POLG, but not PEO1, is a Frequent Cause of Cerebellar Ataxia in Central EuropeSCHICKS, Julia; SYNOFZIK, Matthis; SCHULTE, Claudia et al.Movement disorders. 2010, Vol 25, Num 15, pp 2678-2682, issn 0885-3185, 5 p.Article

ATAXIA WITH OPHTHALMOPLEGIA OR SENSORY NEUROPATHY IS FREQUENTLY CAUSED BY POLG MUTATIONSSCHULTE, Claudia; SYNOFZIK, Matthis; GASSER, Thomas et al.Neurology. 2009, Vol 73, Num 11, pp 898-900, issn 0028-3878, 3 p.Article

Late onset vanishing white matter diseaseRIECKER, Axel; NÄGELE, Thomas; HENNEKE, Marco et al.Journal of neurology. 2007, Vol 254, Num 4, pp 544-545, issn 0340-5354, 2 p.Article

Idebenone in patients with Friedreich ataxiaSCHÖLS, Ludger; VORGERD, Matthias; SCHILLINGS, Monika et al.Neuroscience letters. 2001, Vol 306, Num 3, pp 169-172, issn 0304-3940Article

Severe orthostatic dysregulation associated with Wolfram syndromeSYNOFZIK, Matthis; WEISS, Daniel; ERHARHAGHEN, Jite et al.Journal of neurology. 2010, Vol 257, Num 10, pp 1751-1753, issn 0340-5354, 3 p.Article

Axonal transport deficit in a KIF5A^-/- mouse modelKARLE, Kathrin N; MÖCKEL, Diana; REID, Evan et al.Neurogenetics (Oxford. Print). 2012, Vol 13, Num 2, pp 169-179, issn 1364-6745, 11 p.Article

Identification and characterisation of a large Senataxin (SETX) gene duplication in ataxia with ocular apraxia type 2 (AOA2)ARNING, Larissa; SCHÖLS, Ludger; CIN, Huriye et al.Neurogenetics (Oxford. Print). 2008, Vol 9, Num 4, pp 295-299, issn 1364-6745, 5 p.Article

Complex Hyperkinetic Movement Disorders Associated with POLG MutationsSYNOFZIK, Matthis; SCHÜLE, Rebecca; SCHULTE, Claudia et al.Movement disorders. 2010, Vol 25, Num 14, pp 2472-2475, issn 0885-3185, 4 p.Article

Effect of spastic paraplegia mutations in KIF5A kinesin on transport activityEBBING, Bettina; MANN, Klaudiusz; STAROSTA, Agata et al.Human molecular genetics (Print). 2008, Vol 17, Num 9, pp 1245-1252, issn 0964-6906, 8 p.Article

Atypical Juvenile Parkinsonism in a Consanguineous SPG15 FamilySCHICKS, Julia; SYNOFZIK, Matthis; PETURSSON, Hjörvar et al.Movement disorders. 2011, Vol 26, Num 3, pp 564-566, issn 0885-3185, 3 p.Article

Long-Term Effects of Coordinative Training in Degenerative Cerebellar DiseaseILG, Winfried; BRÖTZ, Doris; BURKARD, Susanne et al.Movement disorders. 2010, Vol 25, Num 13, pp 2239-2246, issn 0885-3185, 8 p.Article

Pseudodominant inheritance of ataxia with ocular apraxia type 2 (AOA2)SCHÖLS, Ludger; ARNING, Larissa; SCHIILE, Rebecca et al.Journal of neurology. 2008, Vol 255, Num 4, pp 495-501, issn 0340-5354, 7 p.Article

POLG and PEO1 (Twinkle) mutations are infrequent in PSP-like atypical parkinsonism: a preliminary screening studySYNOFZIK, Matthis; SCHICKS, Julia; SRULIJES, Karin et al.Journal of neurology. 2012, Vol 259, Num 10, pp 2232-2233, issn 0340-5354, 2 p.Article

The human G93A SOD1 phenotype closely resembles sporadic amyotrophic lateral sclerosisSYNOFZIK, Matthis; FERNANDEZ-SANTIAGO, Rubén; MAETZLER, Walter et al.Journal of neurology, neurosurgery and psychiatry. 2010, Vol 81, Num 7, pp 764-767, issn 0022-3050, 4 p.Article

Polymorphisms in the interleukin-1 alpha and beta genes and the risk for Parkinson's diseaseSCHULTE, Thorsten; SCHÖLS, Ludger; MÜLLER, Thomas et al.Neuroscience letters. 2002, Vol 326, Num 1, pp 70-72, issn 0304-3940Article

Neurofilament L gene is not a genetic factor of sporadic and familial Parkinson's diseaseRAHNER, Nils; HOLZMANN, Carsten; KRÜGER, Rejko et al.Brain research. 2002, Vol 951, Num 1, pp 82-86, issn 0006-8993Article

Video game―based coordinative training improves ataxia in children with degenerative ataxiaILG, Winfried; SCHATTON, Cornelia; SCHICKS, Julia et al.Neurology. 2012, Vol 79, Num 20, pp 2056-2060, issn 0028-3878, 5 p.Article

Spinal cord atrophy in spinocerebellar ataxia type 3 and 6 : Impact on clinical disabilityLUKAS, Carsten; HAHN, Horst K; BELLENBERG, Barbara et al.Journal of neurology. 2008, Vol 255, Num 8, pp 1244-1249, issn 0340-5354, 6 p.Article

Mutations in TITF1 are not relevant to sporadic and familial chorea of unknown causeBAUER, Peter; KREUZ, Friedmar R; BÜRK, Katrin et al.Movement disorders. 2006, Vol 21, Num 10, pp 1734-1737, issn 0885-3185, 4 p.Article

Loss of Nocturnal Blood Pressure Fall in Various Extrapyramidal SyndromesSCHMIDT, Claudia; BERG, Daniela; HERTING et al.Movement disorders. 2009, Vol 24, Num 14, pp 2136-2142, issn 0885-3185, 7 p.Article

Evaluation of the γ-synuclein gene in German Parkinson's disease patientsKRÜGER, Rejko; SCHÖLS, Ludger; MÜLLER, Thomas et al.Neuroscience letters. 2001, Vol 310, Num 2-3, pp 191-193, issn 0304-3940Article

Data protection in biomaterial banks for parkinson's disease research : The model of GEPARD (Gene bank parkinson's disease Germany)EGGERT, Karla; WÜLLNER, Ullrich; ANTONY, Gisela et al.Movement disorders. 2007, Vol 22, Num 5, pp 611-618, issn 0885-3185, 8 p.Article

CAG repeats in restless legs syndromeKONIECZNY, Markus; BAUER, Peter; TOMIUK, Jürgen et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2006, Vol 141, Num 2, pp 173-176, issn 1552-4841, 4 p.Article

Dissociation of grey and white matter reduction in spinocerebellar ataxia type 3 and 6 : A voxel- based morphometry studyLUKAS, Carsten; SCHÖLS, Ludger; BELLENBERG, Barbara et al.Neuroscience letters. 2006, Vol 408, Num 3, pp 230-235, issn 0304-3940, 6 p.Article

Association of moderate polyglutamine tract expansions in the slow calcium-activated potassium channel type 3 with ataxiaFIGUEROA, Karla Patricia; CHAN, Piu; SCHÖLS, Ludger et al.Archives of neurology (Chicago). 2001, Vol 58, Num 10, pp 1649-1653, issn 0003-9942Article