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Absence of BiP co-chaperone DNAJC3 causes diabetes mellitus and multisystemic neurodegeneration.
Synofzik M, Haack TB, Kopajtich R, Gorza M, Rapaport D, Greiner M, Schönfeld C, Freiberg C, Schorr S, Holl RW, Gonzalez MA, Fritsche A, Fallier-Becker P, Zimmermann R, Strom TM, Meitinger T, Züchner S, Schüle R, Schöls L, Prokisch H. Synofzik M, et al. Among authors: freiberg c. Am J Hum Genet. 2014 Dec 4;95(6):689-97. doi: 10.1016/j.ajhg.2014.10.013. Epub 2014 Nov 20. Am J Hum Genet. 2014. PMID: 25466870 Free PMC article.
Clinical characteristics and cardiovascular risk profile in children and adolescents with latent autoimmune diabetes: Results from the German/Austrian prospective diabetes follow-up registry.
Welters A, Tittel SR, Reinehr T, Weghuber D, Wiegand S, Karges W, Freiberg C, Meissner T, Schloot NC, Holl RW. Welters A, et al. Among authors: freiberg c. Pediatr Diabetes. 2022 Dec;23(8):1602-1612. doi: 10.1111/pedi.13450. Epub 2022 Nov 27. Pediatr Diabetes. 2022. PMID: 36334008
Continuous glucose monitoring versus blood glucose monitoring for risk of severe hypoglycaemia and diabetic ketoacidosis in children, adolescents, and young adults with type 1 diabetes: a population-based study.
Karges B, Tittel SR, Bey A, Freiberg C, Klinkert C, Kordonouri O, Thiele-Schmitz S, Schröder C, Steigleder-Schweiger C, Holl RW. Karges B, et al. Among authors: freiberg c. Lancet Diabetes Endocrinol. 2023 May;11(5):314-323. doi: 10.1016/S2213-8587(23)00061-X. Epub 2023 Mar 30. Lancet Diabetes Endocrinol. 2023. PMID: 37004710
Reduction in Diabetic Ketoacidosis and Severe Hypoglycemia in Pediatric Type 1 Diabetes During the First Year of Continuous Glucose Monitoring: A Multicenter Analysis of 3,553 Subjects From the DPV Registry.
Tauschmann M, Hermann JM, Freiberg C, Papsch M, Thon A, Heidtmann B, Placzeck K, Agena D, Kapellen TM, Schenk B, Wolf J, Danne T, Rami-Merhar B, Holl RW; DPV Initiative. Tauschmann M, et al. Among authors: freiberg c. Diabetes Care. 2020 Mar;43(3):e40-e42. doi: 10.2337/dc19-1358. Epub 2020 Jan 22. Diabetes Care. 2020. PMID: 31969340 No abstract available.
Continuing role for classical cytogenetics: Case report of a boy with ring syndrome caused by complete ring chromosome 4 and review of literature.
Burgemeister AL, Daumiller E, Dietze-Armana I, Klett C, Freiberg C, Stark W, Lingen M, Centonze I, Rettenberger G, Mehnert K, Zirn B. Burgemeister AL, et al. Among authors: freiberg c. Am J Med Genet A. 2017 Mar;173(3):727-732. doi: 10.1002/ajmg.a.38063. Epub 2017 Jan 27. Am J Med Genet A. 2017. PMID: 28127864 Review.
53 results