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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 diseases
Ida Giardino, Maria D'Apolito, Michael Brownlee, et al.
World Journal of Pediatrics : WJP
|
December 20, 2015
Genetic analysis of Italian patients with congenital tufting enteropathy
Maria 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 Aspects
Tiziana 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 lines
Elena 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 Analysis
Maria 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 CFRD
Luisa 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 Study
Maria d'Apolito, Francesco Santoro, Alessandra Ranaldi, et al.
Atherosclerosis
|
June 23, 2017
Urea-induced ROS accelerate senescence in endothelial progenitor cells
Maria 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 correlation
Veronica 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 Variant
Maria d'Apolito, Maria Rosaria D'Apice, Francesco Santoro, et al.
Page
of 8
Search research articles
Search
Showing results (21-30 of 71) with videos related to
Sort By:
Page
of 8
Turk Pediatri Arsivi
|
February 28, 2018
Vascular toxicity of urea, a new "old player" in the pathogenesis of chronic renal failure induced cardiovascular diseases
Ida Giardino, Maria D'Apolito, Michael Brownlee, et al.
World Journal of Pediatrics : WJP
|
December 20, 2015
Genetic analysis of Italian patients with congenital tufting enteropathy
Maria 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 Aspects
Tiziana 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 lines
Elena 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 Analysis
Maria 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 CFRD
Luisa 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 Study
Maria d'Apolito, Francesco Santoro, Alessandra Ranaldi, et al.
Atherosclerosis
|
June 23, 2017
Urea-induced ROS accelerate senescence in endothelial progenitor cells
Maria 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 correlation
Veronica 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 Variant
Maria d'Apolito, Maria Rosaria D'Apice, Francesco Santoro, et al.
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of 8