متابعة
Michael Orth
Michael Orth
بريد إلكتروني تم التحقق منه على uni-ulm.de
عنوان
عدد مرات الاقتباسات
عدد مرات الاقتباسات
السنة
CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion
JM Lee, EM Ramos, JH Lee, T Gillis, JS Mysore, MR Hayden, SC Warby, ...
Neurology 78 (10), 690-695, 2012
4142012
Identification of genetic factors that modify clinical onset of Huntington’s disease
JM Lee, VC Wheeler, MJ Chao, JPG Vonsattel, RM Pinto, D Lucente, ...
Cell 162 (3), 516-526, 2015
4012015
Mitochondria and degenerative disorders
M Orth, AHV Schapira
American journal of medical genetics 106 (1), 27-36, 2001
3572001
The cortical silent period: intrinsic variability and relation to the waveform of the transcranial magnetic stimulation pulse
M Orth, JC Rothwell
Clinical neurophysiology 115 (5), 1076-1082, 2004
3202004
Neuropsychiatric symptoms in a European Huntington's disease cohort (REGISTRY)
E van Duijn, D Craufurd, AAM Hubers, EJ Giltay, R Bonelli, H Rickards, ...
Journal of Neurology, Neurosurgery & Psychiatry 85 (12), 1411-1418, 2014
2962014
Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study
DJH Moss, AF Pardiñas, D Langbehn, K Lo, BR Leavitt, R Roos, A Durr, ...
The Lancet Neurology 16 (9), 701-711, 2017
2832017
Observing Huntington's disease: the European Huntington's disease network's REGISTRY
M Orth, European Huntington's Disease Network
Journal of Neurology, Neurosurgery & Psychiatry 82 (12), 1409-1412, 2011
2672011
CAG repeat not polyglutamine length determines timing of Huntington’s disease onset
JM Lee, K Correia, J Loupe, KH Kim, D Barker, EP Hong, MJ Chao, ...
Cell 178 (4), 887-900. e14, 2019
2612019
Expression of mutant α-synuclein causes increased susceptibility to dopamine toxicity
SJ Tabrizi, M Orth, JM Wilkinson, JW Taanman, TT Warner, JM Cooper, ...
Human molecular genetics 9 (18), 2683-2689, 2000
2532000
Mitochondrial involvement in Parkinson’s disease
M Orth, AHV Schapira
Neurochemistry international 40 (6), 533-541, 2002
2462002
The variability of intracortical inhibition and facilitation
M Orth, AH Snijders, JC Rothwell
Clinical neurophysiology 114 (12), 2362-2369, 2003
2392003
Motor inhibition in patients with Gilles de la Tourette syndrome: functional activation patterns as revealed by EEG coherence
DJ Serrien, M Orth, AH Evans, AJ Lees, P Brown
Brain 128 (1), 116-125, 2005
2192005
The Gilles de la Tourette syndrome–Quality of Life Scale (GTS-QOL) development and validation
AE Cavanna, A Schrag, D Morley, M Orth, MM Robertson, E Joyce, ...
Neurology 71 (18), 1410-1416, 2008
2142008
Multispectral brain morphometry in Tourette syndrome persisting into adulthood
B Draganski, D Martino, AE Cavanna, C Hutton, M Orth, MM Robertson, ...
Brain 133 (12), 3661-3675, 2010
1662010
Structural changes in the somatosensory system correlate with tic severity in Gilles de la Tourette syndrome
G Thomalla, HR Siebner, M Jonas, T Bäumer, K Biermann-Ruben, ...
Brain 132 (3), 765-777, 2009
1652009
An exploratory double‐blind, randomized clinical trial with selisistat, a SirT1 inhibitor, in patients with H untington's disease
SD Süssmuth, S Haider, GB Landwehrmeyer, R Farmer, C Frost, ...
British journal of clinical pharmacology 79 (3), 465-476, 2015
1602015
Primary focal dystonia: evidence for distinct neuropsychiatric and personality profiles
R Lencer, S Steinlechner, J Stahlberg, H Rehling, M Orth, T Baeumer, ...
Journal of Neurology, Neurosurgery & Psychiatry 80 (10), 1176-1179, 2009
1522009
Consensus paper on short-interval intracortical inhibition and other transcranial magnetic stimulation intracortical paradigms in movement disorders
A Berardelli, G Abbruzzese, R Chen, M Orth, MC Ridding, C Stinear, ...
Brain stimulation 1 (3), 183-191, 2008
1522008
Excitability of motor cortex inhibitory circuits in Tourette syndrome before and after single dose nicotine
M Orth, B Amann, MM Robertson, JC Rothwell
Brain 128 (6), 1292-1300, 2005
1482005
The HTT CAG-expansion mutation determines age at death but not disease duration in Huntington disease
JW Keum, A Shin, T Gillis, JS Mysore, KA Elneel, D Lucente, T Hadzi, ...
The American Journal of Human Genetics 98 (2), 287-298, 2016
1462016
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مقالات 1–20