Kovacs GG - Search Results

1

I716F AβPP mutation associates with the deposition of oligomeric pyroglutamate amyloid-β and α-synucleinopathy with Lewy bodies.

Sieczkowski E, Milenkovic I, Venkataramani V, Giera R, Ströbel T, Höftberger R, Liberski PP, Auff E, Wirths O, Bayer TA, Kovacs GG. Sieczkowski E, et al. Among authors: kovacs gg. J Alzheimers Dis. 2015;44(1):103-14. doi: 10.3233/JAD-141524. J Alzheimers Dis. 2015. PMID: 25182745

2

Creutzfeldt-Jakob disease and inclusion body myositis: abundant disease-associated prion protein in muscle.

Kovacs GG, Lindeck-Pozza E, Chimelli L, Araújo AQ, Gabbai AA, Ströbel T, Glatzel M, Aguzzi A, Budka H. Kovacs GG, et al. Ann Neurol. 2004 Jan;55(1):121-5. doi: 10.1002/ana.10813. Ann Neurol. 2004. PMID: 14705121

3

Complement activation in human prion disease.

Kovacs GG, Gasque P, Ströbel T, Lindeck-Pozza E, Strohschneider M, Ironside JW, Budka H, Guentchev M. Kovacs GG, et al. Neurobiol Dis. 2004 Feb;15(1):21-8. doi: 10.1016/j.nbd.2003.09.010. Neurobiol Dis. 2004. PMID: 14751767

4

Natively unfolded tubulin polymerization promoting protein TPPP/p25 is a common marker of alpha-synucleinopathies.

Kovács GG, László L, Kovács J, Jensen PH, Lindersson E, Botond G, Molnár T, Perczel A, Hudecz F, Mezo G, Erdei A, Tirián L, Lehotzky A, Gelpi E, Budka H, Ovádi J. Kovács GG, et al. Among authors: kovacs j. Neurobiol Dis. 2004 Nov;17(2):155-62. doi: 10.1016/j.nbd.2004.06.006. Neurobiol Dis. 2004. PMID: 15474353

5

Neuropathology of white matter disease in Leber's hereditary optic neuropathy.

Kovács GG, Höftberger R, Majtényi K, Horváth R, Barsi P, Komoly S, Lassmann H, Budka H, Jakab G. Kovács GG, et al. Brain. 2005 Jan;128(Pt 1):35-41. doi: 10.1093/brain/awh310. Epub 2004 Oct 13. Brain. 2005. PMID: 15483043

6

Prion disease with a 144 base pair insertion: unusual cerebellar prion protein immunoreactivity.

Gelpi E, Kovacs GG, Ströbel T, Koperek O, Voigtländer T, Liberski PP, Budka H. Gelpi E, et al. Among authors: kovacs gg. Acta Neuropathol. 2005 Nov;110(5):513-9. doi: 10.1007/s00401-005-1073-x. Epub 2005 Sep 10. Acta Neuropathol. 2005. PMID: 16155763

7

Increased incidence of genetic human prion disease in Hungary.

Kovács GG, László L, Bakos A, Minárovits J, Bishop MT, Ströbel T, Vajna B, Mitrova E, Majtényi K. Kovács GG, et al. Neurology. 2005 Nov 22;65(10):1666-9. doi: 10.1212/01.wnl.0000184513.95290.80. Neurology. 2005. PMID: 16301504

8

The brain-specific protein TPPP/p25 in pathological protein deposits of neurodegenerative diseases.

Kovács GG, Gelpi E, Lehotzky A, Höftberger R, Erdei A, Budka H, Ovádi J. Kovács GG, et al. Acta Neuropathol. 2007 Feb;113(2):153-61. doi: 10.1007/s00401-006-0167-4. Epub 2006 Nov 23. Acta Neuropathol. 2007. PMID: 17123092

9

Involvement of the endosomal-lysosomal system correlates with regional pathology in Creutzfeldt-Jakob disease.

Kovács GG, Gelpi E, Ströbel T, Ricken G, Nyengaard JR, Bernheimer H, Budka H. Kovács GG, et al. J Neuropathol Exp Neurol. 2007 Jul;66(7):628-36. doi: 10.1097/nen.0b013e318093ecc7. J Neuropathol Exp Neurol. 2007. PMID: 17620988

10

MAPT S305I mutation: implications for argyrophilic grain disease.

Kovacs GG, Pittman A, Revesz T, Luk C, Lees A, Kiss E, Tariska P, Laszlo L, Molnár K, Molnar MJ, Tolnay M, de Silva R. Kovacs GG, et al. Acta Neuropathol. 2008 Jul;116(1):103-18. doi: 10.1007/s00401-007-0322-6. Epub 2007 Dec 8. Acta Neuropathol. 2008. PMID: 18066559

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