Showing results (11-20 of 23) with videos related to
Sort By:
Pageof 3
Journal of the American Heart Association|November 9, 2017
Impaired Central Pulsatile Hemodynamics in Children and Adolescents With Marfan SyndromeAndrea Grillo, Paolo Salvi, Susan Marelli, et al.Drug Metabolism and Personalized Therapy|July 31, 2016
Pharmacogenetic approach to losartan in Marfan patients: a starting point to improve dosing regimen?Felicia Stefania Falvella, Susan Marelli, Stefania Cheli, et al.Journal of Child Neurology|September 30, 2016
Clinical Characterization, Genetics, and Long-Term Follow-up of a Large Cohort of Patients With Agenesis of the Corpus CallosumRomina Romaniello, Susan Marelli, Roberto Giorda, et al.Journal of Hypertension|December 7, 2017
Aortic dilatation in Marfan syndrome: role of arterial stiffness and fibrillin-1 variantsPaolo Salvi, Andrea Grillo, Susan Marelli, et al.Brain Sciences|January 21, 2022
SCN2A Pathogenic Variants and Epilepsy: Heterogeneous Clinical, Genetic and Diagnostic FeaturesRoberta Epifanio, Roberto Giorda, Maria Carolina Merlano, et al.Journal of the American Heart Association|April 26, 2019
Unreliable Estimation of Aortic Pulse Wave Velocity Provided by the Mobil-O-Graph Algorithm-Based System in Marfan SyndromePaolo Salvi, Giulia Furlanis, Andrea Grillo, et al.Frontiers in Genetics|December 18, 2018
Segmental Maternal UPD of Chromosome 7q in a Patient With Pendred and Silver Russell Syndromes-Like FeaturesValentina Cirello, Valentina Giorgini, Chiara Castronovo, et al.Neuropediatrics|June 21, 2023
A Novel De novo Heterozygous Mutation in the SON Gene Associated with Septo-optic Dysplasia: A New PhenotypeLudovica Pasca, Davide Politano, Anna Cavallini, et al.European Journal of Human Genetics : EJHG|July 22, 2010
Genotype-phenotype relationship in three cases with overlapping 19p13.12 microdeletionsMaria C Bonaglia, Susan Marelli, Francesca Novara, et al.European Journal of Human Genetics : EJHG|July 24, 2008
Detailed phenotype-genotype study in five patients with chromosome 6q16 deletion: narrowing the critical region for Prader-Willi-like phenotypeMaria Clara Bonaglia, Roberto Ciccone, Giorgio Gimelli, et al.Pageof 3