PUB - Publikationen an der Universität Bielefeld

Premotor Parkinson's disease: clinical features, detection, and prospects for treatment.
Siderowf A, Stern MB., Ann. Neurol. 64 Suppl 2(), 2008
PMID: 19127581

Predictors of phenotypic progression and disease onset in premanifest and early-stage Huntington's disease in the TRACK-HD study: analysis of 36-month observational data.
Tabrizi SJ, Scahill RI, Owen G, Durr A, Leavitt BR, Roos RA, Borowsky B, Landwehrmeyer B, Frost C, Johnson H, Craufurd D, Reilmann R, Stout JC, Langbehn DR; TRACK-HD Investigators, Campbell C, Campbell M, Labuschagne I, Milchman C, Coleman A, Dar Santos R, Decolongon J, Sturrock A, Jauffret C, Justo D, Lehericy S, Marelli C, Nigaud K, Valabregue R, Bechtel N, Bohlen S, van den Bogaard SJ, Dumas EM, van der Grond J, 't Hart EP, Arran N, Callaghan J, Stopford C, Cash DM, Crawford H, Fox NC, Hobbs NZ, Lahiri N, Malone I, Read J, Say MJ, Whitehead D, Wild E, Jones R, Axelson E, Queller S, Campbell C., Lancet Neurol 12(7), 2013
PMID: 23664844

Biological and clinical characteristics of individuals at risk for spinocerebellar ataxia types 1, 2, 3, and 6 in the longitudinal RISCA study: analysis of baseline data.
Jacobi H, Reetz K, du Montcel ST, Bauer P, Mariotti C, Nanetti L, Rakowicz M, Sulek A, Durr A, Charles P, Filla A, Antenora A, Schols L, Schicks J, Infante J, Kang JS, Timmann D, Di Fabio R, Masciullo M, Baliko L, Melegh B, Boesch S, Burk K, Peltz A, Schulz JB, Dufaure-Gare I, Klockgether T., Lancet Neurol 12(7), 2013
PMID: 23707147

The preclinical stage of spinocerebellar ataxias.
Maas RP, van Gaalen J, Klockgether T, van de Warrenburg BP., Neurology 85(1), 2015
PMID: 26062625

Progression of early features of spinocerebellar ataxia type 2 in individuals at risk: a longitudinal study.
Velazquez-Perez L, Rodriguez-Labrada R, Canales-Ochoa N, Montero JM, Sanchez-Cruz G, Aguilera-Rodriguez R, Almaguer-Mederos LE, Laffita-Mesa JM., Lancet Neurol 13(5), 2014
PMID: 24657153

Exercise and genetic rescue of SCA1 via the transcriptional repressor Capicua.
Fryer JD, Yu P, Kang H, Mandel-Brehm C, Carter AN, Crespo-Barreto J, Gao Y, Flora A, Shaw C, Orr HT, Zoghbi HY., Science 334(6056), 2011
PMID: 22053053

Scale for the assessment and rating of ataxia: development of a new clinical scale.
Schmitz-Hubsch T, du Montcel ST, Baliko L, Berciano J, Boesch S, Depondt C, Giunti P, Globas C, Infante J, Kang JS, Kremer B, Mariotti C, Melegh B, Pandolfo M, Rakowicz M, Ribai P, Rola R, Schols L, Szymanski S, van de Warrenburg BP, Durr A, Klockgether T, Fancellu R., Neurology 66(11), 2006
PMID: 16769946

Presymptomatic features of spinocerebellar ataxias.
Storey E., Lancet Neurol 12(7), 2013
PMID: 23707146

Early symptoms in spinocerebellar ataxia type 1, 2, 3, and 6.
Globas C, du Montcel ST, Baliko L, Boesch S, Depondt C, DiDonato S, Durr A, Filla A, Klockgether T, Mariotti C, Melegh B, Rakowicz M, Ribai P, Rola R, Schmitz-Hubsch T, Szymanski S, Timmann D, Van de Warrenburg BP, Bauer P, Schols L., Mov. Disord. 23(15), 2008
PMID: 18759344

Nystagmus as an early ocular alteration in Machado-Joseph disease (MJD/SCA3).
Raposo M, Vasconcelos J, Bettencourt C, Kay T, Coutinho P, Lima M., BMC Neurol 14(), 2014
PMID: 24450306

Clinical, neuropathologic, and genetic studies of a large spinocerebellar ataxia type 1 (SCA1) kindred: (CAG)n expansion and early premonitory signs and symptoms.
Genis D, Matilla T, Volpini V, Rosell J, Davalos A, Ferrer I, Molins A, Estivill X., Neurology 45(1), 1995
PMID: 7824128

The influence of focal cerebellar lesions on the control and adaptation of gait.
Ilg W, Giese MA, Gizewski ER, Schoch B, Timmann D., Brain 131(Pt 11), 2008
PMID: 18835866

Specific influences of cerebellar dysfunctions on gait.
Ilg W, Golla H, Thier P, Giese MA., Brain 130(Pt 3), 2007
PMID: 17287287

Gait ataxia--specific cerebellar influences and their rehabilitation.
Ilg W, Timmann D., Mov. Disord. 28(11), 2013
PMID: 24132845

Gait pattern in inherited cerebellar ataxias.
Serrao M, Pierelli F, Ranavolo A, Draicchio F, Conte C, Don R, Di Fabio R, LeRose M, Padua L, Sandrini G, Casali C., Cerebellum 11(1), 2012
PMID: 21717229

Increased gait variability is associated with the history of falls in patients with cerebellar ataxia.
Schniepp R, Wuehr M, Schlick C, Huth S, Pradhan C, Dieterich M, Brandt T, Jahn K., J. Neurol. 261(1), 2013
PMID: 24263407

Gait impairment precedes clinical symptoms in spinocerebellar ataxia type 6.
Rochester L, Galna B, Lord S, Mhiripiri D, Eglon G, Chinnery PF., Mov. Disord. 29(2), 2013
PMID: 24301795

Effects of cerebellar lesions on working memory interacting with motor tasks of different complexities.
Ilg W, Christensen A, Mueller OM, Goericke SL, Giese MA, Timmann D., J. Neurophysiol. 110(10), 2013
PMID: 23966680

Long-term effects of coordinative training in degenerative cerebellar disease.
Ilg W, Brotz D, Burkard S, Giese MA, Schols L, Synofzik M., Mov. Disord. 25(13), 2010
PMID: 20737551

Video game-based coordinative training improves ataxia in children with degenerative ataxia.
Ilg W, Schatton C, Schicks J, Giese MA, Schols L, Synofzik M., Neurology 79(20), 2012
PMID: 23115212

Intensive coordinative training improves motor performance in degenerative cerebellar disease.
Ilg W, Synofzik M, Brotz D, Burkard S, Giese MA, Schols L., Neurology 73(22), 2009
PMID: 19864636

Videogame-based coordinative training can improve advanced, multisystemic early-onset ataxia.
Synofzik M, Schatton C, Giese M, Wolf J, Schols L, Ilg W., J. Neurol. 260(10), 2013
PMID: 23989345

Spinocerebellar ataxia types 1, 2, 3 and 6: the clinical spectrum of ataxia and morphometric brainstem and cerebellar findings.
Jacobi H, Hauser TK, Giunti P, Globas C, Bauer P, Schmitz-Hubsch T, Baliko L, Filla A, Mariotti C, Rakowicz M, Charles P, Ribai P, Szymanski S, Infante J, van de Warrenburg BP, Durr A, Timmann D, Boesch S, Fancellu R, Rola R, Depondt C, Schols L, Zdzienicka E, Kang JS, Ratzka S, Kremer B, Stephenson DA, Melegh B, Pandolfo M, Tezenas du Montcel S, Borkert J, Schulz JB, Klockgether T., Cerebellum 11(1), 2012
PMID: 21701895

Clinical assessment of balance: normative data, and gender and age effects.
Vereeck L, Wuyts F, Truijen S, Van de Heyning P., Int J Audiol 47(2), 2008
PMID: 18236239

Gait characteristics and sensory abilities of older adults are modulated by gender.
Scaglioni-Solano P, Aragon-Vargas LF., Gait Posture 42(1), 2015
PMID: 25943408

Spinocerebellar ataxia types 1, 2, 3, and 6: disease severity and nonataxia symptoms.
Schmitz-Hubsch T, Coudert M, Bauer P, Giunti P, Globas C, Baliko L, Filla A, Mariotti C, Rakowicz M, Charles P, Ribai P, Szymanski S, Infante J, van de Warrenburg BP, Durr A, Timmann D, Boesch S, Fancellu R, Rola R, Depondt C, Schols L, Zdienicka E, Kang JS, Dohlinger S, Kremer B, Stephenson DA, Melegh B, Pandolfo M, di Donato S, du Montcel ST, Klockgether T., Neurology 71(13), 2008
PMID: 18685131

Prediction of the age at onset in spinocerebellar ataxia type 1, 2, 3 and 6.
Tezenas du Montcel S, Durr A, Rakowicz M, Nanetti L, Charles P, Sulek A, Mariotti C, Rola R, Schols L, Bauer P, Dufaure-Gare I, Jacobi H, Forlani S, Schmitz-Hubsch T, Filla A, Timmann D, van de Warrenburg BP, Marelli C, Kang JS, Giunti P, Cook A, Baliko L, Melegh B, Bela M, Boesch S, Szymanski S, Berciano J, Infante J, Buerk K, Masciullo M, Di Fabio R, Depondt C, Ratka S, Stevanin G, Klockgether T, Brice A, Golmard JL., J. Med. Genet. 51(7), 2014
PMID: 24780882

Spinocerebellar ataxia type 2: polyQ repeat variation in the CACNA1A calcium channel modifies age of onset.
Pulst SM, Santos N, Wang D, Yang H, Huynh D, Velazquez L, Figueroa KP., Brain 128(Pt 10), 2005
PMID: 16000334

Age at onset variance analysis in spinocerebellar ataxias: a study in a Dutch-French cohort.
van de Warrenburg BP, Hendriks H, Durr A, van Zuijlen MC, Stevanin G, Camuzat A, Sinke RJ, Brice A, Kremer BP., Ann. Neurol. 57(4), 2005
PMID: 15747371

Modulation of the age at onset in spinocerebellar ataxia by CAG tracts in various genes.
Tezenas du Montcel S, Durr A, Bauer P, Figueroa KP, Ichikawa Y, Brussino A, Forlani S, Rakowicz M, Schols L, Mariotti C, van de Warrenburg BP, Orsi L, Giunti P, Filla A, Szymanski S, Klockgether T, Berciano J, Pandolfo M, Boesch S, Melegh B, Timmann D, Mandich P, Camuzat A; Clinical Research Consortium for Spinocerebellar Ataxia (CRC-SCA); EUROSCA network, Goto J, Ashizawa T, Cazeneuve C, Tsuji S, Pulst SM, Brusco A, Riess O, Brice A, Stevanin G, Ashizawa T, Figueroa K, Perlman S, Gomez C, Wilmot G, Schmahmann J, Ying SH, Zesiewicz T, Paulson H, Shakkottai V, Bushara K, Kuo SH, Geschwind M, Xia G, Mazzoni P, Pulst S, Subramony S, du Montcel ST, Durr A, Bauer P, Forlani S, Rakowicz M, Sulek A, Schols L, Mariotti C, van de Warrenburg BP, Giunti P, Filla A, Szymanski S, Klockgether T, Berciano J, Pandolfo M, Boesch S, Bela M, Baliko L, Hadzsiev K, Timmann D, Riess O, Brice A, Stevanin G., Brain 137(Pt 9), 2014
PMID: 24972706

Winter, 1991

Bishop, 2006

Hastie, 2009

International Cooperative Ataxia Rating Scale for pharmacological assessment of the cerebellar syndrome. The Ataxia Neuropharmacology Committee of the World Federation of Neurology.
Trouillas P, Takayanagi T, Hallett M, Currier RD, Subramony SH, Wessel K, Bryer A, Diener HC, Massaquoi S, Gomez CM, Coutinho P, Ben Hamida M, Campanella G, Filla A, Schut L, Timann D, Honnorat J, Nighoghossian N, Manyam B., J. Neurol. Sci. 145(2), 1997
PMID: 9094050

SCA Functional Index: a useful compound performance measure for spinocerebellar ataxia.
Schmitz-Hubsch T, Giunti P, Stephenson DA, Globas C, Baliko L, Sacca F, Mariotti C, Rakowicz M, Szymanski S, Infante J, van de Warrenburg BP, Timmann D, Fancellu R, Rola R, Depondt C, Schols L, Zdzienicka E, Kang JS, Dohlinger S, Kremer B, Melegh B, Filla A, Klockgether T., Neurology 71(7), 2008
PMID: 18695159

Motor decline in clinically presymptomatic spinocerebellar ataxia type 2 gene carriers.
Velazquez-Perez L, Diaz R, Perez-Gonzalez R, Canales N, Rodriguez-Labrada R, Medrano J, Sanchez G, Almaguer-Mederos L, Torres C, Fernandez-Ruiz J., PLoS ONE 4(4), 2009
PMID: 19401771

AUTHOR UNKNOWN, 0

Gait alterations in healthy carriers of the LRRK2 G2019S mutation.
Mirelman A, Gurevich T, Giladi N, Bar-Shira A, Orr-Urtreger A, Hausdorff JM., Ann. Neurol. 69(1), 2011
PMID: 21280089

Characterization and Early Detection of Balance Deficits in Fragile X Premutation Carriers With and Without Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS).
O'Keefe JA, Robertson-Dick E, Dunn EJ, Li Y, Deng Y, Fiutko AN, Berry-Kravis E, Hall DA., Cerebellum 14(6), 2015
PMID: 25763861

Gait and Functional Mobility Deficits in Fragile X-Associated Tremor/Ataxia Syndrome.
O'Keefe JA, Robertson-Dick EE, Hall DA, Berry-Kravis E., Cerebellum 15(4), 2016
PMID: 26298472

Long-term disease progression in spinocerebellar ataxia types 1, 2, 3, and 6: a longitudinal cohort study.
Jacobi H, du Montcel ST, Bauer P, Giunti P, Cook A, Labrum R, Parkinson MH, Durr A, Brice A, Charles P, Marelli C, Mariotti C, Nanetti L, Panzeri M, Rakowicz M, Sulek A, Sobanska A, Schmitz-Hubsch T, Schols L, Hengel H, Baliko L, Melegh B, Filla A, Antenora A, Infante J, Berciano J, van de Warrenburg BP, Timmann D, Szymanski S, Boesch S, Kang JS, Pandolfo M, Schulz JB, Molho S, Diallo A, Klockgether T., Lancet Neurol 14(11), 2015
PMID: 26377379