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An Integrated clinical pathway for diagnosis, treatment and care of rare diseases: model, operating procedures, and results of the project TRANSLATE-NAMSE funded by the German Federal Joint Committee.
Choukair D, Hauck F, Bettendorf M, Krude H, Klein C, Bäumer T, Berner R, Lee-Kirsch MA, Grasemann C, Burgard P, Hoffmann GF. Choukair D, et al. Among authors: bettendorf m. Orphanet J Rare Dis. 2021 Nov 12;16(1):474. doi: 10.1186/s13023-021-02092-w. Orphanet J Rare Dis. 2021. PMID: 34772435 Free PMC article.
Guanine nucleotide-binding protein α subunit hypofunction in children with short stature and disproportionate shortening of the 4th and 5th metacarpals.
Inta IM, Choukair D, Bender S, Kneppo C, Knauer-Fischer S, Meyenburg K, Ivandic B, Pfister SM, Bettendorf M. Inta IM, et al. Among authors: bettendorf m. Horm Res Paediatr. 2014;81(3):196-203. doi: 10.1159/000356928. Epub 2014 Jan 25. Horm Res Paediatr. 2014. PMID: 24481334 Free article. Clinical Trial.
Risk Factors for Childhood Overweight and Obesity in Ukraine and Germany.
Yakovenko V, Henn L, Bettendorf M, Zelinska N, Soloviova G, Hoffmann GF, Grulich-Henn J. Yakovenko V, et al. Among authors: bettendorf m. J Clin Res Pediatr Endocrinol. 2019 Sep 3;11(3):247-252. doi: 10.4274/jcrpe.galenos.2019.2018.0157. Epub 2019 Jan 11. J Clin Res Pediatr Endocrinol. 2019. PMID: 30630809 Free PMC article.
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: bettendorf m. J Pediatr Endocrinol Metab. 2019 Mar 26;32(3):259-267. doi: 10.1515/jpem-2018-0298. J Pediatr Endocrinol Metab. 2019. PMID: 30817301
116 results