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Maria D'Apolito

Showing results (21-30 of 71) with videos related to

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Turk Pediatri Arsivi|February 28, 2018
Vascular toxicity of urea, a new "old player" in the pathogenesis of chronic renal failure induced cardiovascular diseasesIda Giardino, Maria D'Apolito, Michael Brownlee, et al.
World Journal of Pediatrics : WJP|December 20, 2015
Genetic analysis of Italian patients with congenital tufting enteropathyMaria d'Apolito, Daniela Pisanelli, Flavio Faletra, et al.
Foods (Basel, Switzerland)|November 25, 2023
Ancient Grain Flours with Different Degrees of Sifting: Advances in Knowledge of Nutritional, Technological, and Microbiological AspectsTiziana Di Renzo, Giovanni Cascone, Giuseppina Crescente, et al.
Cancer Immunology, Immunotherapy : CII|September 28, 2004
Rituximab induces different but overlapping sets of genes in human B-lymphoma cell linesElena Cittera, Chiara Onofri, Maria D'Apolito, et al.
Genes|February 25, 2023
A Novel DLG1 Variant in a Family with Brugada Syndrome: Clinical Characteristics and In Silico AnalysisMaria d'Apolito, Francesco Santoro, Rosa Santacroce, et al.
The Journal of Clinical Endocrinology and Metabolism|January 14, 2016
HMGB1 Is Increased by CFTR Loss of Function, Is Lowered by Insulin, and Increases In Vivo at Onset of CFRDLuisa Montanini, Francesca Cirillo, Arianna Smerieri, et al.
International Journal of Molecular Sciences|February 13, 2025
Genetic Background and Clinical Phenotype in an Italian Cohort with Inherited Arrhythmia Syndromes and Arrhythmogenic Cardiomyopathy (ACM): A Whole-Exome Sequencing StudyMaria d'Apolito, Francesco Santoro, Alessandra Ranaldi, et al.
Atherosclerosis|June 23, 2017
Urea-induced ROS accelerate senescence in endothelial progenitor cellsMaria D'Apolito, Anna Laura Colia, Maria Lasalvia, et al.
Human Mutation|February 16, 2005
Spectrum of UGT1A1 mutations in Crigler-Najjar (CN) syndrome patients: identification of twelve novel alleles and genotype-phenotype correlationVeronica Servedio, Maria d'Apolito, Nunzia Maiorano, et al.
Pacing and Clinical Electrophysiology : PACE|February 24, 2026
Unmasking Brugada ECG Pattern in Myotonic Dystrophy Type 2 With an ANK2 VariantMaria d'Apolito, Maria Rosaria D'Apice, Francesco Santoro, et al.
Pageof 8

Showing results (21-30 of 71) with videos related to

Sort By:
Pageof 8
Turk Pediatri Arsivi|February 28, 2018
Vascular toxicity of urea, a new "old player" in the pathogenesis of chronic renal failure induced cardiovascular diseasesIda Giardino, Maria D'Apolito, Michael Brownlee, et al.
World Journal of Pediatrics : WJP|December 20, 2015
Genetic analysis of Italian patients with congenital tufting enteropathyMaria d'Apolito, Daniela Pisanelli, Flavio Faletra, et al.
Foods (Basel, Switzerland)|November 25, 2023
Ancient Grain Flours with Different Degrees of Sifting: Advances in Knowledge of Nutritional, Technological, and Microbiological AspectsTiziana Di Renzo, Giovanni Cascone, Giuseppina Crescente, et al.
Cancer Immunology, Immunotherapy : CII|September 28, 2004
Rituximab induces different but overlapping sets of genes in human B-lymphoma cell linesElena Cittera, Chiara Onofri, Maria D'Apolito, et al.
Genes|February 25, 2023
A Novel DLG1 Variant in a Family with Brugada Syndrome: Clinical Characteristics and In Silico AnalysisMaria d'Apolito, Francesco Santoro, Rosa Santacroce, et al.
The Journal of Clinical Endocrinology and Metabolism|January 14, 2016
HMGB1 Is Increased by CFTR Loss of Function, Is Lowered by Insulin, and Increases In Vivo at Onset of CFRDLuisa Montanini, Francesca Cirillo, Arianna Smerieri, et al.
International Journal of Molecular Sciences|February 13, 2025
Genetic Background and Clinical Phenotype in an Italian Cohort with Inherited Arrhythmia Syndromes and Arrhythmogenic Cardiomyopathy (ACM): A Whole-Exome Sequencing StudyMaria d'Apolito, Francesco Santoro, Alessandra Ranaldi, et al.
Atherosclerosis|June 23, 2017
Urea-induced ROS accelerate senescence in endothelial progenitor cellsMaria D'Apolito, Anna Laura Colia, Maria Lasalvia, et al.
Human Mutation|February 16, 2005
Spectrum of UGT1A1 mutations in Crigler-Najjar (CN) syndrome patients: identification of twelve novel alleles and genotype-phenotype correlationVeronica Servedio, Maria d'Apolito, Nunzia Maiorano, et al.
Pacing and Clinical Electrophysiology : PACE|February 24, 2026
Unmasking Brugada ECG Pattern in Myotonic Dystrophy Type 2 With an ANK2 VariantMaria d'Apolito, Maria Rosaria D'Apice, Francesco Santoro, et al.
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