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Katrin Bürk

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Katrin Bürk; Karla P Figueroa; Hajo M Hamer; Wolfgang H Oertel; Stefan M Pulst; Philipp S Reif; Adam Strzelczyk; Christine Zühlke; Felix Rosenow
Mesial temporal lobe epilepsy in a patient with spinocerebellar ataxia type 13 (SCA13).
Udo Rüb; Ludger Schöls; Stephan W Schwarzacher; Kay Seidel; D Timmann; Jürgen R E Bohl; A Bornemann; E Brunt; Katrin Bürk; Wilfred F A den Dunnen; R Egensperger; K Farrag; Helmut Heinsen; Horst-Werner Korf; Thomas Deller
Spinocerebellar ataxia type 1 (SCA1): new pathoanatomical and clinico-pathological insights.
W Scherzed; Ludger Schöls; Kay Seidel; Georg Auburger; Ewout R Brunt; Katrin Bürk; Rob A I de Vos; Domenico Del Turco; Thomas Deller; Wilfred F A den Dunnen; Helmut Heinsen; Horst-Werner Korf; Udo Rüb
Pathoanatomy of cerebellar degeneration in spinocerebellar ataxia type 2 (SCA2) and type 3 (SCA3).

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All Publications

2013: Katrin Bürk; Karla P Figueroa; Hajo M Hamer; Wolfgang H Oertel; Stefan M Pulst; Philipp S Reif; Adam Strzelczyk; Christine Zühlke; Felix Rosenow
Mesial temporal lobe epilepsy in a patient with spinocerebellar ataxia type 13 (SCA13).
The International journal of neuroscience 2013;123(4):278-82.
2012: Udo Rüb; Ludger Schöls; Stephan W Schwarzacher; Kay Seidel; D Timmann; Jürgen R E Bohl; A Bornemann; E Brunt; Katrin Bürk; Wilfred F A den Dunnen; R Egensperger; K Farrag; Helmut Heinsen; Horst-Werner Korf; Thomas Deller
Spinocerebellar ataxia type 1 (SCA1): new pathoanatomical and clinico-pathological insights.
Neuropathology and applied neurobiology 2012;38(7):665-80.
2012: W Scherzed; Ludger Schöls; Kay Seidel; Georg Auburger; Ewout R Brunt; Katrin Bürk; Rob A I de Vos; Domenico Del Turco; Thomas Deller; Wilfred F A den Dunnen; Helmut Heinsen; Horst-Werner Korf; Udo Rüb
Pathoanatomy of cerebellar degeneration in spinocerebellar ataxia type 2 (SCA2) and type 3 (SCA3).
Cerebellum (London, England) 2012;11(3):749-60.
2011: Christine Zühlke; Friedmar R Kreuz; Katrin Bürk
[Clinical details and genetics of recessive ataxias].
Der Nervenarzt 2011;82(4):447-8, 450-8.
2011: Adam Strzelczyk; Katrin Bürk; Wolfgang H Oertel
Treatment of paroxysmal dyskinesias.
Expert opinion on pharmacotherapy 2011;12(1):63-72.
2010: Michel Mittelbronn; Jens Schittenhelm; Gellert Bakos; Rob A I de Vos; Manfred Wehrmann; Richard Meyermann; Katrin Bürk
CD8(+)/perforin/granzyme B(+) effector cells infiltrating cerebellum and inferior olives in gluten ataxia.
Neuropathology : official journal of the Japanese Society of Neuropathology 2010;30(1):92-6.
2010: Katrin Bürk; M Wick; G Roth; P Decker; R Voltz
Antineuronal antibodies in sporadic late-onset cerebellar ataxia.
Journal of neurology 2010;257(1):59-62.
2009: Katrin Bürk; Marie-Louise Farecki; Georg Lamprecht; Guenter Roth; Patrice Decker; Michael Weller; Hans-Georg Rammensee; Wolfang Oertel
Neurological symptoms in patients with biopsy proven celiac disease.
Movement disorders : official journal of the Movement Disorder Society 2009;24(16):2358-62.
2009: Veronica Bernard; Martina Minnerop; Katrin Bürk; Friedmar R Kreuz; Gabriele Gillessen-Kaesbach; Christine Zühlke
Exon deletions and intragenic insertions are not rare in ataxia with oculomotor apraxia 2.
BMC medical genetics 2009;10():87.
2008: F Hoche; Kay Seidel; Ewout R Brunt; Georg Auburger; Ludger Schöls; Katrin Bürk; Rob A I de Vos; W den Dunnen; I Bechmann; R Egensperger; Christine Van Broeckhoven; Kristin Gierga; Thomas Deller; Udo Rüb
Involvement of the auditory brainstem system in spinocerebellar ataxia type 2 (SCA2), type 3 (SCA3) and type 7 (SCA7).
Neuropathology and applied neurobiology 2008;34(5):479-91.
2007: Christine Zühlke; V Bernard; Andreas Dalski; P Lorenz; Beate Mitulla; Gabriele Gillessen-Kaesbach; Katrin Bürk
Screening of the SPTBN2 (SCA5) gene in German SCA patients.
Journal of neurology 2007;254(12):1649-52.
2007: Christine Zühlke; Katrin Bürk
Spinocerebellar ataxia type 17 is caused by mutations in the TATA-box binding protein.
Cerebellum (London, England) 2007;6(4):300-7.
2007: Katrin Bürk
Cognition in hereditary ataxia.
Cerebellum (London, England) 2007;6(3):280-6.
2006: christian beetz; Anders O H Nygren; Jörg Schickel; Michaela Auer-Grumbach; Katrin Bürk; G Heide; Jan Kassubek; Sven Klimpe; Thomas Klopstock; Friedmar R Kreuz; S Otto; Rebecca Schüle; Ludger Schöls; A-D Sperfeld; Otto W Witte; Thomas Deufel
High frequency of partial SPAST deletions in autosomal dominant hereditary spastic paraplegia.
Neurology 2006;67(11):1926-30.
2006: Matthias Reimold; Christoph Globas; Marc Gleichmann; Michael Schulze; Christian Gerloff; Roland Bares; Hans-Jürgen Machulla; Katrin Bürk
Spinocerebellar ataxia type 1, 2, and 3 and restless legs syndrome: striatal dopamine D2 receptor status investigated by [11C]raclopride positron emission tomography.
Movement disorders : official journal of the Movement Disorder Society 2006;21(10):1667-73.
2006: Peter Bauer; Friedmar R Kreuz; Katrin Bürk; Carsten Saft; Jürgen Andrich; Hubert Heilemann; Olaf Riess; Ludger Schöls
Mutations in TITF1 are not relevant to sporadic and familial chorea of unknown cause.
Movement disorders : official journal of the Movement Disorder Society 2006;21(10):1734-7.
2006: Andreas Dalski; Beate Mitulla; Katrin Bürk; Christoph Schattenfroh; Eberhard Schwinger; Christine Zühlke
Mutation of the highly conserved cysteine residue 131 of the SCA14 associated PRKCG gene in a family with slow progressive cerebellar ataxia.
Journal of neurology 2006;253(8):1111-2.
2006: Katrin Bürk; Irene Daum; Udo Rüb
Cognitive function in multiple system atrophy of the cerebellar type.
Movement disorders : official journal of the Movement Disorder Society 2006;21(6):772-6.
2006: Yoshio Ikeda; Katherine A Dick; Marcy R Weatherspoon; Dan Gincel; Karen R Armbrust; Joline C Dalton; Giovanni Stevanin; Alexandra Dürr; Christine Zühlke; Katrin Bürk; H Brent Clark; Alexis Brice; Jeffrey rothstein; Lawrence J Schut; John W Day; Laura P W Ranum
Spectrin mutations cause spinocerebellar ataxia type 5.
Nature genetics 2006;38(2):184-90.
2005: Udo Rüb; Kristin Gierga; Ewout R Brunt; Rob A I de Vos; M Bauer; Ludger Schöls; Katrin Bürk; Georg Auburger; Jürgen R E Bohl; Christian Schultz; Mario Vuksic; Guido J Burbach; Heiko Braak; Thomas Deller
Spinocerebellar ataxias types 2 and 3: degeneration of the pre-cerebellar nuclei isolates the three phylogenetically defined regions of the cerebellum.
Journal of neural transmission (Vienna, Austria : 1996) 2005;112(11):1523-45.
2005: Ullrich Wüllner; Matthias Reimold; Michael Abele; Katrin Bürk; Martina Minnerop; Bernd-Michael Dohmen; Hans-Jürgen Machulla; Roland Bares; Thomas Klockgether
Dopamine transporter positron emission tomography in spinocerebellar ataxias type 1, 2, 3, and 6.
Archives of neurology 2005;62(8):1280-5.
2005: Katrin Bürk; Udo Bühring; Jörg Bernhard Schulz; Christine Zühlke; Yorck Hellenbroich; Johannes Dichgans
Clinical and magnetic resonance imaging characteristics of sporadic cerebellar ataxia.
Archives of neurology 2005;62(6):981-5.
2005: Kristin Gierga; Katrin Bürk; M Bauer; G Orozco Diaz; Georg Auburger; Christian Schultz; Mario Vuksic; Ludger Schöls; Rob A I de Vos; Heiko Braak; Thomas Deller; Udo Rüb
Involvement of the cranial nerves and their nuclei in spinocerebellar ataxia type 2 (SCA2).
Acta neuropathologica 2005;109(6):617-31.
2005: Udo Rüb; Domenico Del Turco; Katrin Bürk; G Orozco Diaz; Georg Auburger; M Mittelbronn; Kristin Gierga; Estifanos Ghebremedhin; Christian Schultz; Ludger Schöls; Jürgen R E Bohl; Heiko Braak; Thomas Deller
Extended pathoanatomical studies point to a consistent affection of the thalamus in spinocerebellar ataxia type 2.
Neuropathology and applied neurobiology 2005;31(2):127-40.
2005: Katrin Bürk; Andreas Dalski; Sabine Purmann; Christine Zühlke
Detection of a novel SPG4-nonsense-mutation in a large German pedigree with pure spastic paraplegia.
Journal of neurology 2005;252(3):371.
2004: Christine Zühlke; A Budnik; Ulrike Gehlken; Andreas Dalski; Sabine Purmann; M Naumann; M Schmidt; Katrin Bürk; Eberhard Schwinger
FMR1 premutation as a rare cause of late onset ataxia--evidence for FXTAS in female carriers.
Journal of neurology 2004;251(11):1418-9.
2004: Udo Rüb; Katrin Bürk; Ludger Schöls; Ewout R Brunt; Rob A I de Vos; G Orozco Diaz; Kristin Gierga; Estifanos Ghebremedhin; Christian Schultz; Domenico Del Turco; M Mittelbronn; Georg Auburger; Thomas Deller; Heiko Braak
Damage to the reticulotegmental nucleus of the pons in spinocerebellar ataxia type 1, 2, and 3.
Neurology 2004;63(7):1258-63.
2004: Udo Rüb; Ewout R Brunt; Rob A I de Vos; Domenico Del Turco; Kelly Del Tredici; Kristin Gierga; Christian Schultz; Estifanos Ghebremedhin; Katrin Bürk; Georg Auburger; Heiko Braak
Degeneration of the central vestibular system in spinocerebellar ataxia type 3 (SCA3) patients and its possible clinical significance.
Neuropathology and applied neurobiology 2004;30(4):402-14.
2004: Yorck Hellenbroich; W Schulz-Schaeffer; Matthias F Nitschke; J Köhnke; G Händler; Katrin Bürk; Eberhard Schwinger; Christine Zühlke
Coincidence of a large SCA12 repeat allele with a case of Creutzfeld-Jacob disease.
Journal of neurology, neurosurgery, and psychiatry 2004;75(6):937-8.
2004: Matthias Habeck; Christine Zühlke; Karl H P Bentele; Stephan Unkelbach; Wolfram Kress; Katrin Bürk; Eberhard Schwinger; Yorck Hellenbroich
Aprataxin mutations are a rare cause of early onset ataxia in Germany.
Journal of neurology 2004;251(5):591-4.
2004: Katrin Bürk; Christine Zühlke; I R König; A Ziegler; Eberhard Schwinger; Christoph Globas; Johannes Dichgans; Yorck Hellenbroich
Spinocerebellar ataxia type 5: clinical and molecular genetic features of a German kindred.
Neurology 2004;62(2):327-9.
2003: Christoph Globas; S Bösch; Christine Zühlke; Irene Daum; Johannes Dichgans; Katrin Bürk
The cerebellum and cognition. Intellectual function in spinocerebellar ataxia type 6 (SCA6).
Journal of neurology 2003;250(12):1482-7.
2003: Ludger Schöls; Ingrid Bauer; Christine Zühlke; Thorsten Schulte; Christina Kölmel; Katrin Bürk; Helge Topka; Peter Bauer; Horst Przuntek; Olaf Riess
Do CTG expansions at the SCA8 locus cause ataxia?
Annals of neurology 2003;54(1):110-5.
2003: Heinz Wiendl; Matthias Mehling; J Dichgans; Arthur Melms; Katrin Bürk
The humoral response in the pathogenesis of gluten ataxia.
Neurology 2003;60(8):1397; author reply 1397-9.
2003: Katrin Bürk; Christoph Globas; S Bösch; Thomas Klockgether; Christine Zühlke; Irene Daum; Johannes Dichgans
Cognitive deficits in spinocerebellar ataxia type 1, 2, and 3.
Journal of neurology 2003;250(2):207-11.
2003: Christine Zühlke; Ulrike Gehlken; Yorck Hellenbroich; Eberhard Schwinger; Katrin Bürk
Phenotypical variability of expanded alleles in the TATA-binding protein gene. Reduced penetrance in SCA17?
Journal of neurology 2003;250(2):161-3.
2002: Michael Abele; Katrin Bürk; Ludger Schöls; S Schwartz; I Besenthal; Johannes Dichgans; Christine Zühlke; Olaf Riess; Thomas Klockgether
The aetiology of sporadic adult-onset ataxia.
Brain : a journal of neurology 2002;125(Pt 5):961-8.
2002: Christine Zühlke; Andreas Dalski; Yorck Hellenbroich; Stefanie Bubel; Eberhard Schwinger; Katrin Bürk
Spinocerebellar ataxia type 1 (SCA1): phenotype-genotype correlation studies in intermediate alleles.
European journal of human genetics : EJHG 2002;10(3):204-9.
2001: Katrin Bürk; Arthur Melms; J B Schulz; J Dichgans
Effectiveness of intravenous immunoglobin therapy in cerebellar ataxia associated with gluten sensitivity.
Annals of neurology 2001;50(6):827-8.
2001: Katrin Bürk; Martin Skalej; J Dichgans
High prevalence of CSF-containing cysts in superficial hemosiderosis of the central nervous system.
Journal of neurology 2001;248(11):1005-6.
2001: Katrin Bürk; Martin Skalej; Johannes Dichgans
Pontine MRI hyperintensities ("the cross sign") are not pathognomonic for multiple system atrophy (MSA).
Movement disorders : official journal of the Movement Disorder Society 2001;16(3):535.
2001: Katrin Bürk; S Bösch; Claudia A Müller; Arthur Melms; Christine Zühlke; M Stern; I Besenthal; Martin Skalej; P Ruck; S Ferber; Thomas Klockgether; Johannes Dichgans
Sporadic cerebellar ataxia associated with gluten sensitivity.
Brain : a journal of neurology 2001;124(Pt 5):1013-9.
2001: Michael Abele; Katrin Bürk; Franco Laccone; Johannes Dichgans; Thomas Klockgether
Restless legs syndrome in spinocerebellar ataxia types 1, 2, and 3.
Journal of neurology 2001;248(4):311-4.
2001: Katrin Bürk; S Bösch; Christoph Globas; Christine Zühlke; Irene Daum; Thomas Klockgether; Johannes Dichgans
Executive dysfunction in spinocerebellar ataxia type 1.
European neurology 2001;46(1):43-8.
2000: Jörg B Schulz; Thomas Dehmer; Ludger Schöls; H Mende; Cornelia Hardt; Matthias Vorgerd; Katrin Bürk; Wayne R Matson; Johannes Dichgans; M Flint Beal; Mikhail B Bogdanov
Oxidative stress in patients with Friedreich ataxia.
Neurology 2000;55(11):1719-21.
2000: Michael Abele; Jörg B Schulz; Katrin Bürk; Helge Topka; Johannes Dichgans; Thomas Klockgether
Evoked potentials in multiple system atrophy (MSA).
Acta neurologica Scandinavica 2000;101(2):111-5.
2000: Michael Abele; Jörg B Schulz; Katrin Bürk; Helge Topka; Johannes Dichgans; Thomas Klockgether
Nerve conduction studies in multiple system atrophy.
European neurology 2000;43(4):221-3.
1999: Andreas R Luft; Martin Skalej; Jörg B Schulz; D Welte; R Kolb; Katrin Bürk; Thomas Klockgether; K Voight
Patterns of age-related shrinkage in cerebellum and brainstem observed in vivo using three-dimensional MRI volumetry.
Cerebral cortex (New York, N.Y. : 1991) 1999;9(7):712-21.
1999: Katrin Bürk; Michael Fetter; Michael Abele; Franco Laccone; Alexis Brice; Johannes Dichgans; Thomas Klockgether
Autosomal dominant cerebellar ataxia type I: oculomotor abnormalities in families with SCA1, SCA2, and SCA3.
Journal of neurology 1999;246(9):789-97.
1999: Katrin Bürk; Thomas Klockgether; Johannes Dichgans
[New insights in the molecular genetics and pathophysiology of hereditary ataxias].
Der Nervenarzt 1999;70(6):491-5.
1999: O Didierjean; G Cancel; Giovanni Stevanin; Alexandra Dürr; Katrin Bürk; Ali Benomar; Agnes Lezin; Samir Belal; M Abada-Bendid; Thomas Klockgether; Alexis Brice
Linkage disequilibrium at the SCA2 locus.
Journal of medical genetics 1999;36(5):415-7.
1999: Katrin Bürk; Christoph Globas; S Bösch; Susanne Gräber; Michael Abele; Alexis Brice; Johannes Dichgans; Irene Daum; Thomas Klockgether
Cognitive deficits in spinocerebellar ataxia 2.
Brain : a journal of neurology 1999;122 ( Pt 4)():769-77.
1999: Michael Abele; Michael Weller; S Mescheriakov; Katrin Bürk; Johannes Dichgans; Thomas Klockgether
Cerebellar ataxia with glutamic acid decarboxylase autoantibodies.
Neurology 1999;52(4):857-9.
1999: Martin Dichgans; L Schöls; Jürgen Herzog; Giovanni Stevanin; H Weirich-Schwaiger; G Rouleau; Katrin Bürk; Thomas Klockgether; Christine Zühlke; Franco Laccone; Olaf Riess; Thomas Gasser
Spinocerebellar ataxia type 6: evidence for a strong founder effect among German families.
Neurology 1999;52(4):849-51.
1999: Thomas Klockgether; Ludger Schöls; Michael Abele; Katrin Bürk; Helge Topka; Frank Andres; Georgios Amoiridis; R Lüdtke; Olaf Riess; Franco Laccone; Johannes Dichgans
Age related axonal neuropathy in spinocerebellar ataxia type 3/Machado-Joseph disease (SCA3/MJD).
Journal of neurology, neurosurgery, and psychiatry 1999;66(2):222-4.
1998: Thomas Klockgether; Katrin Bürk; Ullrich Wüllner; Gregor Wenning; Jörg B Schulz; G Döller; Karl Wessel; P Huss; A Krämer; R Lüdtke
Risk factors for idiopathic cerebellar ataxia of late onset.
Journal of the neurological sciences 1998;160(2):171-4.
1998: Thomas Klockgether; Martin Skalej; D Wedekind; Andreas R Luft; D Welte; Jörg B Schulz; Michael Abele; Katrin Bürk; Franco Laccone; Alexis Brice; Johannes Dichgans
Autosomal dominant cerebellar ataxia type I. MRI-based volumetry of posterior fossa structures and basal ganglia in spinocerebellar ataxia types 1, 2 and 3.
Brain : a journal of neurology 1998;121 ( Pt 9)():1687-93.
1998: Andreas R Luft; Martin Skalej; D Welte; R Kolb; Katrin Bürk; Jörg B Schulz; Thomas Klockgether; K Voigt
A new semiautomated, three-dimensional technique allowing precise quantification of total and regional cerebellar volume using MRI.
Magnetic resonance in medicine : official journal of the Society of Magnetic Resonance in Medicine / Society of Magnetic Resonance in Medicine 1998;40(1):143-51.
1998: Thomas Klockgether; R Lüdtke; B Kramer; Michael Abele; Katrin Bürk; Ludger Schöls; Olaf Riess; Franco Laccone; Sylvia Boesch; I Lopes-Cendes; Alexis Brice; R Inzelberg; Nelly Zilber; Johannes Dichgans
The natural history of degenerative ataxia: a retrospective study in 466 patients.
Brain : a journal of neurology 1998;121 ( Pt 4)():589-600.
1997: Michael Abele; Katrin Bürk; Frank Andres; Helge Topka; Franco Laccone; S Bösch; Alexis Brice; G Cancel; Johannes Dichgans; Thomas Klockgether
Autosomal dominant cerebellar ataxia type I. Nerve conduction and evoked potential studies in families with SCA1, SCA2 and SCA3.
Brain : a journal of neurology 1997;120 ( Pt 12)():2141-8.
1997: Katrin Bürk; Michael Fetter; Martin Skalej; Franco Laccone; Giovanni Stevanin; Johannes Dichgans; Thomas Klockgether
Saccade velocity in idiopathic and autosomal dominant cerebellar ataxia.
Journal of neurology, neurosurgery, and psychiatry 1997;62(6):662-4.
1997: Olaf Riess; Franco Laccone; Suzana Gispert; Ludger Schöls; Christine Zühlke; AM Vieira-Saecker; S Herlt; Karl Wessel; Jörg T Epplen; Bernhard H F Weber; Friedmar R Kreuz; S Chahrokh-Zadeh; A Meindl; A Lunkes; J Aguiar; M Macek; A Krebsová; Milan Macek Jr.; Katrin Bürk; S Tinschert; I Schreyer; Stef pulst; Georg Auburger
SCA2 trinucleotide expansion in German SCA patients.
Neurogenetics 1997;1(1):59-64.
1997: G Cancel; Alexandra Dürr; O Didierjean; G Imbert; Katrin Bürk; Agnes Lezin; Samir Belal; Ali Benomar; M Abada-Bendib; C Vial; J Guimarães; H Chneiweiss; Giovanni Stevanin; Gaël Yvert; Nacer Abbas; Frédéric Saudou; Anne-Sophie Lebre; Mohamed Yahyaoui; Faycal Hentati; JC Vernant; Thomas Klockgether; Jean-Louis Mandel; Yves Agid; Alexis Brice
Molecular and clinical correlations in spinocerebellar ataxia 2: a study of 32 families.
Human molecular genetics 1997;6(5):709-15.
1997: Katrin Bürk; Giovanni Stevanin; O Didierjean; G Cancel; Yvon Trottier; Martin Skalej; Michael Abele; Alexis Brice; Johannes Dichgans; Thomas Klockgether
Clinical and genetic analysis of three German kindreds with autosomal dominant cerebellar ataxia type I linked to the SCA2 locus.
Journal of neurology 1997;244(4):256-61.
1996: Giovanni Stevanin; Yvon Trottier; G Cancel; Alexandra Dürr; G David; O Didierjean; Katrin Bürk; G Imbert; Frédéric Saudou; M Abada-Bendib; Isabelle Gourfinkel-An; Ali Benomar; Nacer Abbas; Thomas Klockgether; Djamel Grid; Yves Agid; Jean-Louis Mandel; Alexis Brice
Screening for proteins with polyglutamine expansions in autosomal dominant cerebellar ataxias.
Human molecular genetics 1996;5(12):1887-92.
1996: Katrin Bürk; Michael Abele; Michael Fetter; Johannes Dichgans; Martin Skalej; Franco Laccone; O Didierjean; Alexis Brice; Thomas Klockgether
Autosomal dominant cerebellar ataxia type I clinical features and MRI in families with SCA1, SCA2 and SCA3.
Brain : a journal of neurology 1996;119 ( Pt 5)():1497-505.
1996: Thomas Klockgether; Christine Zühlke; Jörg B Schulz; Katrin Bürk; Michael Fetter; Helmut Dittmann; Martin Skalej; Johannes Dichgans
Friedreich's ataxia with retained tendon reflexes: molecular genetics, clinical neurophysiology, and magnetic resonance imaging.
Neurology 1996;46(1):118-21.
1995: Thomas Klockgether; Katrin Bürk; Georg Auburger; J Dichgans
[Classification and diagnosis of degenerative ataxias].
Der Nervenarzt 1995;66(8):571-81.
1994: Thomas Klockgether; Katrin Bürk; Jörg B Schulz; J Dichgans; Karl Wessel; Georg Auburger
Absence of SCA1 mutation in idiopathic cerebellar ataxia.
Journal of neurology, neurosurgery, and psychiatry 1994;57(11):1439-40.