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Page 1
Comorbidity of type 1 diabetes and juvenile idiopathic arthritis.
Hermann G, Thon A, Mönkemöller K, Lilienthal E, Klinkert C, Holder M, Hörtenhuber T, Vogel-Gerlicher P, Haberland H, Schebek M, Holl RW; Diabetes Patienten Verlaufsdokumentation-initiative; Federal Ministry of Education and Research Competence Network Diabetes Mellitus. Hermann G, et al. Among authors: schebek m. J Pediatr. 2015 Apr;166(4):930-5.e1-3. doi: 10.1016/j.jpeds.2014.12.026. Epub 2015 Jan 29. J Pediatr. 2015. PMID: 25641245
Effectiveness and safety of long-term treatment with sulfonylureas in patients with neonatal diabetes due to KCNJ11 mutations: an international cohort study.
Bowman P, Sulen Å, Barbetti F, Beltrand J, Svalastoga P, Codner E, Tessmann EH, Juliusson PB, Skrivarhaug T, Pearson ER, Flanagan SE, Babiker T, Thomas NJ, Shepherd MH, Ellard S, Klimes I, Szopa M, Polak M, Iafusco D, Hattersley AT, Njølstad PR; Neonatal Diabetes International Collaborative Group. Bowman P, et al. Lancet Diabetes Endocrinol. 2018 Aug;6(8):637-646. doi: 10.1016/S2213-8587(18)30106-2. Epub 2018 Jun 4. Lancet Diabetes Endocrinol. 2018. PMID: 29880308 Free PMC article.
Comparative meta-analysis of Kabuki syndrome with and without hyperinsulinaemic hypoglycaemia.
Hoermann H, El-Rifai O, Schebek M, Lodefalk M, Brusgaard K, Bachmann N, Bergmann C, Roeper M, Welters A, Salimi Dafsari R, Blankenstein O, Mayatepek E, Christesen H, Meissner T, Kummer S. Hoermann H, et al. Among authors: schebek m. Clin Endocrinol (Oxf). 2020 Sep;93(3):346-354. doi: 10.1111/cen.14267. Epub 2020 Jul 15. Clin Endocrinol (Oxf). 2020. PMID: 32533869
Long-term Follow-up of Glycemic and Neurological Outcomes in an International Series of Patients With Sulfonylurea-Treated ABCC8 Permanent Neonatal Diabetes.
Bowman P, Mathews F, Barbetti F, Shepherd MH, Sanchez J, Piccini B, Beltrand J, Letourneau-Freiberg LR, Polak M, Greeley SAW, Rawlins E, Babiker T, Thomas NJ, De Franco E, Ellard S, Flanagan SE, Hattersley AT; Neonatal Diabetes International Collaborative Group. Bowman P, et al. Diabetes Care. 2021 Jan;44(1):35-42. doi: 10.2337/dc20-1520. Epub 2020 Nov 12. Diabetes Care. 2021. PMID: 33184150 Free PMC article.
Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood.
Edghill EL, Flanagan SE, Patch AM, Boustred C, Parrish A, Shields B, Shepherd MH, Hussain K, Kapoor RR, Malecki M, MacDonald MJ, Støy J, Steiner DF, Philipson LH, Bell GI; Neonatal Diabetes International Collaborative Group; Hattersley AT, Ellard S. Edghill EL, et al. Diabetes. 2008 Apr;57(4):1034-42. doi: 10.2337/db07-1405. Epub 2007 Dec 27. Diabetes. 2008. PMID: 18162506 Free PMC article.
Success of the German Cystic Fibrosis Registry.
Naehrlich L, Burkhart M; Registry Working Group of the German CF Registry. Naehrlich L, et al. Pharmacoepidemiol Drug Saf. 2025 Jan;34(1):e70076. doi: 10.1002/pds.70076. Pharmacoepidemiol Drug Saf. 2025. PMID: 39775994 Free PMC article.
Every CFTR variant counts - Target-capture based next-generation-sequencing for molecular diagnosis in the German CF Registry.
Ahting S, Nährlich L, Held I, Henn C, Krill A, Landwehr K, Meister J, Nährig S, Nolde A, Remke K, Ruppel R, Sauer-Heilborn A, Schebek M, Schopper G, Schulte-Hubbert B, Schwarz C, Smaczny C, Wege S, Hentschel J; Registry Working Group of the German CF Registry. Ahting S, et al. Among authors: schebek m. J Cyst Fibros. 2024 Jul;23(4):774-781. doi: 10.1016/j.jcf.2023.10.009. Epub 2023 Oct 21. J Cyst Fibros. 2024. PMID: 37867076
13 results