Articles with public access mandates - Christine KleinLearn more
Not available anywhere: 122
Review
Pharmacological rescue of mitochondrial deficits in iPSC-derived neural cells from patients with familial Parkinson’s disease
O Cooper, H Seo, S Andrabi, C Guardia-Laguarta, J Graziotto, ...
Science translational medicine 4 (141), 141ra90-141ra90, 2012
Mandates: US National Institutes of Health
Review
LRRK2 in Parkinson disease: challenges of clinical trials
E Tolosa, M Vila, C Klein, O Rascol
Nature Reviews Neurology 16 (2), 97-107, 2020
Mandates: Banking Foundation "la Caixa", Government of Spain
Review
Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice
A Keller, A Westenberger, MJ Sobrido, M Garcia-Murias, A Domingo, ...
Nature genetics 45 (9), 1077-1082, 2013
Mandates: Swiss National Science Foundation, US National Institutes of Health, German …
Review
The genetics of Parkinson disease: implications for neurological care
C Klein, MG Schlossmacher
Nature clinical practice Neurology 2 (3), 136-146, 2006
Mandates: German Research Foundation
Review
A biological classification of Parkinson's disease: the SynNeurGe research diagnostic criteria
GU Höglinger, CH Adler, D Berg, C Klein, TF Outeiro, W Poewe, ...
The Lancet Neurology 23 (2), 191-204, 2024
Mandates: US National Institutes of Health, Canadian Institutes of Health Research …
Review
The many faces of alpha‐synuclein mutations
M Kasten, C Klein
Movement Disorders 28 (6), 697-701, 2013
Mandates: German Research Foundation
Review
ATP13A2 mutations impair mitochondrial function in fibroblasts from patients with Kufor-Rakeb syndrome
A Grünewald, B Arns, P Seibler, A Rakovic, A Münchau, A Ramirez, ...
Neurobiology of aging 33 (8), 1843. e1-1843. e7, 2012
Mandates: German Research Foundation
Review
The dystonia gene DYT1 is repressed by the transcription factor THAP1 (DYT6)
FJ Kaiser, A Osmanoric, A Rakovic, A Erogullari, N Uflacker, D Braunholz, ...
Annals of neurology 68 (4), 554-559, 2010
Mandates: German Research Foundation
Review
Genetics of Parkinson disease and other movement disorders
KR Kumar, K Lohmann, C Klein
Current opinion in neurology 25 (4), 466-474, 2012
Mandates: National Health and Medical Research Council, Australia, German Research …
Review
Hereditary parkinsonism: Parkinson disease look‐alikes—An algorithm for clinicians to “PARK” genes and beyond
C Klein, SA Schneider, AE Lang
Movement disorders: official journal of the Movement Disorder Society 24 (14 …, 2009
Mandates: Canadian Institutes of Health Research, German Research Foundation
Review
Substantia nigra hyperechogenicity correlates with clinical status and number of Parkin mutated alleles
JM Hagenah, IR König, B Becker, R Hilker, M Kasten, K Hedrich, ...
Journal of neurology 254, 1407-1413, 2007
Mandates: German Research Foundation
Review
Genetics of dystonia: what's known? What's new? What's next?
K Lohmann, C Klein
Movement Disorders 28 (7), 899-905, 2013
Mandates: German Research Foundation
Review
Next-Generation Phenotyping Using the Parkin Example: Time to Catch Up With Genetics
A Grünewald, M Kasten, A Ziegler, C Klein
JAMA neurology 70 (9), 2013
Mandates: German Research Foundation
Review
Childhood‐onset restless legs syndrome: Clinical and genetic features of 22 families
H Muhle, A Neumann, K Lohmann‐Hedrich, T Lohnau, Y Lu, S Winkler, ...
Movement Disorders: Official Journal of the Movement Disorder Society 23 (8 …, 2008
Mandates: German Research Foundation
Review
Myopathy causing camptocormia in idiopathic Parkinson's disease: a multidisciplinary approach
S Spuler, H Krug, C Klein, IC Medialdea, W Jakob, G Ebersbach, ...
Movement disorders 25 (5), 552-559, 2010
Mandates: German Research Foundation
Review
Whispering dysphonia in an Australian family (DYT4): a clinical and genetic reappraisal
RA Wilcox, S Winkler, K Lohmann, C Klein
Movement disorders 26 (13), 2404-2408, 2011
Mandates: German Research Foundation
Review
A heterozygous frameshift mutation in PRKRA (DYT16) associated with generalised dystonia in a German patient
P Seibler, A Djarmati, B Langpap, J Hagenah, A Schmidt, N Brüggemann, ...
The Lancet Neurology 7 (5), 380-381, 2008
Mandates: German Research Foundation
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
Progression of subtle motor signs in PINK1 mutation carriers with mild dopaminergic deficit
C Eggers, A Schmidt, J Hagenah, N Bruggemann, JC Klein, V Tadic, ...
Neurology 74 (22), 1798-1805, 2010
Mandates: German Research Foundation
Review
Impaired sense of smell and color discrimination in monogenic and idiopathic Parkinson's disease
L Kertelge, N Brüggemann, A Schmidt, V Tadic, C Wisse, S Dankert, ...
Movement disorders 25 (15), 2665-2669, 2010
Mandates: US National Institutes of Health, German Research Foundation
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