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Hypothyroxinaemia in preterm infants.
Krüger C, Dörr HG, Harms D. Krüger C, et al. Among authors: dorr hg. Eur J Pediatr. 1997 Apr;156(4):337. Eur J Pediatr. 1997. PMID: 9128824 No abstract available.
Genotype/phenotype correlations in 538 congenital adrenal hyperplasia patients from Germany and Austria: discordances in milder genotypes and in screened versus prescreening patients.
Riedl S, Röhl FW, Bonfig W, Brämswig J, Richter-Unruh A, Fricke-Otto S, Bettendorf M, Riepe F, Kriegshäuser G, Schönau E, Even G, Hauffa B, Dörr HG, Holl RW, Mohnike K; AQUAPE CAH Study Group. Riedl S, et al. Among authors: dorr hg. Endocr Connect. 2019 Feb 1;8(2):86-94. doi: 10.1530/EC-18-0281. Endocr Connect. 2019. PMID: 30620712 Free PMC article.
A de novo 7.6Mb tandem duplication of 14q32.2-qter associated with primordial short stature with neurosecretory growth hormone dysfunction, distinct facial anomalies and mild developmental delay.
Thiel CT, Dörr HG, Trautmann U, Hoyer J, Hofmann K, Kraus C, Ekici AB, Reis A, Rauch A. Thiel CT, et al. Among authors: dorr hg. Eur J Med Genet. 2008 Jul-Aug;51(4):362-7. doi: 10.1016/j.ejmg.2008.03.001. Epub 2008 Mar 20. Eur J Med Genet. 2008. PMID: 18434272
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.
220 results