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Results 1 to 9 of 9

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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

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

PINK1, Parkin, and DJ-1 mutations in Italian patients with early-onset parkinsonismKLEIN, Christine; DJARMATI, Ana; WINKLER, Susen et al.European journal of human genetics. 2005, Vol 13, Num 9, pp 1086-1093, issn 1018-4813, 8 p.Article

Genetic risk factors in Parkinson's disease: single gene effects and interactions of genotypesGÖBEL, Anna; MACKLIN, Eric A; WINKLER, Susen et al.Journal of neurology. 2012, Vol 259, Num 11, pp 2503-2505, issn 0340-5354, 3 p.Article

Recurrent LRRK2 (Park8) mutations in early-onset parkinson's diseaseHEDRICH, Katja; WINKLER, Susen; KLEIN, Christine et al.Movement disorders. 2006, Vol 21, Num 9, pp 1506-1510, issn 0885-3185, 5 p.Article

Identification and functional analysis of novel THAP1 mutationsLOHMANN, Katja; UFLACKER, Nils; ZITTEL, Simone et al.European journal of human genetics. 2012, Vol 20, Num 2, pp 171-175, issn 1018-4813, 5 p.Article

ATP13A2 Variants in Early-Onset Parkinson's Disease Patients and ControlsDJARMATI, Ana; HAGENAH, Johann; BERG, Daniela et al.Movement disorders. 2009, Vol 24, Num 14, pp 2104-2111, issn 0885-3185, 8 p.Article

Childhood-onset Restless Legs Syndrome : Clinical and Genetic Features of 22 FamiliesMUHLE, Hiltrud; NEUMANN, Anja; STEPHANI, Ulrich et al.Movement disorders. 2008, Vol 23, Num 8, pp 1113-1121, issn 0885-3185, 9 p.Article

Myoclonus-Dystonia Due to Maternal Uniparental DisomyGUETTARD, Emilie; PORTNOI, Marie-France; KLEIN, Christine et al.Archives of neurology (Chicago). 2008, Vol 65, Num 10, pp 1380-1385, issn 0003-9942, 6 p.Article

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