Publications by authors named "Andrea Micaloni"

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Novel ACTA1 mutation causes late-presenting nemaline myopathy with unusual dark cores.
Matteo Garibaldi, Fabiana Fattori, Elena Maria Pennisi, Gioia Merlonghi, Laura Fionda, Andrea Micaloni

Neuromuscul Disord· February 2021

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Pharmacological restoration of autophagy reduces hypertension-related stroke occurrence.
Maurizio Forte, Franca Bianchi, Maria Cotugno, Simona Marchitti, Elena De Falco, Andrea Micaloni

Autophagy· August 2020

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The reduction of NDUFC2 expression is associated with mitochondrial impairment in circulating mononuclear cells of patients with acute coronary syndrome.
Salvatore Raffa, Xiao Lan Diana Chin, Rosita Stanzione, Maurizio Forte, Franca Bianchi, Andrea Micaloni

Int J Cardiol· July 2019

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Chronic heart failure is characterized by altered mitochondrial function and structure in circulating leucocytes.
Roberta Coluccia, Salvatore Raffa, Danilo Ranieri, Andrea Micaloni, Sabatino Valente

Oncotarget· October 2018

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In vitro characterization of mitochondrial function and structure in rat and human cells with a deficiency of the NADH: ubiquinone oxidoreductase Ndufc2 subunit.
Salvatore Raffa, Cristina Scrofani, Sabatino Valente, Andrea Micaloni, Maurizio Forte

Hum Mol Genet· December 2017

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