Dörr HG - Search Results

1

Caring for a Child with Congenital Adrenal Hyperplasia Diagnosed by Newborn Screening: Parental Health-Related Quality of Life, Coping Patterns, and Needs.

Rautmann L, Witt S, Theiding C, Odenwald B, Nennstiel-Ratzel U, Dörr HG, Quitmann JH. Rautmann L, et al. Among authors: dorr hg. Int J Environ Res Public Health. 2023 Mar 3;20(5):4493. doi: 10.3390/ijerph20054493. Int J Environ Res Public Health. 2023. PMID: 36901502 Free PMC article.

2

Children with classic congenital adrenal hyperplasia experience salt loss and hypoglycemia: evaluation of adrenal crises during the first 6 years of life.

Odenwald B, Nennstiel-Ratzel U, Dörr HG, Schmidt H, Wildner M, Bonfig W. Odenwald B, et al. Among authors: dorr hg. Eur J Endocrinol. 2016 Feb;174(2):177-86. doi: 10.1530/EJE-15-0775. Epub 2015 Nov 12. Eur J Endocrinol. 2016. PMID: 26563979

3

Psychometric properties of the quality of life in short statured youth (QoLISSY) questionnaire within the course of growth hormone treatment.

Bloemeke J, Silva N, Bullinger M, Witt S, Dörr HG, Quitmann J. Bloemeke J, et al. Among authors: dorr hg. Health Qual Life Outcomes. 2019 Mar 18;17(1):49. doi: 10.1186/s12955-019-1118-9. Health Qual Life Outcomes. 2019. PMID: 30885197 Free PMC article.

4

Quality of Life of Short-Statured Children Born Small for Gestational Age or Idiopathic Growth Hormone Deficiency Within 1 Year of Growth Hormone Treatment.

Quitmann J, Bloemeke J, Silva N, Bullinger M, Witt S, Akkurt I, Dunstheimer D, Vogel C, Böttcher V, Kuhnle Krahl U, Bettendorf M, Schönau E, Fricke-Otto S, Keller A, Mohnike K, Dörr HG. Quitmann J, et al. Among authors: dorr hg. Front Pediatr. 2019 Apr 29;7:164. doi: 10.3389/fped.2019.00164. eCollection 2019. Front Pediatr. 2019. PMID: 31111024 Free PMC article.

5

Intellectual outcome, motor skills and BMI of children with congenital hypothyroidism: a population-based study.

Arenz S, Nennstiel-Ratzel U, Wildner M, Dörr HG, von Kries R. Arenz S, et al. Among authors: dorr hg. Acta Paediatr. 2008 Apr;97(4):447-50. doi: 10.1111/j.1651-2227.2008.00702.x. Epub 2008 Mar 7. Acta Paediatr. 2008. PMID: 18331367

6

Value of direct measurement of active renin concentrations in congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Krüger C, Höper K, Weissörtel R, Hensen J, Dörr HG. Krüger C, et al. Among authors: dorr hg. Eur J Pediatr. 1996 Oct;155(10):858-61. doi: 10.1007/BF02282834. Eur J Pediatr. 1996. PMID: 8891554

7

Androglottia in a young female adolescent with congenital adrenal hyperplasia and 21-hydroxylase deficiency.

Fürst-Recktenwald S, Dörr HG, Rosanowski F. Fürst-Recktenwald S, et al. Among authors: dorr hg. J Pediatr Endocrinol Metab. 2000 Jul-Aug;13(7):959-62. doi: 10.1515/jpem.2000.13.7.959. J Pediatr Endocrinol Metab. 2000. PMID: 10968487

8

Serum cortisol and cortisone levels in newborns with congenital adrenal hyperplasia before the start of therapy.

Dötsch J, Hohenberger I, Riepe FG, Sippell WG, Dörr HG. Dötsch J, et al. Among authors: dorr hg. J Endocrinol Invest. 2005 May;28(5):413-6. doi: 10.1007/BF03347220. J Endocrinol Invest. 2005. PMID: 16075923

9

Anorexia nervosa in congenital adrenal hyperplasia: long-term follow-up of 4 cases.

Brand M, Schoof E, Partsch C-J, Peter M, Hoepffner W, Dörr HG, Sippell WG. Brand M, et al. Among authors: dorr hg. Exp Clin Endocrinol Diabetes. 2000;108(6):430-5. doi: 10.1055/s-2000-8139. Exp Clin Endocrinol Diabetes. 2000. PMID: 11026757

10

Naltrexone as a diagnostic tool to distinguish between hyperandrogenemic and hypothalamic ovarian failure in females with congenital adrenal hyperplasia due to 21-hydroxylase-deficiency (CAH).

Böttcher B, Dörr HG, Wildt L. Böttcher B, et al. Among authors: dorr hg. Eur J Obstet Gynecol Reprod Biol. 2014 Sep;180:153-6. doi: 10.1016/j.ejogrb.2014.06.007. Epub 2014 Jun 24. Eur J Obstet Gynecol Reprod Biol. 2014. PMID: 25065344

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