Search Results - "Cardiero, G."

Pathogenicity classification of variants associated with familial hypercholesterolemia: Comparison between guidelines by Di Taranto, M.D., Ferrandino, M., Cardiero, G., Gianfico, C., Flagiello, C., Fortunato, G.

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lncRNAs signature of human carotid atherosclerotic plaques: Differences between high- and low-grade lesions by Veneruso, I., D'Argenio, V., Di Taranto, M.D., Cardiero, G., Bracale, U., Salvatore, F., Fortunato, G.

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A novel missense variant in CREB3L3 gene associated with severe hypertriglyceridemia by Cardiero, G., Palma, D., Di Taranto, M.D., Esposito, M.V., Iannuzzo, G., Di Minno, M.N.D., Molino, C., Iannuzzi, A., Fortunato, G.

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Identification of a rare variants in ABCG5/ABCG8 genes in patients with clinical suspect of familial hyperchoelsterolemia by Giacobbe, C., Di Taranto, M.D., Palma, D., Gelzo, M., Caputo, M., Cardiero, G., Corso, G., Guardamagna, O., Fortunato, G.

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Evidence of novel APO B gene complex allele causing familial hypercholesterolaemia by Palma, D., Cardiero, G., Flagiello, C., Galicia-Garcia, U., Larrea, A., Di Taranto, M.D., Martin, C., Iannuzzo, G., Di Minno, M.N.D., Pipolo, A., Fortunato, G.

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Spectrum of genetic variants in patients suffering from familial chylomicronaemia syndrome and multifactorial chylomicronaemia syndrome by Giacobbe, C., Di Taranto, M.D., Palma, D., Maione, G., Cardiero, G., Forte, F., Iannuzzo, G., Rubba, P., Fortunato, G.

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In vitro characterization revealed five new potential pathogenic variants in the APOB gene by Di Taranto, M.D., Galicia, U., Larrea, A., Giacobbe, C., Calcaterra, I., Palma, D., Cardiero, G., Iannuzzo, G., Di Minno, M.N.D., Iannuzzi, A., Martín, C., Fortunato, G.

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Genetics and biochemical profile of patients with homozygous familial hypercholesterolemia by Di Taranto, M.D., Giacobbe, C., Buonaiuto, A., Calcaterra, I., Palma, D., Maione, G., Cardiero, G., Iannuzzo, G., Di Minno, M.N.D., Rubba, P., Fortunato, G.

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