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Roberta Russo

Showing results (121-130 of 169) with videos related to

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Journal of Cardiothoracic and Vascular Anesthesia|November 6, 2024
Pulmonary Artery Pseudoaneurysm Due to Pulmonary Artery Catheter Placement: A New Minimally Invasive Approach to Solve a Life-threatening ComplicationRoberta Russo, Alessandro Calzolari, Valentina Salice, et al.
Hepatology (Baltimore, Md.)|August 3, 2007
Suppressor of cytokine signaling 3 (SOCS3) expression and hepatitis C virus-related chronic hepatitis: Insulin resistance and response to antiviral therapyMarcello Persico, Mario Capasso, Eliana Persico, et al.
Frontiers in Nutrition|August 23, 2021
Resveratrol Supported on Magnesium DiHydroxide (Resv@MDH) Represents an Oral Formulation of Resveratrol With Better Gastric Absorption and Bioavailability Respect to Pure ResveratrolRossana Giulietta Iannitti, Alessandro Floridi, Andrea Lazzarini, et al.
Journal of Clinical Pharmacology|May 14, 2011
Integration of pharmacogenetics and pharmacogenomics in drug development: implications for regulatory and medical decision making in pediatric diseasesChiara Piana, Linda Surh, Sabine Furst-Recktenwald, et al.
European Journal of Haematology|September 25, 2014
Congenital erythropoietic porphyria linked to GATA1-R216W mutation: challenges for diagnosisElena Di Pierro, Roberta Russo, Zeynep Karakas, et al.
Carcinogenesis|December 11, 2012
Replication of GWAS-identified neuroblastoma risk loci strengthens the role of BARD1 and affirms the cumulative effect of genetic variations on disease susceptibilityMario Capasso, Sharon J Diskin, Francesca Totaro, et al.
Archives of Neurology|May 16, 2007
Association of a presenilin 1 S170F mutation with a novel Alzheimer disease molecular phenotypeAlessandra Piccini, Gianluigi Zanusso, Roberta Borghi, et al.
American Journal of Hematology|November 28, 2012
Missense mutations in the ABCB6 transporter cause dominant familial pseudohyperkalemiaImmacolata Andolfo, Seth L Alper, Jean Delaunay, et al.
Cell Death & Disease|January 6, 2017
Neuronal hemoglobin affects dopaminergic cells' response to stressMarta Codrich, Maria Bertuzzi, Roberta Russo, et al.
Frontiers in Physiology|April 2, 2019
<i>PIEZO1</i> Hypomorphic Variants in Congenital Lymphatic Dysplasia Cause Shape and Hydration Alterations of Red Blood CellsImmacolata Andolfo, Gianluca De Rosa, Edoardo Errichiello, et al.
Pageof 17

Showing results (121-130 of 169) with videos related to

Sort By:
Pageof 17
Journal of Cardiothoracic and Vascular Anesthesia|November 6, 2024
Pulmonary Artery Pseudoaneurysm Due to Pulmonary Artery Catheter Placement: A New Minimally Invasive Approach to Solve a Life-threatening ComplicationRoberta Russo, Alessandro Calzolari, Valentina Salice, et al.
Hepatology (Baltimore, Md.)|August 3, 2007
Suppressor of cytokine signaling 3 (SOCS3) expression and hepatitis C virus-related chronic hepatitis: Insulin resistance and response to antiviral therapyMarcello Persico, Mario Capasso, Eliana Persico, et al.
Frontiers in Nutrition|August 23, 2021
Resveratrol Supported on Magnesium DiHydroxide (Resv@MDH) Represents an Oral Formulation of Resveratrol With Better Gastric Absorption and Bioavailability Respect to Pure ResveratrolRossana Giulietta Iannitti, Alessandro Floridi, Andrea Lazzarini, et al.
Journal of Clinical Pharmacology|May 14, 2011
Integration of pharmacogenetics and pharmacogenomics in drug development: implications for regulatory and medical decision making in pediatric diseasesChiara Piana, Linda Surh, Sabine Furst-Recktenwald, et al.
European Journal of Haematology|September 25, 2014
Congenital erythropoietic porphyria linked to GATA1-R216W mutation: challenges for diagnosisElena Di Pierro, Roberta Russo, Zeynep Karakas, et al.
Carcinogenesis|December 11, 2012
Replication of GWAS-identified neuroblastoma risk loci strengthens the role of BARD1 and affirms the cumulative effect of genetic variations on disease susceptibilityMario Capasso, Sharon J Diskin, Francesca Totaro, et al.
Archives of Neurology|May 16, 2007
Association of a presenilin 1 S170F mutation with a novel Alzheimer disease molecular phenotypeAlessandra Piccini, Gianluigi Zanusso, Roberta Borghi, et al.
American Journal of Hematology|November 28, 2012
Missense mutations in the ABCB6 transporter cause dominant familial pseudohyperkalemiaImmacolata Andolfo, Seth L Alper, Jean Delaunay, et al.
Cell Death & Disease|January 6, 2017
Neuronal hemoglobin affects dopaminergic cells' response to stressMarta Codrich, Maria Bertuzzi, Roberta Russo, et al.
Frontiers in Physiology|April 2, 2019
<i>PIEZO1</i> Hypomorphic Variants in Congenital Lymphatic Dysplasia Cause Shape and Hydration Alterations of Red Blood CellsImmacolata Andolfo, Gianluca De Rosa, Edoardo Errichiello, et al.
Pageof 17