المؤلفون: Premi, Enrico, Grassi, Mario, van Swieten John, Galimberti, Daniela, Graff, Caroline, Masellis, Mario, Tartaglia, Carmela, Tagliavini, Fabrizio, Rowe James, B, Laforce, Robert, Finger, Elizabeth, Frisoni Giovanni, B, de Mendonça Alexandre, Sorbi, Sandro, Gazzina, Stefano, Cosseddu, Maura, Archetti, Silvana, Gasparotti, Roberto, Manes, Marta, Alberici, Antonella, Cardoso Manuel, J, Bocchetta, Martina, Cash David, M, Ourselin, Sebastian, Padovani, Alessandro, Rohrer Jonathan, D, Andersson, C, Arighi, A, Benussi, L, Binetti, G, Black, S, Dick, K, Fallström, M, Ferreira, C, Fenoglio, C, Fox, N, Freedman, M, Fumagalli, G, Ghidoni, R, Grisoli, M, Jelic, V, Jiskoot, L, Keren, R, Lombardi, G, Maruta, C, Meeter, L, Miltenberger-Miltényi, G, Nacmias, B, Öijerstedt, L, Panman, J, Pievani, M, Polito, C, Prioni, S, Rademakers, R, Redaelli, V, Rogaeva, E, Rossi, G, Rossor, M, Scarpini, E, Tang-Wai, D, Thomas, D, Thonberg, H, Tiraboschi, P, van Minkelen, R, Verdelho, A, Warren, J, Borroni, Barbara

المساهمون: Rowe, James [0000-0001-7216-8679], Apollo - University of Cambridge Repository, Neurology

المصدر: Brain, Vol. 140, No 6 (2017) pp. 1784-1791
Brain, 140, 1784-1791. Oxford University Press
Brain

مصطلحات موضوعية: Male, 0301 basic medicine, Oncology, frontotemporal dementia, Cognitive reserve, Frontotemporal dementia, Genetics, Structural MRI, TMEM106b, Cohort Studies, ddc:616.89, 0302 clinical medicine, C9orf72, genetics, Gray Matter, 10. No inequality, medicine.diagnostic_test, Middle Aged, cognitive reserve, Magnetic Resonance Imaging, medicine.anatomical_structure, structural MRI, Brain size, Educational Status, Female, Psychology, Adult, medicine.medical_specialty, Genotype, Prodromal Symptoms, Nerve Tissue Proteins, Grey matter, 03 medical and health sciences, Internal medicine, mental disorders, medicine, Humans, Dementia, Cerebral atrophy, Polymorphism, Genetic, Mini–Mental State Examination, Membrane Proteins, Original Articles, medicine.disease, Editor's Choice, 030104 developmental biology, Neurology (clinical), Atrophy, Neuroscience, 030217 neurology & neurosurgery

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2912bd538829bd1d0778669c836143f0
https://doi.org/10.1093/brain/awx103

المؤلفون: Mutsaerts, H. J. M. M., Mirza, S. S., Petr, J., Thomas, D. L., Cash, D. M., Bocchetta, M., De Vita, E., Metcalfe, A. W. S., Shirzadi, Z., Robertson, A. D., Tartaglia, M. C., Mitchell, S. B., Black, S. E., Freedman, M., Tang-Wai, D., Keren, R., Rogaeva, E., Van Swieten, J., Laforce, R., Tagliavini, F., Borroni, B., Galimberti, D., Rowe, J. B., Graff, C., Frisoni, G. B., Finger, E., Sorbi, S., De Mendonca, A., Rohrer, J. D., Macintosh, B. J., Masellis, M., Andersson, C., Archetti, S., Arighi, A., Benussi, L., Binetti, G., Cosseddu, M., Dick, K. M., Fallstrom, M., Ferreira, C., Fenoglio, C., Fox, N. C., Fumagalli, G., Gazzina, S., Ghidoni, R., Grisoli, M., Jelic, V., Jiskoot, L., Lombardi, G., Maruta, C., Mead, S., Meeter, L., Van Minkelen, R., Nacmias, B., Oijerstedt, L., Ourselin, S., Padovani, A., Panman, J., Pievani, M., Polito, C., Premi, E., Prioni, S., Rademakers, R., Redaelli, V., Rossi, G., Rossor, M. N., Scarpini, E., Thonberg, H., Tiraboschi, P., Verdelho, A., Warren, J. D.

المساهمون: Rowe, James [0000-0001-7216-8679], Apollo - University of Cambridge Repository, Neurology, Amsterdam Neuroscience - Neurodegeneration, Radiology and Nuclear Medicine

المصدر: Brain, 142, 1108-1120. Oxford University Press
Brain 142(2019), 1108-1120
Brain, 142(4), 1108-1120. Oxford University Press
Mutsaerts, H J M M, Mirza, S S, Petr, J, Thomas, D L, Cash, D M, Bocchetta, M, de Vita, E, Metcalfe, A W S, Shirzadi, Z, Robertson, A D, Tartaglia, M C, Mitchell, S B, Black, S E, Freedman, M, Tang-Wai, D, Keren, R, Rogaeva, E, van Swieten, J, Laforce, R, Tagliavini, F, Borroni, B, Galimberti, D, Rowe, J B, Graff, C, Frisoni, G B, Finger, E, Sorbi, S, de Mendonça, A, Rohrer, J D, MacIntosh, B J, Masellis, M & GENetic Frontotemporal dementia Initiative (GENFI) 2019, ' Cerebral perfusion changes in presymptomatic genetic frontotemporal dementia: a GENFI study ', Brain, vol. 142, no. 4, pp. 1108-1120 . https://doi.org/10.1093/brain/awz039
Brain
Brain, Vol. 142, No 4 (2019) pp. 1108-1120

مصطلحات موضوعية: 0301 basic medicine, Male, Pathology, Tau Proteins/genetics, cerebral blood flow, Gene mutation, Neuropsychological Tests, Arterial spin labelling, Frontotemporal Dementia/genetics, 0302 clinical medicine, Progranulins, C9orf72, Brain, Middle Aged, Corrigenda, Magnetic Resonance Imaging, Cerebral blood flow, Cerebrovascular Circulation, Frontotemporal Dementia, Female, arterial spin labelling, Frontotemporal dementia, Adult, medicine.medical_specialty, Heterozygote, genetic frontotemporal dementia, presymptomatic biomarker, C9orf72 Protein/genetics, tau Proteins, Progranulins/genetics, 03 medical and health sciences, Neuroimaging, mental disorders, medicine, Brain/metabolism, Dementia, Humans, Cerebral perfusion pressure, Aged, C9orf72 Protein, business.industry, Original Articles, Voxel-based morphometry, medicine.disease, arterial spin labeling, ddc:616.8, Genetic frontotemporal dementia, Presymptomatic biomarker, 030104 developmental biology, Cross-Sectional Studies, Mutation, Neurology (clinical), business, 030217 neurology & neurosurgery, Cerebrovascular Circulation/genetics

وصف الملف: application/vnd.openxmlformats-officedocument.wordprocessingml.document; application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09e0ddfbe25621d6c4cf2ffae1c139b3
https://www.repository.cam.ac.uk/handle/1810/290816