المؤلفون: Schols, L, Rattay, TW, Martus, P, Meisner, C, Baets, J, Fischer, I, Jagle, C, Fraidakis, MJ, Martinuzzi, A, Saute, JA, Scarlato, M, Antenora, A, Stendel, C, Hoflinger, P, Lourenco, CM, Abreu, L, Smets, K, Paucar, M, Deconinck, T, Bis, DM, Wiethoff, S, Bauer, P, Arnoldi, A, Marques, W, Jardim, LB, Hauser, S, Criscuolo, C, Filla, A, Zuchner, S, Bassi, MT, Klopstock, T, De Jonghe, P, Bjorkhem, I, Schule, R

المصدر: Brain : a journal of neurology. 140(12):3112-3127

مصطلحات موضوعية: Medicin och hälsovetenskap

URL الوصول: http://kipublications.ki.se/Default.aspx?queryparsed=id:137155329

المؤلفون: Theofilopoulos, S, Griffiths, WJ, Crick, PJ, Yang, SZ, Meljon, A, Ogundare, M, Kitambi, SS, Lockhart, A, Tuschl, K, Clayton, PT, Morris, AA, Martinez, A, Reddy, MA, Martinuzzi, A, Bassi, MT, Honda, A, Mizuochi, T, Kimura, A, Nittono, H, De Michele, G, Carbone, R, Criscuolo, C, Yau, JL, Seckl, JR, Schule, R, Schols, L, Sailer, AW, Kuhle, J, Fraidakis, MJ, Gustafsson, JA, Steffensen, KR, Bjorkhem, I, Ernfors, P, Sjovall, J, Arenas, E, Wang, YQ

المصدر: The Journal of clinical investigation. 124(11):4829-4842

مصطلحات موضوعية: Medicin och hälsovetenskap

URL الوصول: http://kipublications.ki.se/Default.aspx?queryparsed=id:130043022

المؤلفون: Fraidakis, MJ

المصدر: Journal of the history of the neurosciences. 19(3):239-252

مصطلحات موضوعية: Medicin och hälsovetenskap

URL الوصول: http://kipublications.ki.se/Default.aspx?queryparsed=id:120991348

المؤلفون: Fraidakis, MJ, Kiyotani, T, Pernold, K, Bergstrom, J, Olson, L

المصدر: Neuroreport. 18(2):185-189

مصطلحات موضوعية: Medicin och hälsovetenskap

URL الوصول: http://kipublications.ki.se/Default.aspx?queryparsed=id:12540103

المؤلفون: Fraidakis, MJ, Spenger, C, Olson, L

المصدر: Experimental neurology. 188(1):33-42

مصطلحات موضوعية: Medicin och hälsovetenskap

URL الوصول: http://kipublications.ki.se/Default.aspx?queryparsed=id:1927263

المؤلفون: Van der Zee, J, Gijselinck, I, Van Mossevelde, S, Perrone, F, Dillen, L, Heeman, B, Baumer, V, Engelborghs, S, De Bleecker, J, Baets, J, Gelpi, E, Rojas-Garcia, R, Clarimon, J, Lleo, A, Diehl-Schmid, J, Alexopoulos, P, Perneczky, R, Synofzik, M, Just, J, Schoels, L, Graff, C, Thonberg, H, Borroni, B, Padovani, A, Jordanova, A, Sarafov, S, Tournev, I, De Mendonca, A, Miltenberger-Miltenyi, G, Simoes do Couto, F, Ramirez, A, Jessen, F, Heneka, MT, Gomez-Tortosa, E, Danek, A, Cras, P, Vandenberghe, R, De Jonghe, P, De Deyn, PP, Sleegers, K, Cruts, M, Van Broeckhoven, C, Goeman, J, Nuytten, D, Smets, K, Robberecht, W, Van Damme, P, Santens, P, Dermaut, B, Versijpt, J, Michotte, A, Ivanoiu, A, Deryck, O, Bergmans, B, Delbeck, B, Bruyland, M, Willems, C, Salmon, E, Pastor, P, Ortega-Cubero, S, Benussi, L, Ghidoni, R, Binetti, G, Hernandez, I, Boada, M, Ruiz, A, Sorbi, S, Nacmias, B, Bagnoli, S, Sanchez-Valle, R, Llado, A, Santana, I, Almeida, MR, Frisoni, GB, Maetzler, W, Matej, R, Fraidakis, MJ, Kovacs, GG, Fabrizi, GM, Testi, S

المصدر: 309 ; 297

مصطلحات موضوعية: Science & Technology, Life Sciences & Biomedicine, Genetics & Heredity, TANK-Binding Kinase 1, TBK1, frontotemporal dementia, FTD, amyotrophic lateral sclerosis, ALS, mutations, NFkB luciferase reporter assay, LOBAR DEGENERATION, REPEAT EXPANSION, HEXANUCLEOTIDE REPEAT, ARGYROPHILIC GRAINS, DIAGNOSTIC-CRITERIA, BELGIAN COHORT, FAMILIAL ALS, C9ORF72, DISEASE, TDP-43, NFκB luciferase reporter assay

Relation: Human Mutation; http://hdl.handle.net/10044/1/45933; https://dx.doi.org/10.1002/humu.23161

الاتاحة: http://hdl.handle.net/10044/1/45933
https://doi.org/10.1002/humu.23161

المؤلفون: van der Zee J, Gijselinck I, Van Mossevelde S, Perrone F, Dillen L, Heeman B, Bäumer V, Engelborghs S, De Bleecker J, Baets J, Gelpi E, Rojas García R, Clarimón J, Lleó A, Diehl Schmid J, Alexopoulos P, Perneczky R, Synofzik M, Just J, Schöls L, Graff C, Thonberg H, Jordanova A, Sarafov S, Tournev I, de Mendonça A, Miltenberger Miltényi G, Simões do Couto F, Ramirez A, Jessen F, Heneka MT, Gómez Tortosa E, Danek A, Cras P, Vandenberghe R, De Jonghe P, De Deyn PP, Sleegers K, Cruts M, Van Broeckhoven C, Goeman J, Nuytten D, Smets K, Robberecht W, Damme PV, Bleecker J, Santens P, Dermaut B, Versijpt J, Michotte A, Ivanoiu A, Deryck O, Bergmans B, Delbeck J, Bruyland M, Willems C, Salmon E, Pastor P, Ortega Cubero S, Benussi L, Ghidoni R, Binetti G, Hernández I, Boada M, Ruiz A, Sorbi S, Nacmias B, Bagnoli S, Sanchez Valle R, Llado A, Santana I, Rosário Almeida M, Frisoni GB, Maetzler W, Matej R, Fraidakis MJ, Kovacs GG, Fabrizi GM, Testi S., BORRONI, Barbara, PADOVANI, Alessandro

المساهمون: van der Zee J, Gijselinck I, Van Mossevelde S, Perrone F, Dillen L, Heeman B, Bäumer V, Engelborghs S, De Bleecker J, Baets J, Gelpi E, Rojas García R, Clarimón J, Lleó, A, Diehl Schmid J, Alexopoulos P, Perneczky R, Synofzik M, Just J, Schöls L, Graff C, Thonberg H, Borroni Barbara, Padovani Alessandro, Jordanova A, Sarafov S, Tournev I, de Mendonça A, Miltenberger Miltényi G, Simões do Couto F, Ramirez A, Jessen F, Heneka Mt, Gómez Tortosa E, Danek A, Cras P, Vandenberghe R, De Jonghe P, De Deyn Pp, Sleegers K, Cruts M, Van Broeckhoven C, Goeman J, Nuytten D, Smets K, Robberecht W, Damme Pv, Bleecker J, Santens P, Dermaut B, Versijpt J, Michotte A, Ivanoiu A, Deryck O, Bergmans B, Delbeck J, Bruyland M, Willems C, Salmon E, Pastor P, Ortega Cubero S, Benussi L, Ghidoni R, Binetti G, Hernández I, Boada M, Ruiz A, Sorbi S, Nacmias B, Bagnoli S, Sanchez Valle R, Llado A, Santana I, Rosário Almeida M, Frisoni Gb, Maetzler W, Matej R, Fraidakis Mj, Kovacs Gg, Fabrizi Gm, Testi S.

Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000394905800010; journal:HUMAN MUTATION; http://hdl.handle.net/11379/492438; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85010775170

الاتاحة: http://hdl.handle.net/11379/492438

المؤلفون: Fraidakis MJ, Brunetti M, Blackstone C, Chiò A., FILIPPI , MASSIMO

المساهمون: Fraidakis, Mj, Brunetti, M, Blackstone, C, Filippi, Massimo, Chiò, A.

Relation: info:eu-repo/semantics/altIdentifier/pmid/27318863; info:eu-repo/semantics/altIdentifier/wos/WOS:000383215200011; volume:16; firstpage:373; lastpage:381; numberofpages:9; journal:NEURODEGENERATIVE DISEASES; http://hdl.handle.net/20.500.11768/18088

الاتاحة: https://hdl.handle.net/20.500.11768/18088
https://doi.org/10.1159/000444715

المؤلفون: Fraidakis, M. J., Brunetti, M., Blackstone, C., Filippi, M., Chio, A.

المساهمون: Fraidakis, Mj, Brunetti, M, Blackstone, C, Filippi, Massimo, Chiò, A.

مصطلحات موضوعية: Adult, Heterozygote, Magnetic Resonance Spectroscopy, Greece, Spastic Paraplegia, Hereditary, Spatacsin, European Continental Ancestry Group, Brain, Proteins, Magnetic Resonance Imaging, White People, Corpus Callosum, Pedigree, Diffusion tensor imaging, Hereditary spastic paraparesis, Leukoencephalopathy, Neurogenetics, Dementia, Diffusion Tensor Imaging, Female, Humans, Mutation, Hereditary, Spastic Paraplegia

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::4a9cc5c05dd56a2106cf393fc8615a1d