heutink, Peter, Prof and Morris, Huw R, MD and Pickering-Brown, Stuart, Prof and Traynor, Bryan J, Dr and The Chromosome 9-ALS/FTD Consortium and The ITALSGEN Consortium and The French research network on FTLD/FTLD/ALS and Chromosome 9-ALS FTD Consortium and French Res Network FTLD FTLD ALS and ITALSGEN Consortium and French research network on FTLD/FTLD/ALS and Chromosome 9-ALS/FTD Consortium
Lancet neurology, ISSN 1474-4422, 2012, Volume 11, Issue 4, pp. 323 - 330
Neurology | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Frontotemporal Dementia - genetics | Cross-Sectional Studies | DNA Repeat Expansion - genetics | Amyotrophic Lateral Sclerosis - genetics | Humans | Middle Aged | Child, Preschool | Genotype | Male | Genetic Loci | Open Reading Frames - genetics | Young Adult | Chromosomes, Human, Pair 9 - genetics | Adolescent | Age of Onset | Aged, 80 and over | Adult | Female | Aged | Child | Cohort Studies | Medical research | Medical colleges | Care and treatment | Nervous system diseases | Neurosciences | Molecular genetics | Oncology, Experimental | Questions and answers | Amyotrophic lateral sclerosis | Research | Medicine, Experimental | Agriculture | Physicians (General practice) | Alzheimer's disease | Dementia | Cancer | Biomedical engineering | Index Medicus | Haplotypes | Polymerase chain reaction | Neurodegenerative diseases | Ethnic groups | Data processing | Mutation | Frontotemporal dementia | Genetic counselling | Islands | Age | Toll-Like Receptor 4 | Open Reading Frames | Adaptor Proteins, Vesicular Transport | Lipopolysaccharides | Life Sciences | DNA Repeat Expansion | Interferon Regulatory Factor-3 | Transfection | Amyotrophic Lateral Sclerosis | RNA Interference | HEK293 Cells | Membrane Glycoproteins | Vesicular Transport Proteins | Protein Structure, Tertiary | Cell Line | Chemokine CCL5 | Frontotemporal Dementia | Signal Transduction | Myeloid Differentiation Factor 88 | Chromosomes, Human, Pair 9 | Protein Transport | Adaptor Proteins, Signal Transducing | Santé publique et épidémiologie | RNA, Small Interfering | Endosomes | Neurologi | Clinical Medicine | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap
Journal Article
Stroke (1970), ISSN 0039-2499, 04/2012, Volume 43, Issue 4, pp. 980 - 986
Journal Article
The journals of gerontology. Series A, Biological sciences and medical sciences, ISSN 1079-5006, 05/2010, Volume 65 A, Issue 5, pp. 478 - 487
Journal Article
PloS one, ISSN 1932-6203, 05/2017, Volume 12, Issue 5, pp. e0175674 - e0175674
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Brain-Derived Neurotrophic Factor - genetics | Dopamine Plasma Membrane Transport Proteins - metabolism | Parkinson Disease - complications | Humans | Middle Aged | Tomography, Emission-Computed, Single-Photon | Male | tau Proteins - cerebrospinal fluid | Cognitive Dysfunction - cerebrospinal fluid | Catechol O-Methyltransferase - genetics | Diffusion Tensor Imaging | Magnetic Resonance Imaging | Cognitive Dysfunction - epidemiology | Aged, 80 and over | Amyloid beta-Peptides - cerebrospinal fluid | Adult | Cognitive Dysfunction - genetics | Female | Aged | Polymorphism, Single Nucleotide | Biomarkers - cerebrospinal fluid | Cognitive Dysfunction - diagnostic imaging | Complications and side effects | Care and treatment | Parkinson's disease | Development and progression | Cognition disorders | Biological markers | Identification and classification | Brain | Visual cortex | Cognitive ability | Nervous system | Cerebrospinal fluid | Risk factors | Eye | Design | Computed tomography | Education | Aging | Alzheimer's disease | Public health | Movement disorders | Deoxyribonucleic acid--DNA | Apolipoprotein E4 | Emotional behavior | Temporal lobe | Neurodegenerative diseases | Magnetic resonance | Catechol | Single photon emission computed tomography | Substrates | Neurology | Pathology | Thinning | Experimental design | Anisotropy | Biomarkers | β-Amyloid | Dementia | Neuroimaging | Haplotypes | Mental disorders | Laboratories | Parkinsons disease | Visual perception | Atrophy | Dementia disorders | Dopamine | Review boards | Health risks | Pharmacology | Dentistry | Medicine | Brain research | Sleep | Brain-derived neurotrophic factor | Magnetic resonance imaging | Parietal lobe | Alzheimers disease | Psychiatry | Polymorphism | Index Medicus | Medicin och hälsovetenskap | Deoxyribonucleic acid | DNA
Journal Article