Sortiert nach Autor

Publikationen - sortiert nach Autor

• Klotz S, König T, Erdler M, Ulram A, Nguyen A, Ströbel T, Zimprich A, Stögmann E, Regelsberger G, Höftberger R, Budka H, Kovacs G, Gelpi E (2020) Co‐incidental C9orf72 expansion mutation‐related frontotemporal lobar degeneration pathology and sporadic Creutzfeldt−Jakob disease Eur J Neurol,

• Cetin H, Wöhrer A, Rittelmeyer I, Gencik M, Zulehner G, Zimprich F, Ströbel T, Zimprich A (2016) The c.65-2A>G splice site mutation is associated with a mild phenotype in Danon disease due to the transcription of normal LAMP2 mRNA Clin Genet, 90 (4): 366-371
• Kovacs G, Rahimi J, Ströbel T, Lutz M, Regelsberger G, Streichenberger N, Perret-Liaudet A, Höftberger R, Liberski P, Budka H, Sikorska B (2016) Tau Pathology in Creutzfeldt-Jakob Disease Revisited Brain Pathol,
• Alexander J, Kalev O, Mehrabian S, Traykov L, Raycheva M, Kanakis D, Drineas P, Lutz M, Ströbel T, Penz T, Schuster M, Bock C, Ferrer I, Paschou P, Kovacs G (2016) Familial early-onset dementia with complex neuropathologic phenotype and genomic background Neurobiol Aging, 42: 199-204
• Kovacs G, Lutz M, Ricken G, Ströbel T, Höftberger R, Preusser M, Regelsberger G, Hönigschnabl S, Reiner A, Fischer P, Budka H, Hainfellner J (2016) Dura mater is a potential source of Aβ seeds Acta Neuropathol, 131 (6): 911-923

• Sieczkowski E, Milenkovic I, Venkataramani V, Giera R, Ströbel T, Höftberger R, Liberski PP, Auff E, Wirths O, Bayer TA, Kovacs GG. (2015) I716F AβPP mutation associates with the deposition of oligomeric pyroglutamate amyloid-β and α-synucleinopathy with Lewy bodies. J Alzheimers Dis, 44: 103-114
• Berghoff A, Trummert A, Unterberger U, Ströbel T, Hortobágyi T, Kovacs GG (2015) Atypical sporadic CJD-MM phenotype with white matter kuru plaques associated with intranuclear inclusion body and argyrophilic grain disease Neuropathology, 35 (4): 336-342
• Sanchez-Juan P, Bishop M, Kovacs G, Calero M, Aulchenko Y, Ladogana A, Boyd A, Lewis V, Ponto C, Calero O, Poleggi A, Carracedo �, van der Lee S, Ströbel T, Rivadeneira F, Hofman A, Haïk S, Combarros O, Berciano J, Uitterlinden A, Collins S, Budka H, Brandel J, Laplanche J, Pocchiari M, Zerr I, Knight R, Will R, van Duijn C (2015) A Genome Wide Association Study Links Glutamate Receptor Pathway to Sporadic Creutzfeldt-Jakob Disease Risk PlosOne, 10 (4): e0123654
• Kovacs GG, van der Zee J, Hort J, Kristoferitsch W, Leitha T, Höftberger R, Ströbel T, Van Broeckhoven C, Matej R (2015) Clinicopathological description of two cases withSQSTM1gene mutation associated with frontotemporal dementia Neuropathology, 36 (1): 27-38

• van der Zee J, Gijselinck I, Dillen L, Van Langenhove T, Theuns J, Engelborghs S, Philtjens S, Vandenbulcke M, Sleegers K, Sieben A, Bäumer V, Maes G, Corsmit E, Borroni B, Padovani A, Archetti S, Perneczky R, Diehl-Schmid J, de Mendonça A, Miltenberger-Miltenyi G, Pereira S, Pimentel J, Nacmias B, Bagnoli S, Sorbi S, Graff C, Chiang H, Westerlund M, Sanchez-Valle R, Llado A, Gelpi E, Santana I, Almeida M, Santiago B, Frisoni G, Zanetti O, Bonvicini C, Synofzik M, Maetzler W, vom Hagen J, Schöls L, Heneka M, Jessen F, Matej R, Parobkova E, Kovacs G, Ströbel T, Sarafov S, Tournev I, Jordanova A, Danek A, Arzberger T, Fabrizi G, Testi S, Salmon E, Santens P, Martin J, Cras P, Vandenberghe R, De Deyn P, Cruts M, Van Broeckhoven C, van der Zee J, Gijselinck I, Dillen L, Van Langenhove T, Theun (2013) A Pan-European Study of the C9orf72 Repeat Associated with FTLD: Geographic Prevalence, Genomic Instability, and Intermediate Repeats Hum Mut, 34 (2): 363-373
• Ehling R, Nosková L, Stránecký V, Hartmannová H, Přistoupilová A, Hodaňová K, Benke T, Kovacs G, Ströbel T, Niedermüller U, Wagner M, Nachbauer W, Janecke A, Budka H, Boesch S, Kmoch S (2013) Cerebellar dysfunction in a family harboring the PSEN1 mutation co-segregating with a Cathepsin D variant p.A58V J Neurol Sci, 326 (1-2): 75-82
• Kovacs G, Peden A, Weis S, Höftberger R, Berghoff A, Yull H, Ströbel T, Koppi S, Katzenschlager R, Langenscheidt D, Assar H, Zaruba E, Gröner A, Voigtländer T, Puska G, Hametner E, Grams A, Muigg A, Knoflach M, László L, Ironside J, Head M, Budka H (2013) Rapidly progressive dementia with thalamic degeneration and peculiar cortical prion protein immunoreactivity, but absence of proteinase K resistant PrP: a new disease entity? Acta Neuropathologica Communications, 1 (1): 72