Các bài viết có thể truy cập công khai - Patrick WeydtTìm hiểu thêm
Không có ở bất kỳ nơi nào: 14
Neurofilament levels as biomarkers in asymptomatic and symptomatic familial amyotrophic lateral sclerosis
P Weydt, P Oeckl, A Huss, K Müller, AE Volk, J Kuhle, A Knehr, ...
Annals of neurology 79 (1), 152-158, 2016
Các cơ quan ủy nhiệm: Helmholtz Association
Hypothalamic atrophy is related to body mass index and age at onset in amyotrophic lateral sclerosis
M Gorges, P Vercruysse, HP Müller, HJ Huppertz, A Rosenbohm, G Nagel, ...
Journal of Neurology, Neurosurgery & Psychiatry 88 (12), 1033-1041, 2017
Các cơ quan ủy nhiệm: German Research Foundation, Helmholtz Association, Fondazione Telethon …
Serum microRNAs in sporadic amyotrophic lateral sclerosis
A Freischmidt, K Müller, L Zondler, P Weydt, B Mayer, CAF von Arnim, ...
Neurobiology of aging 36 (9), 2660. e15-2660. e20, 2015
Các cơ quan ủy nhiệm: German Research Foundation
ALS-causing mutations differentially affect PGC-1α expression and function in the brain vs. peripheral tissues
H Bayer, K Lang, E Buck, J Higelin, L Barteczko, N Pasquarelli, J Sprissler, ...
Neurobiology of disease 97, 36-45, 2017
Các cơ quan ủy nhiệm: German Research Foundation, Helmholtz Association
Contrasting effects of selective MAGL and FAAH inhibition on dopamine depletion and GDNF expression in a chronic MPTP mouse model of Parkinson's disease
N Pasquarelli, C Porazik, H Bayer, E Buck, S Schildknecht, P Weydt, ...
Neurochemistry International 110, 14-24, 2017
Các cơ quan ủy nhiệm: German Research Foundation
Evaluation of monoacylglycerol lipase as a therapeutic target in a transgenic mouse model of ALS
N Pasquarelli, M Engelskirchen, J Hanselmann, S Endres, C Porazik, ...
Neuropharmacology 124, 157-169, 2017
Các cơ quan ủy nhiệm: German Research Foundation, Helmholtz Association
The concept and diagnostic criteria of primary lateral sclerosis
V Wais, A Rosenbohm, S Petri, K Kollewe, A Hermann, A Storch, ...
Acta Neurologica Scandinavica 136 (3), 204-211, 2017
Các cơ quan ủy nhiệm: German Research Foundation
The metabolic and endocrine characteristics in spinal and bulbar muscular atrophy
A Rosenbohm, S Hirsch, AE Volk, T Grehl, J Grosskreutz, F Hanisch, ...
Journal of neurology 265, 1026-1036, 2018
Các cơ quan ủy nhiệm: Federal Ministry of Education and Research, Germany
Can lesions to the motor cortex induce amyotrophic lateral sclerosis?
A Rosenbohm, J Kassubek, P Weydt, N Marroquin, AE Volk, C Kubisch, ...
Journal of neurology 261, 283-290, 2014
Các cơ quan ủy nhiệm: German Research Foundation
Clinical trials in spinal and bulbar muscular atrophy—past, present, and future
P Weydt, A Sagnelli, A Rosenbohm, P Fratta, PF Pradat, AC Ludolph, ...
Journal of Molecular Neuroscience 58, 379-387, 2016
Các cơ quan ủy nhiệm: Motor Neurone Disease Association, UK, UK Medical Research Council
Towards a European registry and biorepository for patients with spinal and bulbar muscular atrophy
D Pareyson, P Fratta, PF Pradat, G Sorarù, J Finsterer, J Vissing, ...
Journal of Molecular Neuroscience 58, 394-400, 2016
Các cơ quan ủy nhiệm: Fondazione Telethon, Italy, Motor Neurone Disease Association, UK, UK …
The psychopharmacology of Huntington disease
Å Petersén, P Weydt
Handbook of Clinical Neurology 165, 179-189, 2019
Các cơ quan ủy nhiệm: Swedish Research Council
Theme 06-Tissue Biomarkers.
Y Bobeva, S Castro-Gomez, N Kittipeerapat, M Heneka, P Weydt, N Gaur, ...
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration 23 (1), 2022
Các cơ quan ủy nhiệm: Swedish Research Council, European Commission, Government of Spain
B30 Integrated mitochondrial function in human fine-needle muscle biopsies of huntington’s disease mutation carriers and in tissues of HdhQ111 mice
E Buck, T Merz, A Gumpp, A Witting, J Steinacker, M Zügel, U Schumann, ...
Journal of Neurology, Neurosurgery & Psychiatry 87 (Suppl 1), A19-A20, 2016
Các cơ quan ủy nhiệm: German Research Foundation
Có tại một số nơi: 46
Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia
A Freischmidt, T Wieland, B Richter, W Ruf, V Schaeffer, K Müller, ...
Nature neuroscience 18 (5), 631-636, 2015
Các cơ quan ủy nhiệm: German Research Foundation, Swedish Research Council
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
Các cơ quan ủy nhiệm: US National Institutes of Health, Government of Spain
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
Các cơ quan ủy nhiệm: UK Medical Research Council, National Institute for Health Research, UK …
Targeting neuroinflammation to treat Alzheimer’s disease
A Ardura-Fabregat, E Boddeke, A Boza-Serrano, S Brioschi, ...
CNS drugs 31, 1057-1082, 2017
Các cơ quan ủy nhiệm: US National Institutes of Health
Hot-spot KIF5A mutations cause familial ALS
D Brenner, R Yilmaz, K Müller, T Grehl, S Petri, T Meyer, J Grosskreutz, ...
Brain 141 (3), 688-697, 2018
Các cơ quan ủy nhiệm: US National Institutes of Health, German Research Foundation, Knut and Alice …
Multicenter evaluation of neurofilaments in early symptom onset amyotrophic lateral sclerosis
E Feneberg, P Oeckl, P Steinacker, F Verde, C Barro, P Van Damme, ...
Neurology 90 (1), e22-e30, 2018
Các cơ quan ủy nhiệm: Motor Neurone Disease Association, UK, UK Medical Research Council, Federal …
Chương trình máy tính sẽ tự động xác định thông tin xuất bản và thông tin về nhà tài trợ