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Secondary pool boiling effects

Applied physics letters, 2016-02, Vol.108 (5)

2016

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Cognitive deficits in spinocerebellar ataxia type 1, 2, and 3

Journal of neurology, 2003-02, Vol.250 (2), p.207-211

2003

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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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Spinocerebellar ataxia type 5: clinical and molecular genetic features of a German kindred

Neurology, 2004-01, Vol.62 (2), p.327

2004

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Unraveling the formation dynamics of metallic femtosecond laser induced periodic surface structures

Optics and laser technology, 2024-04, Vol.171, p.110410, Article 110410

2024

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Different types of repeat expansion in the TATA-binding protein gene are associated with a new form of inherited ataxia

European journal of human genetics : EJHG, 2001-03, Vol.9 (3), p.160-164

2001

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Refinement of the spinocerebellar ataxia type 4 locus in a large German family and exclusion of CAG repeat expansions in this region

Journal of neurology, 2003-06, Vol.250 (6), p.668-671

2003

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Spinocerebellar ataxia type 4 : Investigation of 34 candidate genes

Journal of neurology, 2005-12, Vol.252 (12), p.1472-1475

2005

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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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Sporadic cerebellar ataxia associated with gluten sensitivity

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

2001

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Coincidence of a large SCA12 repeat allele with a case of Creutzfeld-Jacob disease

Journal of neurology, neurosurgery and psychiatry, 2004-06, Vol.75 (6), p.937-938

2004

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Friedreich's ataxia with retained tendon reflexes: molecular genetics, clinical neurophysiology, and magnetic resonance imaging

Neurology, 1996-01, Vol.46 (1), p.118

1996

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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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Machado-Joseph disease presenting as severe generalised dystonia in a German patient

Journal of neurology, 1999-09, Vol.246 (9), p.840-842

1999

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Morphological basis for the spectrum of clinical deficits in spinocerebellar ataxia 17 (SCA17)

Brain (London, England : 1878), 2006-09, Vol.129 (9), p.2341-2352

2006

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Focal dystonia as a presenting sign of spinocerebellar ataxia 17

Movement disorders, 2004-02, Vol.19 (2), p.217-220

2004

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Extension of the mutation spectrum in Friedreich's ataxia: detection of an exon deletion and novel missense mutations

European journal of human genetics : EJHG, 2004-11, Vol.12 (11), p.979-982

2004

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SCA17 caused by homozygous repeat expansion in TBP due to partial isodisomy 6

European journal of human genetics : EJHG, 2003-08, Vol.11 (8), p.629-632

2003

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Genomic organization of the human NFAT5 gene: exon-intron structure of the 14-kb transcript and CpG-island analysis of the promoter region

Cytogenetics and cell genetics, 2001-01, Vol.93 (3-4), p.239

2001

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Predominant dystonia with marked cerebellar atrophy: a rare phenotype in familial dystonia

Neurology, 2007-06, Vol.68 (24), p.2157; author reply 2157

2007

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Study of secondary pool boiling effects with functionalized surfaces created via Femtosecond Laser Surface Processing

2016 15th IEEE Intersociety Conference on Thermal and Thermomechanical Phenomena in Electronic Systems (ITherm), 2016, p.352-358

2016

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Spinocerebellar ataxia type 7: frequency of CAG repeat length in a German family

Journal of neurology, 1999-11, Vol.246 (11), p.1105-1106

1999

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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

1999

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Spinocerebellar ataxia type 4 and 16q22.1-linked Japanese ataxia are not allelic

Journal of neurology, 2008-04, Vol.255 (4), p.612-613

2008

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Mutation analysis in the fibroblast growth factor 14 gene: frameshift mutation and polymorphisms in patients with inherited ataxias

European journal of human genetics : EJHG, 2005-01, Vol.13 (1), p.118-120

2005

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Secondary pool boiling effects

Cognitive deficits in spinocerebellar ataxia type 1, 2, and 3

The aetiology of sporadic adult-onset ataxia

Spinocerebellar ataxia type 5: clinical and molecular genetic features of a German kindred

Unraveling the formation dynamics of metallic femtosecond laser induced periodic surface structures

Different types of repeat expansion in the TATA-binding protein gene are associated with a new form of inherited ataxia

Refinement of the spinocerebellar ataxia type 4 locus in a large German family and exclusion of CAG repeat expansions in this region

Spinocerebellar ataxia type 4 : Investigation of 34 candidate genes

Spectrin mutations cause spinocerebellar ataxia type 5

Sporadic cerebellar ataxia associated with gluten sensitivity

Coincidence of a large SCA12 repeat allele with a case of Creutzfeld-Jacob disease

Friedreich's ataxia with retained tendon reflexes: molecular genetics, clinical neurophysiology, and magnetic resonance imaging

MRI‐based volumetric differentiation of sporadic cerebellar ataxia

Machado-Joseph disease presenting as severe generalised dystonia in a German patient

Morphological basis for the spectrum of clinical deficits in spinocerebellar ataxia 17 (SCA17)

Focal dystonia as a presenting sign of spinocerebellar ataxia 17

Extension of the mutation spectrum in Friedreich's ataxia: detection of an exon deletion and novel missense mutations

SCA17 caused by homozygous repeat expansion in TBP due to partial isodisomy 6

Genomic organization of the human NFAT5 gene: exon-intron structure of the 14-kb transcript and CpG-island analysis of the promoter region

Predominant dystonia with marked cerebellar atrophy: a rare phenotype in familial dystonia

Study of secondary pool boiling effects with functionalized surfaces created via Femtosecond Laser Surface Processing

Spinocerebellar ataxia type 7: frequency of CAG repeat length in a German family

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

Spinocerebellar ataxia type 4 and 16q22.1-linked Japanese ataxia are not allelic

Mutation analysis in the fibroblast growth factor 14 gene: frameshift mutation and polymorphisms in patients with inherited ataxias

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