Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Katalin, Majtényi"'
Autor:
Gabor G. Kovacs, Krisztina Danics, Katalin Majtényi, Susanne Schmid, Klára Törő, Irene Erber, Istvan Kapas, Shelley L. Forrest
Publikováno v:
Journal of Neural Transmission
Infectious agents, including viruses and bacteria, are proposed to be involved in the pathogenesis of Alzheimer’s disease (AD). According to this hypothesis, these agents have capacity to evade the host immune system leading to chronic infection, i
Autor:
Annemieke J.M. Rozemuller, Irina Alafuzoff, J. C. van Swieten, Herbert Budka, Andy King, Olaf Ansorge, Claire Troakes, Tatjana Nilsson, Hans A. Kretzschmar, Ellen Gelpi, Gabor G. Kovacs, James W. Ironside, Katalin Majtényi, Isidro Ferrer, Istvan Bodi, Nenad Bogdanovic, Giorgio Giaccone, Margaret M. Esiri, Thomas Arzberger, Irene Leisser, Tibor Hortobágyi, Safa Al-Sarraj
Publikováno v:
Neuropathology and Applied Neurobiology. 39:166-178
G. G. Kovacs, A. J. M. Rozemuller, J. C. van Swieten, E. Gelpi, K. Majtenyi, S. Al-Sarraj, C. Troakes, I. Bodi, A. King, T. Hortobagyi, M. M. Esiri, O. Ansorge, G. Giaccone, I. Ferrer, T. Arzberger, N. Bogdanovic, T. Nilsson, I. Leisser, I. Alafuzoff
Publikováno v:
Metabolic Brain Disease. 27:231-235
In the present study we evaluated cases referred as suspected Creutzfeldt-Jakob disease (CJD). Five out of 59 without prion disease showed neuropathological features of pellagra encephalopathy with widespread chromatolytic neurons (age range 40-48 ye
Autor:
Gabor G. Kovacs, Nathalie Streichenberger, Istvan Kapas, Raphael Sciot, Romana Höftberger, Anne Gaëlle Biacabe, jérémie Seguin, Lajos László, Isabelle Quadrio, Rik Vandenberghe, David Meyronet, Armand Perret-Liaudet, Katalin Majtényi, Thomas Ströbel, Herbert Budka
Publikováno v:
Acta Neuropathologica. 121:39-57
The E200K mutation is the most frequent prion protein gene (PRNP) mutation detected worldwide that is associated with Creutzfeldt-Jakob disease (CJD) and thought to have overlapping features with sporadic CJD, yet detailed neuropathological studies h
Autor:
Jill R. Murrell, Sandor Horvath, Bernardino Ghetti, Herbert Budka, Laszlo Haraszti, Mária Judit Molnár, Salvatore Spina, Gabor G. Kovacs, Katalin Majtényi
Publikováno v:
Movement Disorders. 24:1842-1847
TDP-43 has been identified as the pathological protein in the majority of cases of frontotemporal lobar degeneration and amyotrophic lateral sclerosis (ALS). TARDBP mutations have so far been uniquely associated with familial and sporadic ALS. We des
Autor:
Gabor G. Kovacs, Romana Höftberger, Jill R. Murrell, Michel Goedert, Herbert Budka, Salvatore Spina, R. Anthony Crowther, Bernardino Ghetti, Ellen Gelpi, Katalin Majtényi, Graham Fraser
Publikováno v:
Journal of Neuropathology & Experimental Neurology. 67:963-975
Frontotemporal lobar degenerations are a group of disorders characterized by circumscribed degeneration of the frontal and temporal lobes and diverse histopathological features. We report clinical, neuropathological, ultrastructural, biochemical and
Autor:
Katalin Majtényi, Gabor G. Kovacs, Eva Keller, Monika Cs. Horvath, Viktor Kovari, Yasmin L. Hurd
Publikováno v:
The Journal of Neuroscience. 27:13371-13375
Dysfunction of mesocorticolimbic dopaminergic neurons is considered a common feature of all drugs of abuse, yet few investigations have evaluated the dopamine (DA) system in nonstimulant human abusers. We examined mRNA expression levels of DA transpo
Autor:
Katalin Majtényi, Gabor G. Kovacs, Mirjam I. Lutz, Monika Cs. Horvath, Eva Keller, Yasmin L. Hurd
The observation of increased hyperphosphorylated tau levels correlating with microglial activation in opiate abusers has been interpreted as predisposition to accelerated Alzheimer diseaseerelated changes. The present study focused on evaluating addi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a985af71aa7f49a4e8dc18c87217ce51
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-267187
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-267187
Autor:
Eva Mitrova, Thomas Ströbel, Lajos László, Janos Minarovits, Agnes Bakos, Gabor G. Kovacs, Balázs Vajna, Matthew Bishop, Katalin Majtényi
Publikováno v:
Neurology. 65:1666-1669
The authors performed analysis of the prion protein gene (PRNP) in 27 out of 109 confirmed prion disease patients between 1994 and 2004. E200K mutation was found in 17 cases. Another 10 patients, lacking PRNP analysis, showed positive family history.
Autor:
Romana Höftberger, Sámuel Komoly, Gábor Jakab, Herbert Budka, Katalin Majtényi, Hans Lassmann, Gabor G. Kovacs, Péter Barsi, Rita Horváth
Publikováno v:
Brain. 128:35-41
Leber's hereditary optic neuropathy (LHON) is associated with point mutations in the mitochondrial DNA (mtDNA), coding for a mitochondrial respiratory chain complex I subunit. It is characterized by bilateral, usually sequential, optic neuropathy and