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ATXN8 −62 G/A promoter polymorphism and risk of Taiwanese Parkinson's disease

European journal of neurology, 2012-11, Vol.19 (11), p.1462-1469

2012

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Angiotensin-converting enzyme polymorphisms and risk of spontaneous deep intracranial hemorrhage in Taiwan

European journal of neurology, 2008-11, Vol.15 (11), p.1206-1211

2008

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Promoter polymorphisms modulating HSPA5 expression may increase susceptibility to Taiwanese Alzheimer’s disease

Journal of Neural Transmission, 2008-11, Vol.115 (11), p.1537-1543

2008

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Genetic testing in spinocerebellar ataxia in Taiwan: expansions of trinucleotide repeats in SCA8 and SCA17 are associated with typical Parkinson's disease

Clinical genetics, 2004-03, Vol.65 (3), p.209-214

2004

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Contribution of clinical screening to carrier detection in a large Chinese family with fabry disease due to a novel alpha-galactosidase A gene deletion

European journal of neurology, 2007-05, Vol.14 (5), p.493-497

2007

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Phenotypic variability in a Chinese family with rimmed vacuolar distal myopathy

Journal of neurology, neurosurgery and psychiatry, 2005-05, Vol.76 (5), p.752-755

2005

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Heat shock protein 70 and tumor necrosis factor alpha in Taiwanese patients with dementia

Dementia and geriatric cognitive disorders, 2005-01, Vol.20 (1), p.1-7

2005

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alpha-Synuclein promoter RsaI T-to-C polymorphism and the risk of Parkinson's disease

Journal of Neural Transmission, 2006-10, Vol.113 (10), p.1425-1433

2006

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Analysis of polyglutamine-coding repeats in the TATA-binding protein in different neurodegenerative diseases

Journal of Neural Transmission, 2005-04, Vol.112 (4), p.539-546

2005

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Mitochondrial DNA polymorphisms and the risk of Parkinson's disease in Taiwan

Journal of Neural Transmission, 2007-08, Vol.114 (8), p.1017-1021

2007

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Glucocerebrosidase gene mutation is a risk factor for early onset of Parkinson disease among Taiwanese

Journal of neurology, neurosurgery and psychiatry, 2007-09, Vol.78 (9), p.977-979

2007

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Mucopolysaccharidosis type I: Characterization of novel mutations affecting α- l-iduronidase activity

Clinical genetics, 1999-07, Vol.56 (1), p.66-70

1999

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DNA Haplotype Analysis of CAG Repeat in Taiwanese Huntington’s Disease Patients

European neurology, 2004-01, Vol.52 (2), p.96-100

2004

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Identification and characterization of mutations underlying Sanfilippo syndrome type A (mucopolysaccharidosis type IIIA)

Clinical genetics, 2002-03, Vol.61 (3), p.192-197

2002

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Identification and haplotype analysis of apolipoprotein B-100 Arg3500->Trp mutation in hyperlipidemic Chinese

Clinical chemistry (Baltimore, Md.), 1998-08, Vol.44 (8), p.1659-1665

1998

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Analysis of the UCHL1 genetic variant in Parkinson's disease among Chinese

Neurobiology of aging, 2010-12, Vol.31 (12), p.2194-2196

2010

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Analysis of heat-shock protein 70 gene polymorphisms and the risk of Parkinson's disease

Human genetics, 2004-02, Vol.114 (3), p.236-241

2004

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Identification and characterisation of mutations underlying Sanfilippo syndrome type B (mucopolysaccharidosis type IIIB)

Journal of medical genetics, 2002-02, Vol.39 (2), p.e3-3

2002

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Apolipoprotein E, angiotensin-converting enzyme and kallikrein gene polymorphisms and the risk of Alzheimer's disease and vascular dementia

Journal of Neural Transmission, 2006-10, Vol.113 (10), p.1499-1509

2006

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Identification and characterization of -3c-g acceptor splice site mutation in human α- l-iduronidase associated with mucopolysaccharidosis type IH/S

Clinical genetics, 2000-02, Vol.57 (2), p.131-136

2000

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Interleukin-1 alpha polymorphism has influence on late-onset sporadic Parkinson's disease in Taiwan

Journal of Neural Transmission, 2007-09, Vol.114 (9), p.1173-1177

2007

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Expression studies of mutations underlying Taiwanese Hunter syndrome (mucopolysaccharidosis type II)

Human genetics, 2005-02, Vol.116 (3), p.160-166

2005

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Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease

The New England journal of medicine, 2009-10, Vol.361 (17), p.1651-1661

2009

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Evolutionarily selected replication origins: functional aspects and structural organization

Molecular and Cellular Biology, 1986-09, Vol.6 (9), p.3077-3085

1986

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Correlation of HER-2/neu Amplification With Expression and With Other Prognostic Factors in 1103 Breast Cancers

JNCI : Journal of the National Cancer Institute, 1992-08, Vol.84 (16), p.1279-1282

1992

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ATXN8 −62 G/A promoter polymorphism and risk of Taiwanese Parkinson's disease

Angiotensin-converting enzyme polymorphisms and risk of spontaneous deep intracranial hemorrhage in Taiwan

Promoter polymorphisms modulating HSPA5 expression may increase susceptibility to Taiwanese Alzheimer’s disease

Genetic testing in spinocerebellar ataxia in Taiwan: expansions of trinucleotide repeats in SCA8 and SCA17 are associated with typical Parkinson's disease

Contribution of clinical screening to carrier detection in a large Chinese family with fabry disease due to a novel alpha-galactosidase A gene deletion

Phenotypic variability in a Chinese family with rimmed vacuolar distal myopathy

Heat shock protein 70 and tumor necrosis factor alpha in Taiwanese patients with dementia

alpha-Synuclein promoter RsaI T-to-C polymorphism and the risk of Parkinson's disease

Analysis of polyglutamine-coding repeats in the TATA-binding protein in different neurodegenerative diseases

Mitochondrial DNA polymorphisms and the risk of Parkinson's disease in Taiwan

Glucocerebrosidase gene mutation is a risk factor for early onset of Parkinson disease among Taiwanese

Mucopolysaccharidosis type I: Characterization of novel mutations affecting α- l-iduronidase activity

DNA Haplotype Analysis of CAG Repeat in Taiwanese Huntington’s Disease Patients

Identification and characterization of mutations underlying Sanfilippo syndrome type A (mucopolysaccharidosis type IIIA)

Identification and haplotype analysis of apolipoprotein B-100 Arg3500->Trp mutation in hyperlipidemic Chinese

Analysis of the UCHL1 genetic variant in Parkinson's disease among Chinese

Analysis of heat-shock protein 70 gene polymorphisms and the risk of Parkinson's disease

Identification and characterisation of mutations underlying Sanfilippo syndrome type B (mucopolysaccharidosis type IIIB)

Apolipoprotein E, angiotensin-converting enzyme and kallikrein gene polymorphisms and the risk of Alzheimer's disease and vascular dementia

Identification and characterization of -3c-g acceptor splice site mutation in human α- l-iduronidase associated with mucopolysaccharidosis type IH/S

Interleukin-1 alpha polymorphism has influence on late-onset sporadic Parkinson's disease in Taiwan

Expression studies of mutations underlying Taiwanese Hunter syndrome (mucopolysaccharidosis type II)

Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease

Evolutionarily selected replication origins: functional aspects and structural organization

Correlation of HER-2/neu Amplification With Expression and With Other Prognostic Factors in 1103 Breast Cancers

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