المؤلفون: Zhang M, Ferrari R, Tartaglia MC, Keith J, Surace EI, Wolf U, Sato C, Grinberg M, Liang Y, Xi Z, Dupont K, McGoldrick P, Weichert A, McKeever PM, Schneider R, McCorkindale MD, Manzoni C, Rademakers R, Graff-Radford NR, Dickson DW, Parisi JE, Boeve BF, Petersen RC, Miller BL, Seeley WW, van Swieten JC, van Rooij J, Pijnenburg Y, van der Zee J, Van Broeckhoven C, Le Ber I, Van Deerlin V, Suh E, Rohrer JD, Mead S, Graff C, Öijerstedt L, Pickering-Brown S, Rollinson S, Rossi G, Tagliavini F, Brooks WS, Dobson-Stone C, Halliday GM, Hodges JR, Piguet O, Binetti G, Benussi L, Ghidoni R, Nacmias B, Sorbi S, Bruni AC, Galimberti D, Scarpini E, Rainero I, Rubino E, Clarimon J, Lleó A, Ruiz A, Hernández I, Pastor P, Diez-Fairen M, Borroni B, Pasquier F, Deramecourt V, Lebouvier T, Perneczky R, Diehl-Schmid J, Grafman J, Huey ED, Mayeux R, Nalls MA, Hernandez D, Singleton A, Momeni P, Zeng Z, Hardy J, Robertson J, Zinman L, Rogaeva E, International FTD-Genomics Consortium (Ferrari R, Hernandez DG, Ramasamy A, Kwok JBJ, Schofield PR, Bartley L, Thompson E, Boada M, Padovani A, Cruchaga C, Cairns NJ, Forloni G, Albani D, Fenoglio C, Serpente M, Clarimón J, Blesa R, Wald Ouml ML, Nilsson K, Nilsson C, Mackenzie IRA, Hsiung GR, Mann DMA, Morris CM, Attems J, Griffiths TD, McKeith IG, Thomas AJ, Pietrini P, Wassermann EM, Baborie A, Jaros E, Tierney MC, Razquin C, Ortega-Cubero S, Alonso E, Alexopoulos P, Kurz A, Pinessi L, St George-Hyslop P, Giaccone G, Rowe JB, Schlachetzki JCM, Uphill J, Collinge J, Danek A, Van Deerlin VM, Grossman M, Trojanowski JQ, Cappa SF, Leber I, Hannequin D, Golfier V, Vercelletto M, Brice A, Bagnoli S, Piaceri I, Nielsen JE, Hjermind LE, Riemenschneider M, Mayhaus M, Ibach B, Gasparoni G, Pichler S, Gu W, Rossor MN, Fox NC, Warren JD, Grazia Spillantini M, Morris HR, Rizzu P, Heutink P, Snowden JS, Richardson A, Gerhard A, Maletta R, Frangipane F, Cupidi C, Bernardi L, Anfossi M, Gallo M, Elena Conidi M, Smirne N, Baker M, Knopman D, Josephs KA, Karydas AM, Rosen H, Dopper EGP, Seelaar H, Pijnenburg YAL, Scheltens P, Logroscino G, Capozzo R, Novelli V, Puca AA, Franceschi M, Postiglione A, Milan G, Sorrentino P, Kristiansen M, Chiang HH, Rollin A, Kapogiannis D, Ferrucci L, Singleton AB, Momeni P. )

المساهمون: Zhang M, Ferrari R, Tartaglia MC, Keith J, Surace EI, Wolf U, Sato C, Grinberg M, Liang Y, Xi Z, Dupont K, McGoldrick P, Weichert A, McKeever PM, Schneider R, McCorkindale MD, Manzoni C, Rademakers R, Graff-Radford NR, Dickson DW, Parisi JE, Boeve BF, Petersen RC, Miller BL, Seeley WW, van Swieten JC, van Rooij J, Pijnenburg Y, van der Zee J, Van Broeckhoven C, Le Ber I, Van Deerlin V, Suh E, Rohrer JD, Mead S, Graff C, Öijerstedt L, Pickering-Brown S, Rollinson S, Rossi G, Tagliavini F, Brooks WS, Dobson-Stone C, Halliday GM, Hodges JR, Piguet O, Binetti G, Benussi L, Ghidoni R, Nacmias B, Sorbi S, Bruni AC, Galimberti D, Scarpini E, Rainero I, Rubino E, Clarimon J, Lleó A, Ruiz A, Hernández I, Pastor P, Diez-Fairen M, Borroni B, Pasquier F, Deramecourt V, Lebouvier T, Perneczky R, Diehl-Schmid J, Grafman J, Huey ED, Mayeux R, Nalls MA, Hernandez D, Singleton A, Momeni P, Zeng Z, Hardy J, Robertson J, Zinman L, Rogaeva E, International FTD-Genomics Consortium (Ferrari R, Hernandez DG, Nalls MA, Rohrer JD, Ramasamy A, Kwok JBJ, Dobson-Stone C, Brooks WS, Schofield PR, Halliday GM, Hodges JR, Piguet O, Bartley L, Thompson E, Hernández I, Ruiz A, Boada M, Borroni B, Padovani A, Cruchaga C, Cairns NJ, Benussi L, Binetti G, Ghidoni R, Forloni G, Albani D, Galimberti D, Fenoglio C, Serpente M, Scarpini E, Clarimón J, Lleó A, Blesa R, Wald Ouml ML, Nilsson K, Nilsson C, Mackenzie IRA, Hsiung GR, Mann DMA, Grafman J, Morris CM, Attems J, Griffiths TD, McKeith IG, Thomas AJ, Pietrini P, Huey ED, Wassermann EM, Baborie A, Jaros E, Tierney MC, Pastor P, Razquin C, Ortega-Cubero S, Alonso E, Perneczky R, Diehl-Schmid J, Alexopoulos P, Kurz A, Rainero I, Rubino E, Pinessi L, Rogaeva E, St George-Hyslop P, Rossi G, Tagliavini F, Giaccone G, Rowe JB, Schlachetzki JCM, Uphill J, Collinge J, Mead S, Danek A, Van Deerlin VM, Grossman M, Trojanowski JQ, van der Zee J, Van Broeckhoven C, Cappa SF, Leber I, Hannequin D, Golfier V, Vercelletto M, Brice A, Nacmias B, Sorbi S, Bagnoli S, Piaceri I, Nielsen JE, Hjermind LE, Riemenschneider M, Mayhaus M, Ibach B, Gasparoni G, Pichler S, Gu W, Rossor MN, Fox NC, Warren JD, Grazia Spillantini M, Morris HR, Rizzu P, Heutink P, Snowden JS, Rollinson S, Richardson A, Gerhard A, Bruni AC, Maletta R, Frangipane F, Cupidi C, Bernardi L, Anfossi M, Gallo M, Elena Conidi M, Smirne N, Rademakers R, Baker M, Dickson DW, Graff-Radford NR, Petersen RC, Knopman D, Josephs KA, Boeve BF, Parisi JE, Seeley WW, Miller BL, Karydas AM, Rosen H, van Swieten JC, Dopper EGP, Seelaar H, Pijnenburg YAL, Scheltens P, Logroscino G, Capozzo R, Novelli V, Puca AA, Franceschi M, Postiglione A, Milan G, Sorrentino P, Kristiansen M, Chiang HH, Graff C, Pasquier F, Rollin A, Deramecourt V, Lebouvier T, Kapogiannis D, Ferrucci L, Pickering-Brown S, Singleton AB, Hardy J, Momeni P.)

Relation: info:eu-repo/semantics/altIdentifier/pmid/30252044; info:eu-repo/semantics/altIdentifier/wos/WOS:000446548400015; volume:141; issue:10; firstpage:2895; lastpage:2907; numberofpages:13; journal:BRAIN; http://hdl.handle.net/2318/1677461; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85054408708

الاتاحة: http://hdl.handle.net/2318/1677461
https://doi.org/10.1093/brain/awy238

المؤلفون: Rosso, Sonia, Kamphorst, W, de Graaf, Bianca, Willemsen, Rob, Ravid, R, Niermeijer, Martinus, Grazia Spillantini, M, Heutink, P, van Swieten, J.C.

المصدر: Rosso , S , Kamphorst , W , de Graaf , B , Willemsen , R , Ravid , R , Niermeijer , M , Grazia Spillantini , M , Heutink , P & van Swieten , J C 2001 , ' Familial frontotemporal dementia with ubiquitin-positive inclusions is linked to chromosome 17q21-22 ' , Brain , vol. 124 , pp. 1948-1957 . < http://hdl.handle.net/1765/9764 >

مصطلحات موضوعية: /dk/atira/pure/keywords/researchprograms/AFL001000/EMCMGC029601, name=EMC MGC-02-96-01, /dk/atira/pure/keywords/researchprograms/AFL001000/EMCMM044402, name=EMC MM-04-44-02

وصف الملف: application/pdf

الاتاحة: https://pure.eur.nl/en/publications/8aff5ba2-994d-4a5d-bfd1-4739c3f4cc85
https://pure.eur.nl/ws/files/46621741/11571213.pdf
http://hdl.handle.net/1765/9764

المؤلفون: Michel Goedert, R. Jakes, Grazia Spillantini M, Anthony Crowther R

مصطلحات موضوعية: Synucleinopathies, Parkinson's disease, business.industry, Dementia with Lewy bodies, Substantia nigra, medicine.disease, Nucleus basalis, medicine.anatomical_structure, Dorsal motor nucleus, nervous system, Cerebral cortex, medicine, Locus coeruleus, business, Neuroscience

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::dced3a1ef619256e80261c1eacca630d
https://doi.org/10.1385/1-59259-142-6:33

المؤلفون: Tolnay, M., Grazia Spillantini, M., Rizzini, C., Eccles, D., Lowe, J., Ellison, D.

المصدر: Neuropathology and Applied Neurobiology ; volume 26, issue 4, page 368-378 ; ISSN 0305-1846 1365-2990

الاتاحة: http://dx.doi.org/10.1046/j.1365-2990.2000.00109.x
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1046%2Fj.1365-2990.2000.00109.x
https://onlinelibrary.wiley.com/doi/pdf/10.1046/j.1365-2990.2000.00109.x