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Disgust in pre-clinical Huntington's disease: A longitudinal study

Neuropsychologia, 2006, Vol.44 (4), p.518-533

2006

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Mutations in ENPP1 are associated with 'idiopathic' infantile arterial calcification

Nature genetics, 2003-08, Vol.34 (4), p.379-381

2003

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Submicroscopic duplication in Xq28 causes increased expression of the MECP2 gene in a boy with severe mental retardation and features of Rett syndrome

Journal of medical genetics, 2005-02, Vol.42 (2), p.e12-e12

2005

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The Wegener’s granulomatosis quantitative trait locus on chromosome 6p21.3 as characterised by tagSNP genotyping

Annals of the rheumatic diseases, 2008-07, Vol.67 (7), p.972-979

2008

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Novel association of the CD226 (DNAM-1) Gly307Ser polymorphism in Wegener's granulomatosis and confirmation for multiple sclerosis in German patients

Genes and immunity, 2009-09, Vol.10 (6), p.591-595

2009

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Variation in the IL7RA and IL2RA genes in German multiple sclerosis patients

Journal of autoimmunity, 2009-03, Vol.32 (2), p.110-115

2009

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A novel form of autosomal recessive hereditary spastic paraplegia caused by a new SPG7 mutation

Neurology, 2007-07, Vol.69 (4), p.368-375

2007

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Mutations in the calcium-sensing receptor: A new genetic risk factor for chronic pancreatitis?

Scandinavian journal of gastroenterology, 2006-03, Vol.41 (3), p.343-348

2006

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Trinucleotide repeat expansion in SCA17/TBP in white patients with Huntington’s disease-like phenotype

Journal of medical genetics, 2004-03, Vol.41 (3), p.230-232

2004

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Autonomic nervous system function in Huntington's disease

Journal of neurology, neurosurgery and psychiatry, 2002-06, Vol.72 (6), p.726-731

2002

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Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn’s disease

Gut, 2005-10, Vol.54 (10), p.1421-1427

2005

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Familial parkinsonism with synuclein pathology: clinical and PET studies of A30P mutation carriers

Neurology, 2001-05, Vol.56 (10), p.1355-1362

2001

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Association of UCP2 −866 G A polymorphism with chronic inflammatory diseases

Genes and immunity, 2009-09, Vol.10 (6), p.601-605

2009

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Spinocerebellar ataxia type 6: genotype and phenotype in German kindreds

Journal of neurology, neurosurgery and psychiatry, 1998-01, Vol.64 (1), p.67-73

1998

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Increased Frequency of Migraine in Narcoleptic Patients: A Confirmatory Study

Cephalalgia, 2003-02, Vol.23 (1), p.14-19

2003

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Autosomal dominant cerebellar ataxia: Phenotypic differences in genetically defined subtypes?

Annals of neurology, 1997-12, Vol.42 (6), p.924-932

1997

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Early-onset ALS with long-term survival associated with spastin gene mutation

Neurology, 2005-07, Vol.65 (1), p.141-143

2005

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Analysis of variation in the IL7RA and IL2RA genes in atopic dermatitis

Journal of dermatological science, 2009-08, Vol.55 (2), p.138-140

2009

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A Polymorphism in the CD14 Gene is Associated with Crohn Disease

Scandinavian journal of gastroenterology, 2002, Vol.37 (2), p.189-191

2002

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Sex specifically associated promoter polymorphism in multiple sclerosis affects interleukin 4 expression levels

Genes and immunity, 2007-12, Vol.8 (8), p.703-706

2007

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Friedreich's ataxia: Revision of the phenotype according to molecular genetics

Brain (London, England : 1878), 1997-12, Vol.120 (12), p.2131-2140

1997

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Increased susceptibility to sporadic Parkinson's disease by a certain combined α-synuclein/apolipoprotein E genotype

Annals of neurology, 1999-05, Vol.45 (5), p.611-617

1999

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Apolipoprotein E genotypes do not influence the age of onset in Huntington’s disease

Journal of neurology, neurosurgery and psychiatry, 2004-12, Vol.75 (12), p.1692-1696

2004

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Unrelated queens coexist in colonies of the termite Macrotermes michaelseni

Molecular ecology, 2005-04, Vol.14 (5), p.1527-1532

2005

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Neurophysiological findings in SPG4 patients differ from other types of spastic paraplegia

Neurology, 2003-05, Vol.60 (9), p.1529-1532

2003

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Disgust in pre-clinical Huntington's disease: A longitudinal study

Mutations in ENPP1 are associated with 'idiopathic' infantile arterial calcification

Submicroscopic duplication in Xq28 causes increased expression of the MECP2 gene in a boy with severe mental retardation and features of Rett syndrome

The Wegener’s granulomatosis quantitative trait locus on chromosome 6p21.3 as characterised by tagSNP genotyping

Novel association of the CD226 (DNAM-1) Gly307Ser polymorphism in Wegener's granulomatosis and confirmation for multiple sclerosis in German patients

Variation in the IL7RA and IL2RA genes in German multiple sclerosis patients

A novel form of autosomal recessive hereditary spastic paraplegia caused by a new SPG7 mutation

Mutations in the calcium-sensing receptor: A new genetic risk factor for chronic pancreatitis?

Trinucleotide repeat expansion in SCA17/TBP in white patients with Huntington’s disease-like phenotype

Autonomic nervous system function in Huntington's disease

Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn’s disease

Familial parkinsonism with synuclein pathology: clinical and PET studies of A30P mutation carriers

Association of UCP2 −866 G A polymorphism with chronic inflammatory diseases

Spinocerebellar ataxia type 6: genotype and phenotype in German kindreds

Increased Frequency of Migraine in Narcoleptic Patients: A Confirmatory Study

Autosomal dominant cerebellar ataxia: Phenotypic differences in genetically defined subtypes?

Early-onset ALS with long-term survival associated with spastin gene mutation

Analysis of variation in the IL7RA and IL2RA genes in atopic dermatitis

A Polymorphism in the CD14 Gene is Associated with Crohn Disease

Sex specifically associated promoter polymorphism in multiple sclerosis affects interleukin 4 expression levels

Friedreich's ataxia: Revision of the phenotype according to molecular genetics

Increased susceptibility to sporadic Parkinson's disease by a certain combined α-synuclein/apolipoprotein E genotype

Apolipoprotein E genotypes do not influence the age of onset in Huntington’s disease

Unrelated queens coexist in colonies of the termite Macrotermes michaelseni

Neurophysiological findings in SPG4 patients differ from other types of spastic paraplegia

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