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Publications by Ivana Zavaroni
Characterization of Three Kindreds With Familial Combined Hypolipidemia Caused by Loss-Of-Function Mutations of ANGPTL3
Circulation: Cardiovascular Genetics
Hyperinsulinemia and Impaired Leptin-Adiponectin Ratio Associate With Endothelial Nitric Oxide Synthase Polymorphisms in Subjects With In-Stent Restenosis
American Journal of Physiology - Endocrinology and Metabolism
Endocrinology
Physiology
Metabolism
Diabetes
Related publications
Prevalence of ANGPTL3 and APOB Gene Mutations in Subjects With Combined Hypolipidemia
Arteriosclerosis, Thrombosis, and Vascular Biology
Cardiovascular Medicine
Cardiology
Studies on Three Kindreds With Familial Hypercholesterolemia and Xanthomatosis; Genetic, Clinical and Pathogenic Aspects
The Journal of Japan Atherosclerosis Society
Molecular Characterization of Loss-Of-Function Mutations in PCSK9 and Identification of a Compound Heterozygote
American Journal of Human Genetics
Genetics
Loss of Function Mutations inNNTAre Associated With Left Ventricular NoncompactionCLINICAL PERSPECTIVE
Circulation: Cardiovascular Genetics
Malformations in the Murine Kidney Caused by Loss of CENP-F Function
Anatomical Record
Evolution
Ecology
Systematics
Anatomy
Histology
Behavior
Biotechnology
Novel PITX2c Loss-Of-Function Mutations Associated With Complex Congenital Heart Disease
International Journal of Molecular Medicine
Medicine
Genetics
Novel PTPRQ Mutations Identified in Three Congenital Hearing Loss Patients With Various Types of Hearing Loss
Annals of Otology, Rhinology and Laryngology
Medicine
Otorhinolaryngology
Effects of MYBPC3 Loss of Function Mutations Preceding Hypertrophic Cardiomyopathy
JCI insight
Medicine
Molecular Pathology of Familial Hypertrophic Cardiomyopathy Caused by Mutations in the Cardiac Myosin Binding Protein C Gene.
Journal of Medical Genetics
Genetics
