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Circulation|February 6, 2002
Insulin causes endothelial dysfunction in humans: sites and mechanismsGuido Arcaro, Anna Cretti, Sara Balzano, et al.
Molecular Vision|April 28, 2021
Heterozygous deletions of noncoding parts of the <i>PRPF31</i> gene cause retinitis pigmentosa via reduced gene expressionFrancesco Paolo Ruberto, Sara Balzano, Prasanthi Namburi, et al.
Diabetes Therapy : Research, Treatment and Education of Diabetes and Related Disorders|September 22, 2018
Clinical Impact of 5 Years of Liraglutide Treatment on Cardiovascular Risk Factors in Patients with Type 2 Diabetes Mellitus in a Real-Life Setting in Italy: An Observational StudyVera Frison, Natalino Simioni, Alberto Marangoni, et al.
Molecular Cytogenetics|July 16, 2015
Short stature and primary ovarian insufficiency possibly due to chromosomal position effect in a balanced X;1 translocationRita Genesio, Angela Mormile, Maria Rosaria Licenziati, et al.
Cardiovascular Drugs and Therapy|July 15, 2025
Real-World Efficacy of Inclisiran in Veneto Region (Italy): The INCLIVEN Multicenter RegistryFrancesco Briani, Elena Sani, Gabriele Venturi, et al.
Clinical Therapeutics|January 29, 2015
Correlation between baseline characteristics and clinical outcomes in a large population of diabetes patients treated with liraglutide in a real-world setting in ItalyAnnunziata Lapolla, Vera Frison, Michela Bettio, et al.
American Journal of Human Genetics|September 3, 2016
Mutations in CEP78 Cause Cone-Rod Dystrophy and Hearing Loss Associated with Primary-Cilia DefectsKonstantinos Nikopoulos, Pietro Farinelli, Basilio Giangreco, et al.
Nature|February 11, 2021
Non-coding deletions identify Maenli lncRNA as a limb-specific En1 regulatorLila Allou, Sara Balzano, Andreas Magg, et al.
Human Molecular Genetics|February 8, 2017
Mutations in the polyglutamylase gene TTLL5, expressed in photoreceptor cells and spermatozoa, are associated with cone-rod degeneration and reduced male fertilityNicola Bedoni, Lonneke Haer-Wigman, Veronika Vaclavik, et al.
Nature Genetics|May 24, 2016
NANS-mediated synthesis of sialic acid is required for brain and skeletal developmentClara D M van Karnebeek, Luisa Bonafé, Xiao-Yan Wen, et al.
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