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...

The genetic background of Parkinson's disease: current progress and future prospects

Acta neurologica Scandinavica, 2016-11, Vol.134 (5), p.314-326

2016

Volltextzugriff (PDF)

Association of Genetic Polymorphisms in Kawasaki Disease with the Response to Intravenous Immunoglobulin Therapy

Pediatric cardiology, 2023, Vol.44 (1), p.1-12

2023

Volltextzugriff (PDF)

Pharmacological treatment and the prospect of pharmacogenetics in Parkinson's disease

International journal of clinical practice (Esher), 2011-12, Vol.65 (12), p.1289-1294

2011

Volltextzugriff (PDF)

Association of NFKB1, NKX2-5, GATA4 and RANKL gene polymorphisms with sporadic congenital heart disease in Greek patients

Balkan journal of medical genetics, 2021-07, Vol.24 (1), p.15-20

2021

Volltextzugriff (PDF)

A 2-year prospective densitometric study on the influence of Fok-I gene polymorphism in young patients with thalassaemia major

Osteoporosis international, 2016-02, Vol.27 (2), p.781-788

2016

Volltextzugriff (PDF)

Apelin and G212A apelin receptor gene polymorphism in obese and diabese youth

Pediatric obesity, 2015-06, Vol.10 (3), p.213-219

2015

Volltextzugriff (PDF)

The G2019S LRRK2 mutation is uncommon amongst Greek patients with sporadic Parkinson's disease

European journal of neurology, 2007-10, Vol.14 (10), p.1088-1090

2007

Volltextzugriff (PDF)

Pharmacogenetics and levodopa induced motor complications

International journal of neuroscience, 2019-04, Vol.129 (4), p.384-392

2019

Volltextzugriff (PDF)

No association of the Val158Met COMT polymorphism with Parkinson's disease in the Greek population

European journal of neurology, 2008-08, Vol.15 (8), p.e83-e83

2008

Volltextzugriff (PDF)

Association of phosphodiesterase 4D gene G0 haplotype and ischaemic stroke in a Greek population

European journal of neurology, 2007-07, Vol.14 (7), p.745-749

2007

Volltextzugriff (PDF)

PDXK mutations cause polyneuropathy responsive to pyridoxal 5′‐phosphate supplementation

Annals of neurology, 2019-08, Vol.86 (2), p.225-240

2019

Volltextzugriff (PDF)

Glutathion-S-Transferase P1 polymorphisms association with broncopulmonary dysplasia in preterm infants

Hippokratia, 2013-01, Vol.17 (4), p.363-367

2013

Volltextzugriff (PDF)

Identification of a mutation in the MTM1 gene, associated with X-linked myotubular myopathy, in a Greek family

Hippokratia, 2021-01, Vol.25 (2), p.99-99

2021

Volltextzugriff (PDF)

Identification of a mutation in the MTM1 gene, associated with X-linked myotubular myopathy, in a Greek family

Hippokratia, 2011-01, Vol.15 (3), p.278-279

2011

Volltextzugriff (PDF)

Identification of a novel mutation in the MTM1 gene associated with X-linked myotubular myopathy, in a Greek family

European journal of paediatric neurology, 2008, Vol.12, p.S53-S54

2008

Volltextzugriff (PDF)

P378Variant rs2200733 on chromosome 4q25 independently confers increased risk of atrial fibrillation in a greek population

Cardiovascular research, 2014-07, Vol.103 (suppl 1), p.S69-S69

2014

Volltextzugriff (PDF)

Pharmacological treatment and the prospect of pharmacogenetics in Parkinson’s disease: Pharmacogenetics and Parkinson‘s disease

International journal of clinical practice (Esher), 2011-12, Vol.65 (12), p.1289-1294

2011

Volltextzugriff (PDF)

Giant-Cell Tumor of the Rib in a 12-Year-Old Girl: A Case Report

Pediatric hematology and oncology, 2003, Vol.20 (4), p.351-355

2003

Volltextzugriff (PDF)

Lack of association between CX3CR1 V249I and T280M polymorphisms and risk of Parkinson's disease in a Greek population

Genetic testing and molecular biomarkers, 2012-08, Vol.16 (8), p.974-977

2012

Volltextzugriff (PDF)

Early-onset Alzheimer's disease caused by mutations at codon 717 of the β-amyloid precursor protein gene

Nature (London), 1991-10, Vol.353 (6347), p.844-846

1991

Volltextzugriff (PDF)

Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease

Nature (London), 1991-02, Vol.349 (6311), p.704-706

1991

Volltextzugriff (PDF)

An association study of a functional catalase gene polymorphism, −262C→T, and patients with Alzheimer's disease

Neuroscience letters, 2002-09, Vol.330 (2), p.210-212

2002

Volltextzugriff (PDF)

Cholesteryl ester transfer protein TaqI B and lipoprotein lipase Ser447Ter gene polymorphisms are not associated with ischaemic stroke in Greek patients

Neuroscience letters, 2005-08, Vol.384 (1), p.102-105

2005

Volltextzugriff (PDF)

An association study of the cholesteryl ester transfer protein TaqI B polymorphism with late onset Alzheimer's disease

Neuroscience letters, 2004-03, Vol.357 (2), p.152-154

2004

Volltextzugriff (PDF)

A locus for familial early-onset Alzheimer's disease on the long arm of chromosome 14, proximal to the alpha 1-antichymotrypsin gene

Nature genetics, 1992-12, Vol.2 (4), p.340-342

1992

Volltextzugriff (PDF)

1 – 25 von 81

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(72)
Mit Volltextzugriff
(65)

Publikationsform

Artikel
(80)
Berichte
(1)

Sprache

Englisch
(75)
Französisch
(6)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

The genetic background of Parkinson's disease: current progress and future prospects

Association of Genetic Polymorphisms in Kawasaki Disease with the Response to Intravenous Immunoglobulin Therapy

Pharmacological treatment and the prospect of pharmacogenetics in Parkinson's disease

Association of NFKB1, NKX2-5, GATA4 and RANKL gene polymorphisms with sporadic congenital heart disease in Greek patients

A 2-year prospective densitometric study on the influence of Fok-I gene polymorphism in young patients with thalassaemia major

Apelin and G212A apelin receptor gene polymorphism in obese and diabese youth

The G2019S LRRK2 mutation is uncommon amongst Greek patients with sporadic Parkinson's disease

Pharmacogenetics and levodopa induced motor complications

No association of the Val158Met COMT polymorphism with Parkinson's disease in the Greek population

Association of phosphodiesterase 4D gene G0 haplotype and ischaemic stroke in a Greek population

PDXK mutations cause polyneuropathy responsive to pyridoxal 5′‐phosphate supplementation

Glutathion-S-Transferase P1 polymorphisms association with broncopulmonary dysplasia in preterm infants

Identification of a mutation in the MTM1 gene, associated with X-linked myotubular myopathy, in a Greek family

Identification of a mutation in the MTM1 gene, associated with X-linked myotubular myopathy, in a Greek family

Identification of a novel mutation in the MTM1 gene associated with X-linked myotubular myopathy, in a Greek family

P378Variant rs2200733 on chromosome 4q25 independently confers increased risk of atrial fibrillation in a greek population

Pharmacological treatment and the prospect of pharmacogenetics in Parkinson’s disease: Pharmacogenetics and Parkinson‘s disease

Giant-Cell Tumor of the Rib in a 12-Year-Old Girl: A Case Report

Lack of association between CX3CR1 V249I and T280M polymorphisms and risk of Parkinson's disease in a Greek population

Early-onset Alzheimer's disease caused by mutations at codon 717 of the β-amyloid precursor protein gene

Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease

An association study of a functional catalase gene polymorphism, −262C→T, and patients with Alzheimer's disease

Cholesteryl ester transfer protein TaqI B and lipoprotein lipase Ser447Ter gene polymorphisms are not associated with ischaemic stroke in Greek patients

An association study of the cholesteryl ester transfer protein TaqI B polymorphism with late onset Alzheimer's disease

A locus for familial early-onset Alzheimer's disease on the long arm of chromosome 14, proximal to the alpha 1-antichymotrypsin gene

Suchergebnisse filtern