Schulze E - Search Results

1

Steroid 21-hydroxylase mutations and 21-hydroxylase messenger ribonucleic acid expression in human adrenocortical tumors.

Beuschlein F, Schulze E, Mora P, Gensheimer HP, Maser-Gluth C, Allolio B, Reincke M. Beuschlein F, et al. Among authors: schulze e. J Clin Endocrinol Metab. 1998 Jul;83(7):2585-8. doi: 10.1210/jcem.83.7.4965. J Clin Endocrinol Metab. 1998. PMID: 9661649 Clinical Trial.

2

Metabolism of glucocorticoids and mineralocorticoids in patients with adrenal incidentalomas.

Maser-Gluth C, Reincke M, Allolio B, Schulze E. Maser-Gluth C, et al. Among authors: schulze e. Eur J Clin Invest. 2000 Dec;30 Suppl 3:83-6. doi: 10.1046/j.1365-2362.2000.0300s3083.x. Eur J Clin Invest. 2000. PMID: 11281375

3

Allele-dropout using PCR-based diagnosis for the splicing mutation in intron-2 of the CYP21B-gene: successful amplification with a Taq/Pwo-polymerase mixture.

Schulze E, Bettendorf M, Maser-Gluth C, Decker M, Schwabe U. Schulze E, et al. Endocr Res. 1998 Aug-Nov;24(3-4):637-41. doi: 10.3109/07435809809032662. Endocr Res. 1998. PMID: 9888552

4

Late diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Müssig K, Kaltenbach S, Maser-Gluth C, Hartmann MF, Wudy SA, Horger M, Gallwitz B, Raue F, Häring HU, Schulze E. Müssig K, et al. Among authors: schulze e. Exp Clin Endocrinol Diabetes. 2006 Apr;114(4):208-14. doi: 10.1055/s-2006-924072. Exp Clin Endocrinol Diabetes. 2006. PMID: 16705555

5

Machine learning approaches for phenotype-genotype mapping: predicting heterozygous mutations in the CYP21B gene from steroid profiles.

Prank K, Schulze E, Eckert O, Nattkemper TW, Bettendorf M, Maser-Gluth C, Sejnowski TJ, Grote A, Penner E, von Zur Mühlen A, Brabant G. Prank K, et al. Among authors: schulze e. Eur J Endocrinol. 2005 Aug;153(2):301-5. doi: 10.1530/eje.1.01957. Eur J Endocrinol. 2005. PMID: 16061837 Free PMC article.

6

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

Baumgartner-Parzer SM, Schulze E, Waldhäusl W, Pauschenwein S, Rondot S, Nowotny P, Meyer K, Frisch H, Waldhauser F, Vierhapper H. Baumgartner-Parzer SM, et al. Among authors: schulze e. J Clin Endocrinol Metab. 2001 Oct;86(10):4771-5. doi: 10.1210/jcem.86.10.7898. J Clin Endocrinol Metab. 2001. PMID: 11600539

7

21-Hydroxylase and 11beta-hydroxylase mutations in Romanian patients with classic congenital adrenal hyperplasia.

Grigorescu Sido A, Weber MM, Grigorescu Sido P, Clausmeyer S, Heinrich U, Schulze E. Grigorescu Sido A, et al. Among authors: schulze e. J Clin Endocrinol Metab. 2005 Oct;90(10):5769-73. doi: 10.1210/jc.2005-0379. Epub 2005 Jul 26. J Clin Endocrinol Metab. 2005. PMID: 16046588

8

Diagnosis of glucocorticoid-remediable aldosteronism in hypertensive children.

Kamrath C, Maser-Gluth C, Haag C, Schulze E. Kamrath C, et al. Among authors: schulze e. Horm Res Paediatr. 2011;76(2):93-8. doi: 10.1159/000326524. Epub 2011 May 27. Horm Res Paediatr. 2011. PMID: 21625068

9

Carboxyl-terminal mutations in 3beta-hydroxysteroid dehydrogenase type II cause severe salt-wasting congenital adrenal hyperplasia.

Welzel M, Wüstemann N, Simic-Schleicher G, Dörr HG, Schulze E, Shaikh G, Clayton P, Grötzinger J, Holterhus PM, Riepe FG. Welzel M, et al. Among authors: schulze e. J Clin Endocrinol Metab. 2008 Apr;93(4):1418-25. doi: 10.1210/jc.2007-1874. Epub 2008 Feb 5. J Clin Endocrinol Metab. 2008. PMID: 18252794

10

Mutational analysis and genotype-phenotype correlation in patients with classic 21-hydroxylase deficiency from transylvania (north-west Romania).

Grigorescu-Sido A, Schulze E, Grigorescu-Sido P, Heinrich U, Nistor T, Duncea I. Grigorescu-Sido A, et al. Among authors: schulze e. J Pediatr Endocrinol Metab. 2002 Nov-Dec;15(9):1505-14. doi: 10.1515/jpem.2002.15.9.1505. J Pediatr Endocrinol Metab. 2002. PMID: 12503858

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