S M Baumgartner-Parzer

Summary

Affiliation: Medical University of Vienna
Country: Austria

Publications

  1. ncbi request reprint Regulation of the calcium-sensing receptor expression by 1,25-dihydroxyvitamin D3, interleukin-6, and tumor necrosis factor alpha in colon cancer cells
    Irfete S Fetahu
    Department of Pathophysiology and Allergy Research, Medical University of Vienna, Wahringer Gurtel 18 20, Vienna, Austria Electronic address
    J Steroid Biochem Mol Biol 144:228-31. 2014
  2. ncbi request reprint Carrier frequency of congenital adrenal hyperplasia (21-hydroxylase deficiency) in a middle European population
    S M Baumgartner-Parzer
    Department of Internal Medicine III, Medical University of Vienna, A 1090 Vienna, Austria
    J Clin Endocrinol Metab 90:775-8. 2005
  3. ncbi request reprint Polymorphisms in exon 13 and intron 14 of the RET protooncogene: genetic modifiers of medullary thyroid carcinoma?
    S M Baumgartner-Parzer
    Department of Internal Medicine III, Division of Endocrinology and Metabolism, Waehringer Guertel 18 20, A 1090 Vienna, Austria
    J Clin Endocrinol Metab 90:6232-6. 2005
  4. ncbi request reprint Predisposition for de novo gene aberrations in the offspring of mothers with a duplicated CYP21A2 gene
    S M Baumgartner-Parzer
    Department of Internal Medicine III, Division of Endocrinology and Metabolism, Waehringer Guertel 18 20, A 1090 Vienna, Austria
    J Clin Endocrinol Metab 92:1164-7. 2007
  5. ncbi request reprint Mutational spectrum of the steroid 21-hydroxylase gene in Austria: identification of a novel missense mutation
    S M Baumgartner-Parzer
    Department of Internal Medicine III, Division of Endocrinology and Metabolism, University of Vienna, Waeringer Guertel 18 20, A 1090 Vienna, Austria
    J Clin Endocrinol Metab 86:4771-5. 2001
  6. ncbi request reprint A rare duplicated 21-hydroxylase haplotype and a de novo mutation: a family analysis
    S M Baumgartner-Parzer
    Department of Internal Medicine III, Division of Clinical Endocrinology and Metabolism, University of Vienna, A 1090 Vienna, Austria
    J Clin Endocrinol Metab 88:2794-6. 2003
  7. ncbi request reprint Duplications of the functional CYP21A2 gene are primarily restricted to Q318X alleles: evidence for a founder effect
    S Kleinle
    Department of Internal Medicine III, Division of Clinical Endocrinology and Metabolism, Medical University of Vienna, A 1090 Vienna, Austria
    J Clin Endocrinol Metab 94:3954-8. 2009
  8. ncbi request reprint Increased prevalence of heterozygous 21-OH germline mutations in patients with adrenal incidentalomas
    S M Baumgartner-Parzer
    Department of Internal Medicine III, University of Vienna, Austria
    Clin Endocrinol (Oxf) 56:811-6. 2002
  9. ncbi request reprint Reduction of both number and proliferative activity of human endothelial progenitor cells in obesity
    K Tobler
    Department of Internal Medicine III, Clinical Division of Endocrinology and Metabolism, Medical University of Vienna, Vienna, Austria
    Int J Obes (Lond) 34:687-700. 2010
  10. ncbi request reprint Determination of plasma ET-1 by RIA--risks and limitations
    S M Baumgartner-Parzer
    Department of Internal Medicine III, University of Vienna, Austria
    Horm Metab Res 30:633-5. 1998

Collaborators

Detail Information

Publications12

  1. ncbi request reprint Regulation of the calcium-sensing receptor expression by 1,25-dihydroxyvitamin D3, interleukin-6, and tumor necrosis factor alpha in colon cancer cells
    Irfete S Fetahu
    Department of Pathophysiology and Allergy Research, Medical University of Vienna, Wahringer Gurtel 18 20, Vienna, Austria Electronic address
    J Steroid Biochem Mol Biol 144:228-31. 2014
    ..5-fold). Our data demonstrated transcriptional and translational activation of the CaSR by 1,25D3, TNFα, and IL-6 in a time- and cell line-dependent manner. This article is part of a Special Issue entitled '16th Vitamin D Workshop'. ..
  2. ncbi request reprint Carrier frequency of congenital adrenal hyperplasia (21-hydroxylase deficiency) in a middle European population
    S M Baumgartner-Parzer
    Department of Internal Medicine III, Medical University of Vienna, A 1090 Vienna, Austria
    J Clin Endocrinol Metab 90:775-8. 2005
    ..In conclusion, the observed CAH carrier frequency of 9.5% suggests a higher prevalence of CAH heterozygosity in a middle European population than hitherto estimated independently of the individuals' Yugoslav or non-Yugoslav origin...
  3. ncbi request reprint Polymorphisms in exon 13 and intron 14 of the RET protooncogene: genetic modifiers of medullary thyroid carcinoma?
    S M Baumgartner-Parzer
    Department of Internal Medicine III, Division of Endocrinology and Metabolism, Waehringer Guertel 18 20, A 1090 Vienna, Austria
    J Clin Endocrinol Metab 90:6232-6. 2005
    ....
  4. ncbi request reprint Predisposition for de novo gene aberrations in the offspring of mothers with a duplicated CYP21A2 gene
    S M Baumgartner-Parzer
    Department of Internal Medicine III, Division of Endocrinology and Metabolism, Waehringer Guertel 18 20, A 1090 Vienna, Austria
    J Clin Endocrinol Metab 92:1164-7. 2007
    ..Whereas so far, only heterozygous deletions of the CYP21A1P pseudogene were seen as premutations for de novo aberrations, the present report addresses such a predisposing role for parental duplicated CYP21A2 genes...
  5. ncbi request reprint Mutational spectrum of the steroid 21-hydroxylase gene in Austria: identification of a novel missense mutation
    S M Baumgartner-Parzer
    Department of Internal Medicine III, Division of Endocrinology and Metabolism, University of Vienna, Waeringer Guertel 18 20, A 1090 Vienna, Austria
    J Clin Endocrinol Metab 86:4771-5. 2001
    ....
  6. ncbi request reprint A rare duplicated 21-hydroxylase haplotype and a de novo mutation: a family analysis
    S M Baumgartner-Parzer
    Department of Internal Medicine III, Division of Clinical Endocrinology and Metabolism, University of Vienna, A 1090 Vienna, Austria
    J Clin Endocrinol Metab 88:2794-6. 2003
    ..This family analysis highlights the complexity of the CYP21/CYP21P(pseudogene) loci and the difficulties of 21-OH genotyping...
  7. ncbi request reprint Duplications of the functional CYP21A2 gene are primarily restricted to Q318X alleles: evidence for a founder effect
    S Kleinle
    Department of Internal Medicine III, Division of Clinical Endocrinology and Metabolism, Medical University of Vienna, A 1090 Vienna, Austria
    J Clin Endocrinol Metab 94:3954-8. 2009
    ....
  8. ncbi request reprint Increased prevalence of heterozygous 21-OH germline mutations in patients with adrenal incidentalomas
    S M Baumgartner-Parzer
    Department of Internal Medicine III, University of Vienna, Austria
    Clin Endocrinol (Oxf) 56:811-6. 2002
    ..We therefore performed an analysis of the prevalence of 21-OH germline mutations in patients with non-functional adrenal incidentalomas...
  9. ncbi request reprint Reduction of both number and proliferative activity of human endothelial progenitor cells in obesity
    K Tobler
    Department of Internal Medicine III, Clinical Division of Endocrinology and Metabolism, Medical University of Vienna, Vienna, Austria
    Int J Obes (Lond) 34:687-700. 2010
    ....
  10. ncbi request reprint Determination of plasma ET-1 by RIA--risks and limitations
    S M Baumgartner-Parzer
    Department of Internal Medicine III, University of Vienna, Austria
    Horm Metab Res 30:633-5. 1998
    ..Thus, this study clearly documents that ET-1 concentrations measured in plasma samples represent apparent concentrations which have to be interpreted with caution...
  11. ncbi request reprint Thiazolidinediones inhibit proliferation of microvascular and macrovascular cells by a PPARgamma-independent mechanism
    M Artwohl
    Department of Internal Medicine III, Clinical Division of Endocrinology and Metabolism, Medical University of Vienna, Vienna, Austria
    Diabetologia 48:586-94. 2005
    ....
  12. ncbi request reprint Mutational spectrum of steroid 21-hydroxylase and the genotype-phenotype association in Middle European patients with congenital adrenal hyperplasia
    V Dolzan
    Institute of Biochemistry, Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia
    Eur J Endocrinol 153:99-106. 2005
    ....