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Publications by Elisa Pinotti
Prevalence of ANGPTL3 and APOB Gene Mutations in Subjects With Combined Hypolipidemia
Arteriosclerosis, Thrombosis, and Vascular Biology
Cardiovascular Medicine
Cardiology
Related publications
Characterization of Three Kindreds With Familial Combined Hypolipidemia Caused by Loss-Of-Function Mutations of ANGPTL3
Circulation: Cardiovascular Genetics
Frequency of ApoB and ApoE Gene Mutations as Causes of Hypobetalipoproteinemia in the Framingham Offspring Population
Arteriosclerosis, Thrombosis, and Vascular Biology
Cardiovascular Medicine
Cardiology
Dysbetalipoproteinemia in a Kindred With Hypobetalipoproteinemia Due to Mutations in the Genes for ApoB (ApoB-70.5) and ApoE (ApoE2)
Arteriosclerosis and Thrombosis: A Journal of Vascular Biology
Predictors and Prevalence of Paraganglioma Syndrome Associated With Mutations of the SDHC Gene
JAMA - Journal of the American Medical Association
Medicine
Mutations in RAD21 Disrupt Regulation of APOB in Patients With Chronic Intestinal Pseudo-Obstruction
Gastroenterology
Hepatology
Gastroenterology
Sources and Properties of Triglyceride-Rich Lipoproteins Containing apoB-48 and apoB-100 in Postprandial Blood Plasma of Patients With Primary Combined Hyperlipidemia
Journal of Lipid Research
Biochemistry
Endocrinology
Cell Biology
Selenium Supplementation Fails to Correct the Selenoprotein Synthesis Defect in Subjects With SBP2 Gene Mutations
Thyroid
Medicine
Endocrinology
Metabolism
Diabetes
DISCOVERY: A Study Examining the Prevalence of Transthyretin Mutations in Subjects Suspected of Having Cardiac Amyloidosis
Orphanet Journal of Rare Diseases
Medicine
Genetics
Pharmacology
Increased Oxidative Stress Markers in Cerebrospinal Fluid From Healthy Subjects With Parkinson’s Disease-Associated LRRK2 Gene Mutations
Frontiers in Aging Neuroscience
Aging
Cognitive Neuroscience
