Implications of genetics on the diagnosis and care of patients with parkinson diseaseKLEIN, Christine.Archives of neurology (Chicago). 2006, Vol 63, Num 3, pp 328-334, issn 0003-9942, 7 p.Article

Parkinson disease, 10 years after its genetic revolution : Multiple clues to a complex disorderKLEIN, Christine; SCHLOSSMACHER, Michael G.Neurology. 2007, Vol 69, Num 22, pp 2093-2104, issn 0028-3878, 12 p.Article

Clinical and Demographic Characteristics of PINK1 Mutation Carriers: A Meta-AnalysisKASTEN, Meike; WEICHERT, Charlotte; LOHMANN, Katja et al.Movement disorders. 2010, Vol 25, Num 7, pp 952-954, issn 0885-3185, 3 p.Article

Hereditary Parkinsonism: Parkinson Disease Look-Alikes: An Algorithm for Clinicians to PARK Genes and BeyondKLEIN, Christine; SCHNEIDER, Susanne A; LANG, Anthony E et al.Movement disorders. 2009, Vol 24, Num 14, pp 2042-2058, issn 0885-3185, 17 p.Article

Fixing the broken system of genetic locus symbols: Parkinson disease and dystonia as examplesMARRAS, Connie; LOHMANN, Katja; LANG, Anthony et al.Neurology. 2012, Vol 78, Num 13, pp 1016-1024, issn 0028-3878, 9 p.Article

Frequency of the D620N Mutation in VPS35 in Parkinson DiseaseKUMAR, Kishore R; WEISSBACH, Anne; SIMON, David K et al.Archives of neurology (Chicago). 2012, Vol 69, Num 10, pp 1360-1364, issn 0003-9942, 5 p.Article

Phenotypes and genetic architecture of focal primary torsion dystoniaGROEN, Justus L; KALLEN, Marlot C; BAAS, Frank et al.Journal of neurology, neurosurgery and psychiatry. 2012, Vol 83, Num 10, pp 1006-1011, issn 0022-3050, 6 p.Article

Neuropsychiatric symptoms and intelligence quotient in autosomal dominant Segawa diseaseLOPEZ-LASO, Eduardo; SANCHEZ-RAYA, Araceli; KLEIN, Christine et al.Journal of neurology. 2011, Vol 258, Num 12, pp 2155-2162, issn 0340-5354, 8 p.Article

Development and validation status of the IFMIF High Flux Test ModuleARBEITER, Frederik; ABOU-SENA, Ali; YUMING CHEN et al.Fusion engineering and design. 2011, Vol 86, Num 6-8, pp 607-610, issn 0920-3796, 4 p.Conference Paper

Clinical Neuroimaging and Electrophysiological Assessment of Three DYT6 Dystonia FamiliesZITTEL, Simone; MOLL, Christian K. E; SCHÖNWEILER, Rainer et al.Movement disorders. 2010, Vol 25, Num 14, pp 2405-2412, issn 0885-3185, 8 p.Article

Distinct Basal Ganglia Hyperechogenicity in Idiopathic Basal Ganglia CalcificationBRÜGGEMANN, Norbert; SCHNEIDER, Susanne A; SANDER, Thurid et al.Movement disorders. 2010, Vol 25, Num 15, pp 2661-2664, issn 0885-3185, 4 p.Article

Motor Complications in Patients Form the German Competence Network on Parkinson's Disease and the DRD3 Ser9Gly PolymorphismPAUS, Sebastian; GADOW, Franziska; KNAPP, Michael et al.Movement disorders. 2009, Vol 24, Num 7, pp 1080-1084, issn 0885-3185, 5 p.Article

The phenotypic spectrum of rapid-onset dystonia-parkinsonism (RDP) and mutations in the ATPIA3 geneBRASHEAR, Allison; DOBYNS, William B; LINAZASORO, Gurutz et al.Brain. 2007, Vol 130, pp 828-835, issn 0006-8950, 8 p., 3Article

Heterozygous PINK1 mutations : A susceptibility factor for parkinson disease?DJARMATI, Ana; HEDRICH, Katja; SVETEL, Marina et al.Movement disorders. 2006, Vol 21, Num 9, pp 1526-1530, issn 0885-3185, 5 p.Article

Clinical characteristics of paroxysmal nonkinesigenic dyskinesia in Serbian family with Myofibrillogenesis Regulator 1 gene mutationSTEFANOVA, Elka; DJARMATI, Ana; MOMCILOVIC, Dragana et al.Movement disorders. 2006, Vol 21, Num 11, pp 2010-2015, issn 0885-3185, 6 p.Article

[¹⁸F]-dopa positron emission tomography imaging in early-stage, non-parkin juvenile parkinsonismPAL, Pramod K; LEUNG, Joanne; HEDRICH, Katya et al.Movement disorders. 2002, Vol 17, Num 4, pp 789-794, issn 0885-3185Article

ε-Sarcoglycan mutations found in combination with other dystonia gene mutationsKLEIN, Christine; LIU LIU; SMITH, Christopher et al.Annals of neurology. 2002, Vol 52, Num 5, pp 675-679, issn 0364-5134, 5 p.Article

The importance of gene dosage studies : mutational analysis of the Parkin gene in early-onset parkinsonismHEDRICH, Katja; KANN, Martin; OZELIUS, Laurie J et al.Human molecular genetics (Print). 2001, Vol 10, Num 16, pp 1649-1656, issn 0964-6906Article

Global investigation and meta-analysis of the C9orf72 (G₄C₂)_n repeat in Parkinson diseaseTHEUNS, Jessie; VERSTRAETEN, Aline; KRÜGER, Rejko et al.Neurology. 2014, Vol 83, Num 21, pp 1906-1913, issn 0028-3878, 8 p.Article

Cohort Profile: A population-based cohort to study non-motor symptoms in parkinsonism (EPIPARK)KASTEN, Meike; HAGENAH, Johann; GRAF, Julia et al.International journal of epidemiology. 2013, Vol 42, Num 1, issn 0300-5771, p. 128Article

Two Faces of the Same Coin: Benign Familial Infantile Seizures and Paroxysmal Kinesigenic Dyskinesia Caused by PRRT2 MutationsSCHMIDT, Alexander; KUMAR, Kishore R; CHRISTEN, Hans-Jürgen et al.Archives of neurology (Chicago). 2012, Vol 69, Num 5, pp 668-670, issn 0003-9942, 3 p.Article

Musician's Dystonia and Comorbid Anxiety: Two Sides of One Coin?ENDERS, Leonie; SPECTOR, June T; ALTENMÜLLER, Eckart et al.Movement disorders. 2011, Vol 26, Num 3, pp 539-542, issn 0885-3185, 4 p.Article

Whispering Dysphonia in an Australian Family (DYT4): A Clinical and Genetic ReappraisalWILCOX, Robert A; WINKLER, Susen; LOHMANN, Katja et al.Movement disorders. 2011, Vol 26, Num 13, pp 2404-2408, issn 0885-3185, 5 p.Article

LINGO1 Is Not Associated With Parkinson's Disease in German PatientsKLEBE, Stephan; THIER, Sandra; GASSER, Thomas et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2010, Vol 153, Num 6, pp 1173-1178, issn 1552-4841, 6 p.Article

Nonmotor Symptoms in Parkin Gene-Related ParkinsonismKÄGI, Georg; KLEIN, Christine; WOOD, Nicholas W et al.Movement disorders. 2010, Vol 25, Num 9, pp 1279-1284, issn 0885-3185, 6 p.Article