UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Contribution of glucocerebrosidase mutation in a large cohort of sporadic Parkinson's disease in Taiwan

European journal of neurology, 2011-10, Vol.18 (10), p.1227-1232

2011

Volltextzugriff (PDF)

A longitudinal study of Taiwanese Sialidosis type 1: an insight into the concept of cherry-red spot myoclonus syndrome

European journal of neurology, 2009-08, Vol.16 (8), p.912-919

2009

Volltextzugriff (PDF)

PARK6-linked autosomal recessive early-onset parkinsonism in Asian populations

Neurology, 2004-10, Vol.63 (8), p.1482-1485

2004

Volltextzugriff (PDF)

Analysis of candidate genes on chromosome 2 in oral cleft case-parent trios from three populations

Human genetics, 2006-11, Vol.120 (4), p.501-518

2006

Volltextzugriff (PDF)

LRRK2 MUTATION ANALYSIS IN PARKINSON DISEASE FAMILIES WITH EVIDENCE OF LINKAGE TO PARK8

Neurology, 2008-06, Vol.70 (24), p.2348-2349

2008

Volltextzugriff (PDF)

Nuclear β-catenin expression is closely related to ulcerative growth of colorectal carcinoma

British journal of cancer, 2002-04, Vol.86 (7), p.1124-1129

2002

Volltextzugriff (PDF)

Clinical and genetic studies on familial parkinsonism: The first report on a parkin gene mutation in a Taiwanese family

Movement disorders, 2001-01, Vol.16 (1), p.164-166

2001

Volltextzugriff (PDF)

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

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

2010

Volltextzugriff (PDF)

LRRK2 G2385R modulates age at onset in Parkinson's disease: A multi-center pooled analysis

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2009-10, Vol.150B (7), p.1022-1023

2009

Volltextzugriff (PDF)

Association study between candidate genes involved in cell-cell adhesion and non-syndromic cleft lip with or without cleft palate in Chinese population

Beijing da xue xue bao. Journal of Peking University. Yi xue ban, 2016-06, Vol.48 (3), p.403

2016

Volltextzugriff (PDF)

Genetic and DAT imaging studies of familial parkinsonism in a Taiwanese cohort

Journal of neural transmission. Supplementum, 2006 (70), p.235-240

2006

Volltextzugriff (PDF)

P1.062 Genetic contribution to young onset dystonia in a Taiwanese cohort

Parkinsonism & related disorders, 2009, Vol.15, p.S44-S45

2009

Volltextzugriff (PDF)

P3.153 PLA2G6 mutations in a Taiwanese cohort of early onset parkinsonism

Parkinsonism & related disorders, 2009, Vol.15, p.S187-S187

2009

Volltextzugriff (PDF)

A comprehensive analysis of the association of common variants of ABCG2 with gout

Scientific reports, 2017-08, Vol.7 (1), p.9988-8, Article 9988

2017

Volltextzugriff (PDF)

HLA-DRB1 antigens in Taiwanese patients with juvenile-onset systemic lupus erythematosus

Rheumatology international, 2001-11, Vol.21 (3), p.103-105

2001

Volltextzugriff (PDF)

The LRRK2 I2012T, G2019S, and I2020T mutations are rare in Taiwanese patients with sporadic Parkinson's disease

Parkinsonism & related disorders, 2005-12, Vol.11 (8), p.521-522

2005

Volltextzugriff (PDF)

Re: LRRK2 mutation analysis in Parkinson disease families with evidence of linkage to PARK8

Neurology, 2008-06, Vol.70 (24), p.2348; author reply 2348

2008

Volltextzugriff (PDF)

Nuclear [beta]-catenin expression is closely related to ulcerative growth of colorectal carcinoma

British journal of cancer, 2002-04, Vol.86 (7), p.1124

2002

Volltextzugriff (PDF)

Frequent allelic loss on chromosomes 4q and 16q associated with human hepatocellular carcinoma in Taiwan

Cancer letters, 1998-01, Vol.123 (1), p.1-6

1998

Volltextzugriff (PDF)

p16INK4 gene mutation and allelic loss of chromosome 9p21-22 in Taiwanese hepatocellular carcinoma

Anticancer research, 2000-05, Vol.20 (3A), p.1621

2000

Volltextzugriff (PDF)

Pembrolizumab as Second-Line Therapy for Advanced Urothelial Carcinoma

The New England journal of medicine, 2017-03, Vol.376 (11), p.1015-1026

2017

Volltextzugriff (PDF)

Overcoming Radiation Resistance by Iron-Platinum Metal Alloy Nanoparticles in Human Copper Transport 1-Overexpressing Cancer Cells via Mitochondrial Disturbance

International journal of nanomedicine, 2021-01, Vol.16, p.2071-2085

2021

Volltextzugriff (PDF)

Acupuncture Treatment Reduced the Risk of Coronary Heart Disease in Patients with Depression: A Propensity-Score Matched Cohort Study

Neuropsychiatric disease and treatment, 2021-01, Vol.17, p.2315-2325

2021

Volltextzugriff (PDF)

Prognostic Significance of Co-expression of RON and MET Receptors in Node-Negative Breast Cancer Patients

Clinical cancer research, 2005-03, Vol.11 (6), p.2222-2228

2005

Volltextzugriff (PDF)

1 – 25 von 96

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(93)
Mit Volltextzugriff
(83)

Publikationsform

Artikel
(96)

Sprache

Englisch
(94)
Chinesisch
(2)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Contribution of glucocerebrosidase mutation in a large cohort of sporadic Parkinson's disease in Taiwan

A longitudinal study of Taiwanese Sialidosis type 1: an insight into the concept of cherry-red spot myoclonus syndrome

PARK6-linked autosomal recessive early-onset parkinsonism in Asian populations

Analysis of candidate genes on chromosome 2 in oral cleft case-parent trios from three populations

LRRK2 MUTATION ANALYSIS IN PARKINSON DISEASE FAMILIES WITH EVIDENCE OF LINKAGE TO PARK8

Nuclear β-catenin expression is closely related to ulcerative growth of colorectal carcinoma

Clinical and genetic studies on familial parkinsonism: The first report on a parkin gene mutation in a Taiwanese family

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

LRRK2 G2385R modulates age at onset in Parkinson's disease: A multi-center pooled analysis

Association study between candidate genes involved in cell-cell adhesion and non-syndromic cleft lip with or without cleft palate in Chinese population

Phenotype, genotype, and worldwide genetic penetrance of LRRK2 -associated Parkinson's disease: a case-control study

Genetic and DAT imaging studies of familial parkinsonism in a Taiwanese cohort

P1.062 Genetic contribution to young onset dystonia in a Taiwanese cohort

P3.153 PLA2G6 mutations in a Taiwanese cohort of early onset parkinsonism

A comprehensive analysis of the association of common variants of ABCG2 with gout

HLA-DRB1 antigens in Taiwanese patients with juvenile-onset systemic lupus erythematosus

The LRRK2 I2012T, G2019S, and I2020T mutations are rare in Taiwanese patients with sporadic Parkinson's disease

Re: LRRK2 mutation analysis in Parkinson disease families with evidence of linkage to PARK8

Nuclear [beta]-catenin expression is closely related to ulcerative growth of colorectal carcinoma

Frequent allelic loss on chromosomes 4q and 16q associated with human hepatocellular carcinoma in Taiwan

p16INK4 gene mutation and allelic loss of chromosome 9p21-22 in Taiwanese hepatocellular carcinoma

Pembrolizumab as Second-Line Therapy for Advanced Urothelial Carcinoma

Overcoming Radiation Resistance by Iron-Platinum Metal Alloy Nanoparticles in Human Copper Transport 1-Overexpressing Cancer Cells via Mitochondrial Disturbance

Acupuncture Treatment Reduced the Risk of Coronary Heart Disease in Patients with Depression: A Propensity-Score Matched Cohort Study

Prognostic Significance of Co-expression of RON and MET Receptors in Node-Negative Breast Cancer Patients

Suchergebnisse filtern