دورية أكاديمية

Treating hypercholesterinemia in a patient with maternally inherited diabetes and deafness (MIDD) by the proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitor alirocumab.

التفاصيل البيبلوغرافية
العنوان: Treating hypercholesterinemia in a patient with maternally inherited diabetes and deafness (MIDD) by the proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitor alirocumab.
المؤلفون: Schultes, Bernd, Ernst, Barbara, Schmid, Sebastian M.
المصدر: Acta Diabetologica; Nov2021, Vol. 58 Issue 11, p1575-1577, 3p
مصطلحات موضوعية: INSULIN derivatives, DIABETES, MELAS syndrome, SUBTILISINS
مستخلص: Keywords: MIDD; PCSK9 inhibitors; Hypercholesterinemia; Arteriosclerotic cardiovascular disease; Mitochondrial EN MIDD PCSK9 inhibitors Hypercholesterinemia Arteriosclerotic cardiovascular disease Mitochondrial 1575 1577 3 10/13/21 20211101 NES 211101 This article belongs to the topical collection Pregnancy and Diabetes, managed by Antonio Secchi and Marina Scavini. Proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors have been shown to markedly lower LDL-C levels in patients with T2DM [[4]] and could be a valuable therapeutic option also in patients with MIDD. [Extracted from the article]
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قاعدة البيانات: Complementary Index
الوصف
تدمد:09405429
DOI:10.1007/s00592-021-01776-w