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Maria d'Apolito

Showing results (1-10 of 63) with videos related to

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Turk Pediatri Arsivi|February 28, 2018
Levels of inflammatory cytokines from peripheral blood mononuclear cells of children with cow's milk protein allergyMaria D'Apolito, Angelo Campanozzi, Ida Giardino, et al.
Handbook of Clinical Neurology|February 21, 2023
Lessons from immunotherapies in multiple sclerosisMarianna G Rispoli, Maria D'Apolito, Valeria Pozzilli, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|October 2, 2019
Hereditary angioedema: Looking for bradykinin production and triggers of vascular permeabilityMaurizio Margaglione, Maria D'Apolito, Rosa Santocroce, et al.
Gene|April 12, 2002
Cloning of the murine non-muscle myosin heavy chain IIA gene ortholog of human MYH9 responsible for May-Hegglin, Sebastian, Fechtner, and Epstein syndromesMaria D'Apolito, Vito Guarnieri, Marianna Boncristiano, et al.
Journal of Clinical Medicine|June 2, 2021
The Genetics of Hereditary Angioedema: A ReviewRosa Santacroce, Giovanna D'Andrea, Angela Bruna Maffione, et al.
Blood|September 15, 2005
Microcytic anemia and hepatic iron overload in a child with compound heterozygous mutations in DMT1 (SCL11A2)Achille Iolascon, Maria d'Apolito, Veronica Servedio, et al.
Haematologica|January 19, 2007
Seven novel mutations of the UGT1A1 gene in patients with unconjugated hyperbilirubinemiaMaria D'Apolito, Agnese Marrone, Veronica Servedio, et al.
Biology of the Neonate|June 1, 2006
Kernicterus associated with hereditary spherocytosis and UGT1A1 promoter polymorphismAlberto Berardi, Licia Lugli, Fabrizio Ferrari, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|January 29, 2019
Angiopoietin-1 haploinsufficiency affects the endothelial barrier and causes hereditary angioedemaMaria d'Apolito, Rosa Santacroce, Anna Laura Colia, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 22, 2021
Status migrainosus: a potential adverse reaction to Comirnaty (BNT162b2, BioNtech/Pfizer) COVID-19 vaccine-a case reportStefano Consoli, Fedele Dono, Giacomo Evangelista, et al.
Pageof 7

Showing results (1-10 of 63) with videos related to

Sort By:
Pageof 7
Turk Pediatri Arsivi|February 28, 2018
Levels of inflammatory cytokines from peripheral blood mononuclear cells of children with cow's milk protein allergyMaria D'Apolito, Angelo Campanozzi, Ida Giardino, et al.
Handbook of Clinical Neurology|February 21, 2023
Lessons from immunotherapies in multiple sclerosisMarianna G Rispoli, Maria D'Apolito, Valeria Pozzilli, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|October 2, 2019
Hereditary angioedema: Looking for bradykinin production and triggers of vascular permeabilityMaurizio Margaglione, Maria D'Apolito, Rosa Santocroce, et al.
Gene|April 12, 2002
Cloning of the murine non-muscle myosin heavy chain IIA gene ortholog of human MYH9 responsible for May-Hegglin, Sebastian, Fechtner, and Epstein syndromesMaria D'Apolito, Vito Guarnieri, Marianna Boncristiano, et al.
Journal of Clinical Medicine|June 2, 2021
The Genetics of Hereditary Angioedema: A ReviewRosa Santacroce, Giovanna D'Andrea, Angela Bruna Maffione, et al.
Blood|September 15, 2005
Microcytic anemia and hepatic iron overload in a child with compound heterozygous mutations in DMT1 (SCL11A2)Achille Iolascon, Maria d'Apolito, Veronica Servedio, et al.
Haematologica|January 19, 2007
Seven novel mutations of the UGT1A1 gene in patients with unconjugated hyperbilirubinemiaMaria D'Apolito, Agnese Marrone, Veronica Servedio, et al.
Biology of the Neonate|June 1, 2006
Kernicterus associated with hereditary spherocytosis and UGT1A1 promoter polymorphismAlberto Berardi, Licia Lugli, Fabrizio Ferrari, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|January 29, 2019
Angiopoietin-1 haploinsufficiency affects the endothelial barrier and causes hereditary angioedemaMaria d'Apolito, Rosa Santacroce, Anna Laura Colia, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 22, 2021
Status migrainosus: a potential adverse reaction to Comirnaty (BNT162b2, BioNtech/Pfizer) COVID-19 vaccine-a case reportStefano Consoli, Fedele Dono, Giacomo Evangelista, et al.
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