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Sporadic cerebellar ataxia associated with gluten sensitivity

Brain (London, England : 1878), 2001-05, Vol.124 (5), p.1013-1019

2001

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MRI‐based volumetric differentiation of sporadic cerebellar ataxia

Brain (London, England : 1878), 2004-01, Vol.127 (1), p.175-181

2004

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Spinocerebellar ataxia type 4 (SCA4): Initial pathoanatomical study reveals widespread cerebellar and brainstem degeneration

Journal of Neural Transmission, 2006-07, Vol.113 (7), p.829-843

2006

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DNA analysis of Huntington's disease: five years of experience in Germany, Austria, and Switzerland

Neurology, 1999-09, Vol.53 (4), p.801-801

1999

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The aetiology of sporadic adult-onset ataxia

Brain (London, England : 1878), 2002-05, Vol.125 (5), p.961-968

2002

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Executive Dysfunction in Spinocerebellar Ataxia Type 1

European neurology, 2001-01, Vol.46 (1), p.43-48

2001

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The GAA repeat expansion in intron 1 of the frataxin gene is related to the severity of cardiac manifestation in patients with Friedreich's ataxia

Journal of molecular medicine (Berlin, Germany), 2001, Vol.78 (11), p.626-632

2001

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Spectrin mutations cause spinocerebellar ataxia type 5

Nature genetics, 2006-02, Vol.38 (2), p.184-190

2006

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Expansion of the (CAG)n repeat causing Huntington's disease in 352 patients of German origin

Human molecular genetics, 1993-09, Vol.2 (9), p.1467-1469

1993

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SCA2 trinucleotide expansion in German SCA patients

Neurogenetics, 1997-05, Vol.1 (1), p.59-64

1997

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FMR1 premutation as a rare cause of late onset ataxia--evidence for FXTAS in female carriers

Journal of neurology, 2004-11, Vol.251 (11), p.1418-1419

2004

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The cerebellum and cognition: Intellectual function in spinocerebellar ataxia type 6 (SCA6)

Journal of neurology, 2003-12, Vol.250 (12), p.1482-1487

2003

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Do CTG expansions at the SCA8 locus cause ataxia?

Annals of neurology, 2003-07, Vol.54 (1), p.110-115

2003

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Premutations in the FMR1 gene as a modifying factor in Parkin-associated Parkinson's disease?

Movement disorders, 2005-08, Vol.20 (8), p.1060-1062

2005

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Phenotypical variability of expanded alleles in the TATA-binding protein gene: Reduced penetrance in SCA17?

Journal of neurology, 2003-02, Vol.250 (2), p.161-163

2003

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R124C mutation of the betaIGH3 gene leads to remarkable phenotypic variability in a Greek four-generation family with lattice corneal dystrophy type 1

Ophthalmologica (Basel), 2001-11, Vol.215 (6), p.444-447

2001

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Spinocerebellar ataxia type 1 (SCA1): phenotype-genotype correlation studies in intermediate alleles

European journal of human genetics : EJHG, 2002-03, Vol.10 (3), p.204-209

2002

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Conversion of recent-onset atrial fibrillation or flutter with ibutilide after amiodarone has failed

Intensive care medicine, 2002-07, Vol.28 (7), p.925-929

2002

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SCA6 is caused by moderate CAG expansion in the alpha1A-voltage-dependent calcium channel gene

Human molecular genetics, 1997-08, Vol.6 (8), p.1289-1293

1997

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Clinical and magnetic resonance imaging characteristics of sporadic cerebellar ataxia

Archives of neurology (Chicago), 2005-06, Vol.62 (6), p.981

2005

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Lung fibroblasts from patients with emphysema show a reduced proliferation rate in culture

The European respiratory journal, 2004-10, Vol.24 (4), p.575-579

2004

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Molecular Characterization of BCL6 Breakpoints in Primary Diffuse Large B-cell Lymphomas of the Central Nervous System Identifies GAPD as Novel Translocation Partner

Brain pathology (Zurich, Switzerland), 2003-10, Vol.13 (4), p.534-538

2003

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Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21

Human genetics, 2016-08, Vol.135 (8), p.923-938

2016

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Interphase Cytogenetic Analysis of Lymphoma-Associated Chromosomal Breakpoints in Primary Diffuse Large B-Cell Lymphomas of the Central Nervous System

Journal of neuropathology and experimental neurology, 2002-10, Vol.61 (10), p.926-933

2002

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Prevalence of the HOXB13 G84E prostate cancer risk allele in men treated with radical prostatectomy

BJU international, 2014-05, Vol.113 (5), p.830-835

2014

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Sporadic cerebellar ataxia associated with gluten sensitivity

MRI‐based volumetric differentiation of sporadic cerebellar ataxia

Spinocerebellar ataxia type 4 (SCA4): Initial pathoanatomical study reveals widespread cerebellar and brainstem degeneration

DNA analysis of Huntington's disease: five years of experience in Germany, Austria, and Switzerland

The aetiology of sporadic adult-onset ataxia

Executive Dysfunction in Spinocerebellar Ataxia Type 1

The GAA repeat expansion in intron 1 of the frataxin gene is related to the severity of cardiac manifestation in patients with Friedreich's ataxia

Spectrin mutations cause spinocerebellar ataxia type 5

Expansion of the (CAG)n repeat causing Huntington's disease in 352 patients of German origin

SCA2 trinucleotide expansion in German SCA patients

FMR1 premutation as a rare cause of late onset ataxia--evidence for FXTAS in female carriers

The cerebellum and cognition: Intellectual function in spinocerebellar ataxia type 6 (SCA6)

Do CTG expansions at the SCA8 locus cause ataxia?

Premutations in the FMR1 gene as a modifying factor in Parkin-associated Parkinson's disease?

Phenotypical variability of expanded alleles in the TATA-binding protein gene: Reduced penetrance in SCA17?

R124C mutation of the betaIGH3 gene leads to remarkable phenotypic variability in a Greek four-generation family with lattice corneal dystrophy type 1

Spinocerebellar ataxia type 1 (SCA1): phenotype-genotype correlation studies in intermediate alleles

Conversion of recent-onset atrial fibrillation or flutter with ibutilide after amiodarone has failed

SCA6 is caused by moderate CAG expansion in the alpha1A-voltage-dependent calcium channel gene

Clinical and magnetic resonance imaging characteristics of sporadic cerebellar ataxia

Lung fibroblasts from patients with emphysema show a reduced proliferation rate in culture

Molecular Characterization of BCL6 Breakpoints in Primary Diffuse Large B-cell Lymphomas of the Central Nervous System Identifies GAPD as Novel Translocation Partner

Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21

Interphase Cytogenetic Analysis of Lymphoma-Associated Chromosomal Breakpoints in Primary Diffuse Large B-Cell Lymphomas of the Central Nervous System

Prevalence of the HOXB13 G84E prostate cancer risk allele in men treated with radical prostatectomy

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