A MUC13 Variant Enhances Intestinal Ferric Iron Absorption in Unexplained Hyperferritinemia
ABSTRACT Background & Aims Hyperferritinemia frequently remains unexplained despite comprehensive evaluation. We conducted a sequencing‐based exome association study to identify genetic variants associated with plasma ferritin levels in patients with unexplained hyperferritinemia.
Jonas Callet +22 more
wiley +1 more source
Testing for myocardial ischemia in patients presenting with sustained monomorphic Ventricular Tachycardia(VT) even without evidence of acute myocardial infarction is a tempting strategy that is frequently utilized in clinical practice.
Sideris, Skevos +13 more
core +1 more source
Kaposi's Varicelliform Eruption in a Child with Atopic Dermatitis: A Case Report. [PDF]
Lendínez-Jurado A +2 more
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Asymptomatic Tattoo-Associated Cutaneous Nontuberculous Mycobacterial Infection: Case Report. [PDF]
Alihosseini C +5 more
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Howard-James C, Shudell E.
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Sustained monomorphic ventricular tachycardia as the first manifestation of probable cardiac sarcoidosis: A case report. [PDF]
Sanusi M +13 more
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Sustained Ventricular Tachycardia as the First Presentation of Hereditary Transthyretin Amyloidosis With the Glu109Gln Mutation. [PDF]
Weiss T +4 more
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Au-Yang W +4 more
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Post-TAVR Bundle Branch Re-entrant Ventricular Tachycardia Managed Without ICD: A Rare Turn of Rhythm. [PDF]
Desai H, Chahal CAA, Obeng-Gyimah EK.
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<i>NKX2-5</i> mutation in a family with ventricular tachycardia and aborted sudden cardiac death. [PDF]
Pandey A, Bromberg B, Menon D.
europepmc +1 more source

