Articles with public access mandates - Thomas GasserLearn more
Not available anywhere: 38
Review
Milestones in PD genetics
T Gasser, J Hardy, Y Mizuno
Movement Disorders 26 (6), 1042-1048, 2011
Mandates: Parkinson's UK
Review
Changing the research criteria for the diagnosis of Parkinson's disease: obstacles and opportunities
D Berg, AE Lang, RB Postuma, W Maetzler, G Deuschl, T Gasser, ...
The Lancet Neurology 12 (5), 514-524, 2013
Mandates: Canadian Institutes of Health Research, Fonds de recherche du Québec - Santé …
Review
The tremor network targeted by successful VIM deep brain stimulation in humans
JC Klein, MT Barbe, C Seifried, S Baudrexel, M Runge, M Maarouf, ...
Neurology 78 (11), 787-795, 2012
Mandates: German Research Foundation
Review
Paroxysmal choreoathetosis/spasticity (DYT9) is caused by a GLUT1 defect
YG Weber, C Kamm, A Suls, J Kempfle, K Kotschet, R Schüle, TV Wuttke, ...
Neurology 77 (10), 959-964, 2011
Mandates: Research Foundation (Flanders), German Research Foundation
Review
Homo‐and heterodimerization of ROCO kinases: LRRK2 kinase inhibition by the LRRK2 ROCO fragment
CL Klein, G Rovelli, W Springer, C Schall, T Gasser, PJ Kahle
Journal of neurochemistry 111 (3), 703-715, 2009
Mandates: US National Institutes of Health
Review
Genome‐wide association study in musician's dystonia: A risk variant at the arylsulfatase G locus?
K Lohmann, A Schmidt, A Schillert, S Winkler, A Albanese, F Baas, ...
Movement Disorders 29 (7), 921-927, 2014
Mandates: German Research Foundation, Government of Spain, Government of Italy
Review
Enlarged hyperechogenic substantia nigra is related to motor performance and olfaction in the elderly
D Berg, K Seppi, I Liepelt, K Schweitzer, F Wollenweber, B Wolf, ...
Movement disorders 25 (10), 1464-1469, 2010
Mandates: German Research Foundation
Review
ATAXIA WITH OPHTHALMOPLEGIA OR SENSORY NEUROPATHY IS FREQUENTLY CAUSED BY POLG MUTATIONS
C Schulte, M Synofzik, T Gasser, L Schöls
Neurology 73 (11), 898-900, 2009
Mandates: German Research Foundation
Review
Deep-brain-stimulation does not impair deglutition in Parkinson's disease
S Lengerer, J Kipping, N Rommel, D Weiss, S Breit, T Gasser, C Plewnia, ...
Parkinsonism & related disorders 18 (7), 847-853, 2012
Mandates: German Research Foundation
Review
Delta‐like 1 participates in the specification of ventral midbrain progenitor derived dopaminergic neurons
M Bauer, J Szulc, M Meyer, CH Jensen, TA Terki, A Meixner, N Kinkl, ...
Journal of neurochemistry 104 (4), 1101-1115, 2008
Mandates: German Research Foundation
Review
RLS3: fine-mapping of an autosomal dominant locus in a family with intrafamilial heterogeneity
KM Liebetanz, J Winkelmann, C Trenkwalder, B Putz, M Dichgans, ...
Neurology 67 (2), 320-321, 2006
Mandates: German Research Foundation
Review
Rare variants in specific lysosomal genes are associated with Parkinson's disease
F Hopfner, SH Mueller, S Szymczak, O Junge, L Tittmann, S May, ...
Movement Disorders 35 (7), 1245-1248, 2020
Mandates: German Research Foundation
Review
Genetic factors influencing age at onset in LRRK2-linked Parkinson disease
Y Golub, D Berg, DB Calne, RF Pfeiffer, RJ Uitti, AJ Stoessl, ZK Wszolek, ...
Parkinsonism & related disorders 15 (7), 539-541, 2009
Mandates: US National Institutes of Health, Canadian Institutes of Health Research
Review
Reduction of susceptibility-induced signal losses in multi-gradient-echo images: application to improved visualization of the subthalamic nucleus
S Volz, E Hattingen, C Preibisch, T Gasser, R Deichmann
Neuroimage 45 (4), 1135-1143, 2009
Mandates: German Research Foundation
Review
The progressive supranuclear palsy clinical deficits scale
I Piot, K Schweyer, G Respondek, M Stamelou, DescribePSP study group, ...
Movement Disorders 35 (4), 650-661, 2020
Mandates: US National Institutes of Health, German Research Foundation, Federal …
Review
Dementia with lewy bodies: GBA1 mutations are associated with cerebrospinal fluid alpha‐synuclein profile
S Lerche, G Machetanz, I Wurster, B Roeben, M Zimmermann, A Pilotto, ...
Movement Disorders 34 (7), 1069-1073, 2019
Mandates: US National Institutes of Health, Helmholtz Association, European Commission …
Review
A novel homozygous DJ1 mutation causes parkinsonism and ALS in a Turkish family
HA Hanagasi, A Giri, E Kartal, G Guven, B Bilgiç, AK Hauser, M Emre, ...
Parkinsonism & related disorders 29, 117-120, 2016
Mandates: US National Institutes of Health, Fundação para a Ciência e a Tecnologia …
Review
Role of sepiapterin reductase gene at the PARK3 locus in Parkinson's disease
M Sharma, DM Maraganore, JPA Ioannidis, O Riess, JO Aasly, G Annesi, ...
Neurobiology of aging 32 (11), 2108. e1-2108. e5, 2011
Mandates: US National Institutes of Health, Research Foundation (Flanders)
Review
Cerebrospinal Fluid Progranulin, but Not Serum Progranulin, Is Reduced in GRN-Negative Frontotemporal Dementia
C Wilke, F Gillardon, C Deuschle, MA Hobert, IE Jansen, FG Metzger, ...
Neurodegenerative Diseases 17 (2-3), 83-88, 2017
Mandates: Federal Ministry of Education and Research, Germany
Review
A patient-based model of RNA mis-splicing uncovers treatment targets in Parkinson’s disease
I Boussaad, CD Obermaier, Z Hanss, DR Bobbili, S Bolognin, E Glaab, ...
Science translational medicine 12 (560), eaau3960, 2020
Mandates: US National Institutes of Health, German Research Foundation, Helmholtz …
Publication and funding information is determined automatically by a computer program