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Page 1
An expanded clinical spectrum of hypoinsulinaemic hypoketotic hypoglycaemia.
Welters A, Leiter SM, Bachmann N, Bergmann C, Hoermann H, Korsch E, Meissner T, Payne F, Williams R, Hussain K, Semple RK, Kummer S. Welters A, et al. Among authors: korsch e. Orphanet J Rare Dis. 2023 Nov 16;18(1):360. doi: 10.1186/s13023-023-02954-5. Orphanet J Rare Dis. 2023. PMID: 37974153 Free PMC article.
[Aphallia - report of two cases].
Hagelschuer P, Mack-Detlefsen B, Korsch E, Ekamp A, Boemers TM. Hagelschuer P, et al. Among authors: korsch e. Urologe A. 2020 Jul;59(7):825-828. doi: 10.1007/s00120-020-01244-3. Urologe A. 2020. PMID: 32472223 German.
MKRN3 mutations in familial central precocious puberty.
Schreiner F, Gohlke B, Hamm M, Korsch E, Woelfle J. Schreiner F, et al. Among authors: korsch e. Horm Res Paediatr. 2014;82(2):122-6. doi: 10.1159/000362815. Epub 2014 Jul 5. Horm Res Paediatr. 2014. PMID: 25011910
Are H19 variants associated with Silver-Russell syndrome?
Schönherr N, Binder G, Korsch E, Kämmerer E, Wollmann HA, Eggermann T. Schönherr N, et al. Among authors: korsch e. J Pediatr Endocrinol Metab. 2008 Oct;21(10):985-93. doi: 10.1515/jpem.2008.21.10.985. J Pediatr Endocrinol Metab. 2008. PMID: 19209620
Mosaic tetrasomy 14pterq13.1: longitudinal study.
Schwanitz G, Korsch E, Kremens-Korsch U, Ahlbory K, Gamerdinger U, Heidrich-Kaul C, Schubert R, Spengler S, Eggermann T. Schwanitz G, et al. Among authors: korsch e. Eur J Med Genet. 2011 Jul-Aug;54(4):e465-7. doi: 10.1016/j.ejmg.2011.03.003. Epub 2011 Mar 21. Eur J Med Genet. 2011. PMID: 21420515 No abstract available.
36 results