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István Katona
István Katona
Institute of Neuropathology, RWHT Aachen University
Bestätigte E-Mail-Adresse bei ukaachen.de
Titel
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Zitiert von
Jahr
Regulation of endoplasmic reticulum turnover by selective autophagy
A Khaminets, T Heinrich, M Mari, P Grumati, AK Huebner, M Akutsu, ...
Nature 522 (7556), 354-358, 2015
8192015
Transcriptional regulator PRDM12 is essential for human pain perception
YC Chen, M Auer-Grumbach, S Matsukawa, M Zitzelsberger, ...
Nature genetics 47 (7), 803-808, 2015
1752015
Transcriptional regulator PRDM12 is essential for human pain perception
YC Chen, M Auer-Grumbach, S Matsukawa, M Zitzelsberger, ...
Nature genetics 47 (7), 803-808, 2015
1752015
Altered localization, abnormal modification and loss of function of Sigma receptor-1 in amyotrophic lateral sclerosis
J Prause, A Goswami, I Katona, A Roos, M Schnizler, E Bushuven, ...
Human molecular genetics 22 (8), 1581-1600, 2013
1632013
Small-fiber neuropathy in patients with ALS
J Weis, I Katona, G Müller-Newen, C Sommer, G Necula, C Hendrich, ...
Neurology 76 (23), 2024-2029, 2011
1482011
Curcumin derivatives promote Schwann cell differentiation and improve neuropathy in R98C CMT1B mice
A Patzko, Y Bai, MA Saporta, I Katona, XY Wu, D Vizzuso, ML Feltri, ...
Brain 135 (12), 3551-3566, 2012
1222012
Shortened internodal length of dermal myelinated nerve fibres in Charcot–Marie-Tooth disease type 1A
MA Saporta, I Katona, RA Lewis, S Masse, ME Shy, J Li
Brain 132 (12), 3263-3273, 2009
1162009
Loss of function of the ALS protein SigR1 leads to ER pathology associated with defective autophagy and lipid raft disturbances
JT Vollrath, A Sechi, A Dreser, I Katona, D Wiemuth, J Vervoorts, ...
Cell death & disease 5 (6), e1290-e1290, 2014
1012014
Targeting myelin lipid metabolism as a potential therapeutic strategy in a model of CMT1A neuropathy
R Fledrich, T Abdelaal, L Rasch, V Bansal, V Schütza, B Brügger, ...
Nature communications 9 (1), 3025, 2018
1002018
PMP22 expression in dermal nerve myelin from patients with CMT1A
I Katona, X Wu, SME Feely, S Sottile, CE Siskind, LJ Miller, ME Shy, J Li
Brain 132 (7), 1734-1740, 2009
922009
The ALS-linked E102Q mutation in Sigma receptor-1 leads to ER stress-mediated defects in protein homeostasis and dysregulation of RNA-binding proteins
A Dreser, JT Vollrath, A Sechi, S Johann, A Roos, A Yamoah, I Katona, ...
Cell Death & Differentiation 24 (10), 1655-1671, 2017
902017
Cold-aggravated pain in humans caused by a hyperactive NaV1.9 channel mutant
E Leipold, A Hanson-Kahn, M Frick, P Gong, JA Bernstein, M Voigt, ...
Nature communications 6 (1), 10049, 2015
822015
Frequent genes in rare diseases: panel‐based next generation sequencing to disclose causal mutations in hereditary neuropathies
MF Dohrn, N Glöckle, L Mulahasanovic, C Heller, J Mohr, C Bauer, ...
Journal of neurochemistry 143 (5), 507-522, 2017
762017
Towards a functional pathology of hereditary neuropathies
J Weis, KG Claeys, A Roos, H Azzedine, I Katona, JM Schröder, ...
Acta neuropathologica 133, 493-515, 2017
742017
Conduction block in PMP22 deficiency
Y Bai, X Zhang, I Katona, MA Saporta, ME Shy, HA O'Malley, LL Isom, ...
Journal of Neuroscience 30 (2), 600-608, 2010
702010
A knock-in/knock-out mouse model of HSPB8-associated distal hereditary motor neuropathy and myopathy reveals toxic gain-of-function of mutant Hspb8
D Bouhy, M Juneja, I Katona, A Holmgren, B Asselbergh, V De Winter, ...
Acta neuropathologica 135, 131-148, 2018
672018
Diseases of the peripheral nerves
I Katona, J Weis
Handbook of clinical Neurology 145, 453-474, 2018
652018
Small‐fiber neuropathy with cardiac denervation in postural tachycardia syndrome
CA Haensch, M Tosch, I Katona, J Weis, S Isenmann
Muscle & nerve 50 (6), 956-961, 2014
592014
New findings in a global approach to dissect the whole phenotype of PLA2G6 gene mutations
MA Salih, E Mundwiller, AO Khan, A AlDrees, SA Elmalik, HH Hassan, ...
PLoS One 8 (10), e76831, 2013
542013
Macrophage depletion ameliorates peripheral neuropathy in aging mice
X Yuan, D Klein, S Kerscher, BL West, J Weis, I Katona, R Martini
Journal of Neuroscience 38 (19), 4610-4620, 2018
492018
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