Schulze E - Search Results

1

Clinical Features and Response to Treatment of Prolactinomas in Children and Adolescents: A Retrospective Single-Centre Analysis and Review of the Literature.

Breil T, Lorz C, Choukair D, Mittnacht J, Inta I, Klose D, Jesser J, Schulze E, Bettendorf M. Breil T, et al. Among authors: schulze e. Horm Res Paediatr. 2018;89(3):157-165. doi: 10.1159/000486280. Epub 2018 Feb 16. Horm Res Paediatr. 2018. PMID: 29455199 Review.

2

Typical characteristics of children with congenital adrenal hyperplasia due to 11β-hydroxylase deficiency: a single-centre experience and review of the literature.

Breil T, Yakovenko V, Inta I, Choukair D, Klose D, Mittnacht J, Schulze E, Alrajab A, Grulich-Henn J, Bettendorf M. Breil T, et al. Among authors: schulze e. J Pediatr Endocrinol Metab. 2019 Mar 26;32(3):259-267. doi: 10.1515/jpem-2018-0298. J Pediatr Endocrinol Metab. 2019. PMID: 30817301

3

Screening for Pax8 mutations in patients with congenital hypothyroidism in South-West Germany.

Lanzerath K, Bettendorf M, Haag C, Kneppo C, Schulze E, Grulich-Henn J. Lanzerath K, et al. Among authors: schulze e. Horm Res. 2006;66(2):96-100. doi: 10.1159/000093799. Epub 2006 Jun 7. Horm Res. 2006. PMID: 16763387

4

Growth analysis in patients with 21-hydroxylase deficiency influence of glucocorticoid dosage, age at diagnosis, phenotype and genotype on growth and height outcome.

Grigorescu-Sido A, Bettendorf M, Schulze E, Duncea I, Heinrich U. Grigorescu-Sido A, et al. Among authors: schulze e. Horm Res. 2003;60(2):84-90. doi: 10.1159/000071876. Horm Res. 2003. PMID: 12876419

5

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

6

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

7

Divergence between genotype and phenotype in relatives of patients with the intron 2 mutation of steroid-21-hydroxylase.

Schulze E, Scharer G, Rogatzki A, Priebe L, Lewicka S, Bettendorf M, Hoepffner W, Heinrich UE, Schwabe U. Schulze E, et al. Endocr Res. 1995 Feb-May;21(1-2):359-64. doi: 10.3109/07435809509030452. Endocr Res. 1995. PMID: 7588399

8

Activating mutations in the calcium-sensing receptor: genetic and clinical spectrum in 25 patients with autosomal dominant hypocalcaemia - a German survey.

Raue F, Pichl J, Dörr HG, Schnabel D, Heidemann P, Hammersen G, Jaursch-Hancke C, Santen R, Schöfl C, Wabitsch M, Haag C, Schulze E, Frank-Raue K. Raue F, et al. Among authors: schulze e. Clin Endocrinol (Oxf). 2011 Dec;75(6):760-5. doi: 10.1111/j.1365-2265.2011.04142.x. Clin Endocrinol (Oxf). 2011. PMID: 21645025

9

Alterations in lipid and carbohydrate metabolism in patients with classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Zimmermann A, Grigorescu-Sido P, AlKhzouz C, Patberg K, Bucerzan S, Schulze E, Zimmermann T, Rossmann H, Geiss HC, Lackner KJ, Weber MM. Zimmermann A, et al. Among authors: schulze e. Horm Res Paediatr. 2010;74(1):41-9. doi: 10.1159/000313368. Epub 2010 Apr 15. Horm Res Paediatr. 2010. PMID: 20395657

10

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.

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