UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 55

Sortiert nach

High-Sensitivity CRP Discriminates HNF1A-MODY From Other Subtypes of Diabetes

Diabetes care, 2011-08, Vol.34 (8), p.1860-1862

2011

Link zum Volltext

Verfügbarkeit prüfen

Assessment of High-Sensitivity C-Reactive Protein Levels as Diagnostic Discriminator of Maturity-Onset Diabetes of the Young Due to HNF1A Mutations

Diabetes care, 2010-09, Vol.33 (9), p.1919-1924

2010

Link zum Volltext

Verfügbarkeit prüfen

Large-Scale Association Studies of Variants in Genes Encoding the Pancreatic β-Cell KATP Channel Subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) Confirm That the KCNJ11 E23K Variant Is Associated With Type 2 Diabetes

Diabetes (New York, N.Y.), 2003-02, Vol.52 (2), p.568-572

2003

Link zum Volltext

Verfügbarkeit prüfen

Diagnosis and management of maturity onset diabetes of the young (MODY)

BMJ (Online), 2011-10, Vol.343 (7828), p.d6044

International edition, 2011

Link zum Volltext

Verfügbarkeit prüfen

Lixisenatide in type 1 diabetes: A randomised control trial of the effect of lixisenatide on post‐meal glucose excursions and glucagon in type 1 diabetes patients

Endocrinology, diabetes & metabolism, 2020-07, Vol.3 (3), p.e00130-n/a

2020

Link zum Volltext

Verfügbarkeit prüfen

Evaluation of Serum 1,5 Anhydroglucitol Levels as a Clinical Test to Differentiate Subtypes of Diabetes

Diabetes care, 2010-02, Vol.33 (2), p.252-257

2010

Link zum Volltext

Verfügbarkeit prüfen

Transdermal Blood Sampling for C-Peptide Is a Minimally Invasive, Reliable Alternative to Venous Sampling in Children and Adults With Type 1 Diabetes

Diabetes care, 2024-02, Vol.47 (2), p.239

2024

Link zum Volltext

Verfügbarkeit prüfen

Monogenic diabetes: old and new approaches to diagnosis

Clinical medicine (London, England), 2013-06, Vol.13 (3), p.278-281

Owen, Katharine R

2013

Link zum Volltext

Verfügbarkeit prüfen

281-OR: Type 2 Diabetes Diagnosed between 16-30 Years in South Asian and White Individuals Is Phenotypically Similar

Diabetes (New York, N.Y.), 2020-06, Vol.69 (Supplement_1)

2020

Link zum Volltext

Verfügbarkeit prüfen

Plasma Fucosylated Glycans and C-Reactive Protein as Biomarkers of HNF1A-MODY in Young Adult-Onset Nonautoimmune Diabetes

Diabetes care, 2019-01, Vol.42 (1), p.17-26

2019

Link zum Volltext

Verfügbarkeit prüfen

Common Variant in the FTO Gene Is Associated with Body Mass Index and Predisposes to Childhood and Adult Obesity

Science (American Association for the Advancement of Science), 2007-05, Vol.316 (5826), p.889-894

2007

Link zum Volltext

Verfügbarkeit prüfen

Replication of Genome-Wide Association Signals in UK Samples Reveals Risk Loci for Type 2 Diabetes

Science (American Association for the Advancement of Science), 2007-06, Vol.316 (5829), p.1336-1341

2007

Link zum Volltext

Verfügbarkeit prüfen

Common Variants of the Hepatocyte Nuclear Factor-4α P2 Promoter Are Associated With Type 2 Diabetes in the U.K. Population

Diabetes (New York, N.Y.), 2004-11, Vol.53 (11), p.3002-3006

2004

Link zum Volltext

Verfügbarkeit prüfen

Interlaboratory evaluation of plasma N-glycan antennary fucosylation as a clinical biomarker for HNF1A-MODY using liquid chromatography methods

Glycoconjugate journal, 2021-06, Vol.38 (3), p.375-386

2021

Link zum Volltext

Verfügbarkeit prüfen

The Variable Number of Tandem Repeats Upstream of the Insulin Gene Is a Susceptibility Locus for Latent Autoimmune Diabetes in Adults

Diabetes (New York, N.Y.), 2006-06, Vol.55 (6), p.1890-1894

2006

Link zum Volltext

Verfügbarkeit prüfen

A Large-Scale Association Analysis of Common Variation of the HNF1α Gene With Type 2 Diabetes in the U.K. Caucasian Population

Diabetes (New York, N.Y.), 2005-08, Vol.54 (8), p.2487-2491

2005

Link zum Volltext

Verfügbarkeit prüfen

Altered cortisol metabolism in individuals with HNF1A‐MODY

Clinical endocrinology (Oxford), 2020-09, Vol.93 (3), p.269-279

2020

Link zum Volltext

Verfügbarkeit prüfen

1900-P: HNF1A Deficiency Leads to Perturbed Glucagon Secretion in Humans

Diabetes (New York, N.Y.), 2020-06, Vol.69 (Supplement_1)

2020

Link zum Volltext

Verfügbarkeit prüfen

PAX6 mutation in association with ptosis, cataract, iris hypoplasia, corneal opacification and diabetes: a new variant of familial aniridia?

Clinical & experimental ophthalmology, 2013-12, Vol.41 (9), p.835-841

2013

Link zum Volltext

Verfügbarkeit prüfen

Reclassification of Diabetes Etiology in a Family With Multiple Diabetes Phenotypes

The journal of clinical endocrinology and metabolism, 2014-06, Vol.99 (6), p.E1067-E1071

2014

Link zum Volltext

Verfügbarkeit prüfen

Association Studies of Insulin Receptor Substrate 1 Gene (IRS1) Variants in Type 2 Diabetes Samples Enriched for Family History and Early Age of Onset

Diabetes (New York, N.Y.), 2004-12, Vol.53 (12), p.3319-3322

2004

Link zum Volltext

Verfügbarkeit prüfen

Genetic Variation in the Small Heterodimer Partner Gene and Young-Onset Type 2 Diabetes, Obesity, and Birth Weight in U.K. Subjects

Diabetes (New York, N.Y.), 2003-05, Vol.52 (5), p.1276-1279

2003

Link zum Volltext

Verfügbarkeit prüfen

Type 2 diabetes in the young: why we should worry

Practical diabetes (2011), 2014-07, Vol.31 (6), p.225-227

2014

Link zum Volltext

Verfügbarkeit prüfen

Treating Hypertension in Diabetic Nephropathy

Diabetes care, 2003-06, Vol.26 (6), p.1802-1805

2003

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 55

Suche als RSS-Feed

Aktive Filter

ThemaGenetics

KollektionJournals@Ovid

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(54)
Mit Volltextzugriff
(53)

Publikationsform

Artikel
(55)

Sprache

Englisch
(55)
Japanisch
(9)

Erscheinungsjahr

n.n

Thema

Humans
(31)
Science & Technology
(31)
Life Sciences & Biomedicine
(28)
Diabetes Mellitus, Type 2 - Genetics
(24)
Biological And Medical Sciences
(23)
Endocrinology & Metabolism
(22)
Medical Sciences
(22)
Adult
(20)
Diabetes
(19)
Diabetes. Impaired Glucose Tolerance
(19)
Endocrine Pancreas. Apud Cells
(19)
Endocrinopathies
(19)
Female
(19)
Etiopathogenesis. Screening. Investigations. Target Tissue Resistance
(16)
Male
(16)
Genetic Aspects
(14)
Middle Aged
(14)
Type 2 Diabetes
(12)
Genetic Predisposition To Disease
(9)
Hepatocyte Nuclear Factor 1-Alpha - Genetics
(9)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

High-Sensitivity CRP Discriminates HNF1A-MODY From Other Subtypes of Diabetes

Assessment of High-Sensitivity C-Reactive Protein Levels as Diagnostic Discriminator of Maturity-Onset Diabetes of the Young Due to HNF1A Mutations

Large-Scale Association Studies of Variants in Genes Encoding the Pancreatic β-Cell KATP Channel Subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) Confirm That the KCNJ11 E23K Variant Is Associated With Type 2 Diabetes

Diagnosis and management of maturity onset diabetes of the young (MODY)

Lixisenatide in type 1 diabetes: A randomised control trial of the effect of lixisenatide on post‐meal glucose excursions and glucagon in type 1 diabetes patients

Evaluation of Serum 1,5 Anhydroglucitol Levels as a Clinical Test to Differentiate Subtypes of Diabetes

Transdermal Blood Sampling for C-Peptide Is a Minimally Invasive, Reliable Alternative to Venous Sampling in Children and Adults With Type 1 Diabetes

Monogenic diabetes: old and new approaches to diagnosis

281-OR: Type 2 Diabetes Diagnosed between 16-30 Years in South Asian and White Individuals Is Phenotypically Similar

Plasma Fucosylated Glycans and C-Reactive Protein as Biomarkers of HNF1A-MODY in Young Adult-Onset Nonautoimmune Diabetes

Common Variant in the FTO Gene Is Associated with Body Mass Index and Predisposes to Childhood and Adult Obesity

Replication of Genome-Wide Association Signals in UK Samples Reveals Risk Loci for Type 2 Diabetes

Common Variants of the Hepatocyte Nuclear Factor-4α P2 Promoter Are Associated With Type 2 Diabetes in the U.K. Population

Interlaboratory evaluation of plasma N-glycan antennary fucosylation as a clinical biomarker for HNF1A-MODY using liquid chromatography methods

The Variable Number of Tandem Repeats Upstream of the Insulin Gene Is a Susceptibility Locus for Latent Autoimmune Diabetes in Adults

A Large-Scale Association Analysis of Common Variation of the HNF1α Gene With Type 2 Diabetes in the U.K. Caucasian Population

Altered cortisol metabolism in individuals with HNF1A‐MODY

1900-P: HNF1A Deficiency Leads to Perturbed Glucagon Secretion in Humans

Mutations in HNF1A Result in Marked Alterations of Plasma Glycan Profile

PAX6 mutation in association with ptosis, cataract, iris hypoplasia, corneal opacification and diabetes: a new variant of familial aniridia?

Reclassification of Diabetes Etiology in a Family With Multiple Diabetes Phenotypes

Association Studies of Insulin Receptor Substrate 1 Gene (IRS1) Variants in Type 2 Diabetes Samples Enriched for Family History and Early Age of Onset

Genetic Variation in the Small Heterodimer Partner Gene and Young-Onset Type 2 Diabetes, Obesity, and Birth Weight in U.K. Subjects

Type 2 diabetes in the young: why we should worry

Treating Hypertension in Diabetic Nephropathy

Aktive Filter

Suchergebnisse filtern