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Reduction of both number and proliferative activity of human endothelial progenitor cells in obesity

International Journal of Obesity, 2010-04, Vol.34 (4), p.687-700

2010

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Duplications of the Functional CYP21A2 Gene Are Primarily Restricted to Q318X Alleles: Evidence for a Founder Effect

The journal of clinical endocrinology and metabolism, 2009-10, Vol.94 (10), p.3954-3958

2009

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Carrier Frequency of Congenital Adrenal Hyperplasia (21-Hydroxylase Deficiency) in a Middle European Population

The journal of clinical endocrinology and metabolism, 2005-02, Vol.90 (2), p.775-778

2005

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Fasting and postprandial liver glycogen content in patients with type 1 diabetes mellitus after successful pancreas-kidney transplantation with systemic venous insulin delivery

Clinical endocrinology (Oxford), 2014-02, Vol.80 (2), p.208-213

2014

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Polymorphisms in Exon 13 and Intron 14 of the RET Protooncogene: Genetic Modifiers of Medullary Thyroid Carcinoma?

The journal of clinical endocrinology and metabolism, 2005-11, Vol.90 (11), p.6232-6236

2005

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Suppression of plasma free fatty acids reduces myocardial lipid content and systolic function in type 2 diabetes

Nutrition, metabolism, and cardiovascular diseases, 2016-05, Vol.26 (5), p.387-392

2016

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Mutational spectrum of steroid 21-hydroxylase and the genotype-phenotype association in Middle European patients with congenital adrenal hyperplasia

European journal of endocrinology, 2005-07, Vol.153 (1), p.99-106

2005

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Modulation by leptin of proliferation and apoptosis in vascular endothelial cells

International Journal of Obesity, 2002-04, Vol.26 (4), p.577-580

2002

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Early Diagnosis and Curative Therapy of Medullary Thyroid Carcinoma by Routine Measurement of Serum Calcitonin in Patients with Thyroid Disorders

Thyroid (New York, N.Y.), 2005-11, Vol.15 (11), p.1267-1272

2005

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Insulin does not regulate glucose transport and metabolism in human endothelium

European journal of clinical investigation, 2007-08, Vol.37 (8), p.643-650

2007

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Adolescent Risk Behavior and Self-Regulation: A Cybernetic Perspective

1st Edition 2021, 2021

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Cloning and molecular characterization of Dashurin encoded by C20orf116, a PCI-domain containing protein

Biochimica et biophysica acta, 2010-04, Vol.1800 (4), p.430-438

2010

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Predisposition for de Novo Gene Aberrations in the Offspring of Mothers with a Duplicated CYP21A2 Gene

The journal of clinical endocrinology and metabolism, 2007-03, Vol.92 (3), p.1164-1167

2007

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High-glucose--triggered apoptosis in cultured endothelial cells

Diabetes (New York, N.Y.), 1995-11, Vol.44 (11), p.1323-1327

1995

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Involvement of epigenetic mechanisms in regulating expression of the calcium sensing receptor in colorectal cancer

Bone (New York, N.Y.), 2012-12, Vol.51 (6), p.S23-S23

2012

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Increased heterogeneity of bone matrix mineralization in a patient with familial hypercalcaemic hypocalciuria due to the loss of function of the calcium sensing receptor

Bone (New York, N.Y.), 2012-12, Vol.51 (6), p.S15-S16

2012

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Mutational spectrum of the steroid 21-hydroxylase gene in Austria : Identification of a novel missense mutation

The journal of clinical endocrinology and metabolism, 2001-10, Vol.86 (10), p.4771-4775

2001

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Increased prevalence of heterozygous 21-OH germline mutations in patients with adrenal incidentalomas

Clinical endocrinology (Oxford), 2002-06, Vol.56 (6), p.811-816

2002

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Frequency of RET Proto-Oncogene Mutations in Patients with Normal and with Moderately Elevated Pentagastrin-Stimulated Serum Concentrations of Calcitonin

Thyroid (New York, N.Y.), 2004-08, Vol.14 (8), p.58-583

2004

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The endothelium as a metabolic and endocrine organ: its relation with insulin resistance

Experimental and clinical endocrinology & diabetes, 2001, Vol.109 Suppl 2 (Suppl 2), p.S166-S179

2001

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Severe hypertriglyceridemia and its correlation with clinical atherosclerosis and pancreatitis investigated in beta-quantification

European heart journal, 2023-11, Vol.44 (Supplement_2)

2023

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Thiazolidinediones inhibit proliferation of microvascular and macrovascular cells by a PPARγ-independent mechanism

Diabetologia, 2005-03, Vol.48 (3), p.586-594

2005

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Mutational Spectrum of the Steroid 21-Hydroxylase Gene in Austria: Identification of a Novel Missense Mutation

The journal of clinical endocrinology and metabolism, 2001-10, Vol.86 (10), p.4771-4775

2001

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Analysis of routine molecular genetic diagnostics of familial hypercholesterolemia at tertiary care lipid clinics

European heart journal, 2023-11, Vol.44 (Supplement_2)

2023

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A Rare Duplicated 21-Hydroxylase Haplotype and a de Novo Mutation: A Family Analysis

The journal of clinical endocrinology and metabolism, 2003-06, Vol.88 (6), p.2794-2796

2003

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Reduction of both number and proliferative activity of human endothelial progenitor cells in obesity

Duplications of the Functional CYP21A2 Gene Are Primarily Restricted to Q318X Alleles: Evidence for a Founder Effect

Carrier Frequency of Congenital Adrenal Hyperplasia (21-Hydroxylase Deficiency) in a Middle European Population

Fasting and postprandial liver glycogen content in patients with type 1 diabetes mellitus after successful pancreas-kidney transplantation with systemic venous insulin delivery

Polymorphisms in Exon 13 and Intron 14 of the RET Protooncogene: Genetic Modifiers of Medullary Thyroid Carcinoma?

Suppression of plasma free fatty acids reduces myocardial lipid content and systolic function in type 2 diabetes

Mutational spectrum of steroid 21-hydroxylase and the genotype-phenotype association in Middle European patients with congenital adrenal hyperplasia

Modulation by leptin of proliferation and apoptosis in vascular endothelial cells

Early Diagnosis and Curative Therapy of Medullary Thyroid Carcinoma by Routine Measurement of Serum Calcitonin in Patients with Thyroid Disorders

Insulin does not regulate glucose transport and metabolism in human endothelium

Adolescent Risk Behavior and Self-Regulation: A Cybernetic Perspective

Cloning and molecular characterization of Dashurin encoded by C20orf116, a PCI-domain containing protein

Predisposition for de Novo Gene Aberrations in the Offspring of Mothers with a Duplicated CYP21A2 Gene

High-glucose--triggered apoptosis in cultured endothelial cells

Involvement of epigenetic mechanisms in regulating expression of the calcium sensing receptor in colorectal cancer

Increased heterogeneity of bone matrix mineralization in a patient with familial hypercalcaemic hypocalciuria due to the loss of function of the calcium sensing receptor

Mutational spectrum of the steroid 21-hydroxylase gene in Austria : Identification of a novel missense mutation

Increased prevalence of heterozygous 21-OH germline mutations in patients with adrenal incidentalomas

Frequency of RET Proto-Oncogene Mutations in Patients with Normal and with Moderately Elevated Pentagastrin-Stimulated Serum Concentrations of Calcitonin

The endothelium as a metabolic and endocrine organ: its relation with insulin resistance

Severe hypertriglyceridemia and its correlation with clinical atherosclerosis and pancreatitis investigated in beta-quantification

Thiazolidinediones inhibit proliferation of microvascular and macrovascular cells by a PPARγ-independent mechanism

Mutational Spectrum of the Steroid 21-Hydroxylase Gene in Austria: Identification of a Novel Missense Mutation

Analysis of routine molecular genetic diagnostics of familial hypercholesterolemia at tertiary care lipid clinics

A Rare Duplicated 21-Hydroxylase Haplotype and a de Novo Mutation: A Family Analysis

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