Heinrich U - Search Results

1

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: heinrich u. 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

2

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: heinrich u. Horm Res. 2003;60(2):84-90. doi: 10.1159/000071876. Horm Res. 2003. PMID: 12876419

3

Three new 46,XX male patients: a clinical, cytogenetic and molecular analysis.

Grigorescu-Sido A, Heinrich U, Grigorescu-Sido P, Jauch A, Hager HD, Vogt PH, Duncea I, Bettendorf M. Grigorescu-Sido A, et al. Among authors: heinrich u. J Pediatr Endocrinol Metab. 2005 Feb;18(2):197-203. doi: 10.1515/jpem.2005.18.2.197. J Pediatr Endocrinol Metab. 2005. PMID: 15751609

4

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: heinrich u. 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

5

MRI findings and genotype analysis in patients with childhood onset growth hormone deficiency--correlation with severity of hypopituitarism.

Zimmermann A, Schenk JP, Grigorescu Sido P, Pfaffle R, Lazea C, Zimmermann T, Heinrich U, Weber MM, Bettendorf M. Zimmermann A, et al. Among authors: heinrich u. J Pediatr Endocrinol Metab. 2007 May;20(5):587-96. doi: 10.1515/jpem.2007.20.5.587. J Pediatr Endocrinol Metab. 2007. PMID: 17642419

6

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. Among authors: heinrich ue. Endocr Res. 1995 Feb-May;21(1-2):359-64. doi: 10.3109/07435809509030452. Endocr Res. 1995. PMID: 7588399

7

21-Deoxyaldosterone excretion in patients with primary aldosteronism and 21-hydroxylase deficiency.

Lewicka S, Winter J, Bige K, Bokkenheuser V, Vecsei P, Abdelhamid S, Heinrich U. Lewicka S, et al. Among authors: heinrich u. J Clin Endocrinol Metab. 1987 Apr;64(4):771-7. doi: 10.1210/jcem-64-4-771. J Clin Endocrinol Metab. 1987. PMID: 3493258

8

Longitudinal evaluation of salivary cortisol levels in full-term and preterm neonates.

Bettendorf M, Albers N, Bauer J, Heinrich UE, Linderkamp O, Maser-Gluth C. Bettendorf M, et al. Among authors: heinrich ue. Horm Res. 1998;50(6):303-8. doi: 10.1159/000023295. Horm Res. 1998. PMID: 9973669

9

Mucosal cytology in the determination of the pubertal status in girls.

Schmidt F, Grulich-Henn J, Heinrich UE, Bettendorf M. Schmidt F, et al. Horm Res. 2002;58(5):223-8. doi: 10.1159/000066264. Horm Res. 2002. PMID: 12401941

10

Metacarpal index in short stature before and during growth hormone treatment.

Bettendorf M, Graf K, Nelle M, Heinrich UE, Tröger J. Bettendorf M, et al. Among authors: heinrich ue. Arch Dis Child. 1998 Aug;79(2):165-8. doi: 10.1136/adc.79.2.165. Arch Dis Child. 1998. PMID: 9797601 Free PMC article.

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