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Journal of Lipid Research|February 22, 2005
Denaturing high-performance liquid chromatography in the detection of ABCA1 gene mutations in familial HDL deficiencyTommaso Fasano, Letizia Bocchi, Livia Pisciotta, et al.
Clinical Biochemistry|May 7, 2026
Direct serum biomarkers of liver fibrosis in metabolic dysfunction-associated steatotic liver disease: A scoping reviewValentina Pecoraro, Fabio Nascimbeni, Filippo Gabrielli, et al.
Atherosclerosis. Supplements|October 3, 2017
The study of familial hypercholesterolemia in Italy: A narrative reviewStefano Bertolini, Livia Pisciotta, Tommaso Fasano, et al.
Atherosclerosis|December 17, 2008
Degradation of LDLR protein mediated by 'gain of function' PCSK9 mutants in normal and ARH cellsTommaso Fasano, Xi-Ming Sun, Dilipkumar D Patel, et al.
Atherosclerosis|October 24, 2007
A novel mutation of the apolipoprotein A-I gene in a family with familial combined hyperlipidemiaLivia Pisciotta, Tommaso Fasano, Laura Calabresi, et al.
Thrombosis Research|January 26, 2022
Four cases of acquired hemophilia A following immunization with mRNA BNT162b2 SARS-CoV-2 vaccineMaria Cristina Leone, Simone Canovi, Annalisa Pilia, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 23, 2010
Multiple abnormally spliced ABCA1 mRNAs caused by a novel splice site mutation of ABCA1 gene in a patient with Tangier diseaseLetizia Bocchi, Livia Pisciotta, Tommaso Fasano, et al.
The Laryngoscope|February 23, 2017
Laboratory assessment of sudden sensorineural hearing loss: A case-control studyTommaso Fasano, Thelma A Pertinhez, Lorenzo Tribi, et al.
Journal of Clinical Lipidology|September 28, 2017
Incidental finding of severe hypertriglyceridemia in children. Role of multiple rare variants in genes affecting plasma triglyceridePaola Sabrina Buonuomo, Claudio Rabacchi, Marina Macchiaiolo, et al.
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