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Barbara Lombardo

Showing results (31-40 of 57) with videos related to

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International Journal of Molecular Sciences|November 23, 2017
Fast Detection of a BRCA2 Large Genomic Duplication by Next Generation Sequencing as a Single Procedure: A Case ReportMarcella Nunziato, Flavio Starnone, Barbara Lombardo, et al.
Gene Therapy|February 1, 2019
Helper-dependent adenovirus-mediated gene transfer of a secreted LDL receptor/transferrin chimeric protein reduces aortic atherosclerosis in LDL receptor-deficient miceEleonora Leggiero, Giuseppe Labruna, Laura Iaffaldano, et al.
Gene|December 10, 2013
Microduplications in 22q11.2 and 8q22.1 associated with mild mental retardation and generalized overgrowthMarina Tarsitano, Carlo Ceglia, Antonio Novelli, et al.
Antibiotics (Basel, Switzerland)|April 25, 2020
Human Defensins: A Novel Approach in the Fight against Skin Colonizing <i>Staphylococcus</i> a<i>ureus</i>Olga Scudiero, Mariarita Brancaccio, Cristina Mennitti, et al.
Clinical Chemistry and Laboratory Medicine|June 13, 2019
Molecular diagnosis of MODY3 permitted to reveal a de novo 12q24.31 deletion and to explain a complex phenotype in a young diabetic patientFernanda Iafusco, Paola De Sanctis, Daniele Pirozzi, et al.
Heliyon|December 10, 2024
Effect of elite sport activity on salivary microbiota: The case of water poloIolanda Veneruso, Cristina Mennitti, Alessandro Gentile, et al.
Frontiers in Psychiatry|November 29, 2023
Positive effects of physical activity in autism spectrum disorder: how influences behavior, metabolic disorder and gut microbiotaAnnaluisa Ranieri, Cristina Mennitti, Noemi Falcone, et al.
Journal of Clinical Medicine|August 13, 2020
Athlete's Passport: Prevention of Infections, Inflammations, Injuries and Cardiovascular DiseasesCristina Mennitti, Mariarita Brancaccio, Luca Gentile, et al.
American Journal of Medical Genetics. Part A|June 4, 2016
Mulibrey nanism: Two novel mutations in a child identified by Array CGH and DNA sequencingEnza Mozzillo, Carla Cozzolino, Rita Genesio, et al.
Frontiers in Oncology|March 15, 2021
Case Report: Detection of a Novel Germline <i>PALB2</i> Deletion in a Young Woman With Hereditary Breast Cancer: When the Patient's Phenotype History Doesn't LieCarmine De Angelis, Carmela Nardelli, Paola Concolino, et al.
Pageof 6

Showing results (31-40 of 57) with videos related to

Sort By:
Pageof 6
International Journal of Molecular Sciences|November 23, 2017
Fast Detection of a BRCA2 Large Genomic Duplication by Next Generation Sequencing as a Single Procedure: A Case ReportMarcella Nunziato, Flavio Starnone, Barbara Lombardo, et al.
Gene Therapy|February 1, 2019
Helper-dependent adenovirus-mediated gene transfer of a secreted LDL receptor/transferrin chimeric protein reduces aortic atherosclerosis in LDL receptor-deficient miceEleonora Leggiero, Giuseppe Labruna, Laura Iaffaldano, et al.
Gene|December 10, 2013
Microduplications in 22q11.2 and 8q22.1 associated with mild mental retardation and generalized overgrowthMarina Tarsitano, Carlo Ceglia, Antonio Novelli, et al.
Antibiotics (Basel, Switzerland)|April 25, 2020
Human Defensins: A Novel Approach in the Fight against Skin Colonizing <i>Staphylococcus</i> a<i>ureus</i>Olga Scudiero, Mariarita Brancaccio, Cristina Mennitti, et al.
Clinical Chemistry and Laboratory Medicine|June 13, 2019
Molecular diagnosis of MODY3 permitted to reveal a de novo 12q24.31 deletion and to explain a complex phenotype in a young diabetic patientFernanda Iafusco, Paola De Sanctis, Daniele Pirozzi, et al.
Heliyon|December 10, 2024
Effect of elite sport activity on salivary microbiota: The case of water poloIolanda Veneruso, Cristina Mennitti, Alessandro Gentile, et al.
Frontiers in Psychiatry|November 29, 2023
Positive effects of physical activity in autism spectrum disorder: how influences behavior, metabolic disorder and gut microbiotaAnnaluisa Ranieri, Cristina Mennitti, Noemi Falcone, et al.
Journal of Clinical Medicine|August 13, 2020
Athlete's Passport: Prevention of Infections, Inflammations, Injuries and Cardiovascular DiseasesCristina Mennitti, Mariarita Brancaccio, Luca Gentile, et al.
American Journal of Medical Genetics. Part A|June 4, 2016
Mulibrey nanism: Two novel mutations in a child identified by Array CGH and DNA sequencingEnza Mozzillo, Carla Cozzolino, Rita Genesio, et al.
Frontiers in Oncology|March 15, 2021
Case Report: Detection of a Novel Germline <i>PALB2</i> Deletion in a Young Woman With Hereditary Breast Cancer: When the Patient's Phenotype History Doesn't LieCarmine De Angelis, Carmela Nardelli, Paola Concolino, et al.
Pageof 6