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Impact of Mutational Testing on the Diagnosis and Management of Patients with Cytologically Indeterminate Thyroid Nodules: A Prospective Analysis of 1056 FNA Samples

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Mechanism of 3-nitropropionic acid-induced membrane permeability transition of isolated mitochondria and its suppression by L-carnitine

rs58542926 variant in TM6SF2 is a point mutation, wherein the Guanine nucleotide gets converted into adenine nucleotide in exon 6 (GA)

Iron supplementation should be initiated as soon as possible, because the cardiomyopathy may be driven solely by iron deficiency A complete iron evaluation should include: Ferritin Serum iron TIBC Transferrin saturation CBC Reticulocyte count when needed C-reactive protein, because inflammation can alter ferritin interpretation In gluten-sensitive patients, iron deficiency is a common problem