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Emilia Cirillo

Showing results (1-10 of 68) with videos related to

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Journal of Clinical Immunology|September 22, 2017
FOXN1 Deficiency: from the Discovery to Novel Therapeutic ApproachesVera Gallo, Emilia Cirillo, Giuliana Giardino, et al.
International Reviews of Immunology|October 16, 2020
Complement system network in cell physiology and in human diseasesRoberta Romano, Giuliana Giardino, Emilia Cirillo, et al.
BMC Pediatrics|November 2, 2014
Cutaneous vasculitis in patients with autoimmune polyendocrine syndrome type 1: report of a case and brief review of the literatureNicola Improda, Donatella Capalbo, Emilia Cirillo, et al.
International Reviews of Immunology|March 17, 2015
Unraveling the Link Between Ectodermal Disorders and Primary ImmunodeficienciesRoberta D'Assante, Anna Fusco, Loredana Palamaro, et al.
Frontiers in Immunology|September 14, 2020
T-Cell Immunodeficiencies With Congenital Alterations of Thymic Development: Genes Implicated and Differential Immunological and Clinical FeaturesGiuliana Giardino, Carla Borzacchiello, Martina De Luca, et al.
Cellular Immunology|April 5, 2011
γ Chain transducing element: a shared pathway between endocrine and immune systemIlaria Vigliano, Anna Fusco, Loredana Palamaro, et al.
Scandinavian Journal of Gastroenterology|December 19, 2013
Gastrointestinal involvement in patients affected with 22q11.2 deletion syndromeGiuliana Giardino, Emilia Cirillo, Filomena Maio, et al.
Diabetes Research and Clinical Practice|August 20, 2011
Intergenerational anticipation of disease onset in people with multiple autoimmune syndromeGiuliana Giardino, Giuseppina Aloj, Emilia Cirillo, et al.
Cellular Immunology|August 11, 2010
Altered signaling through IL-12 receptor in children with very high serum IgE levelsAnna Fusco, Ilaria Vigliano, Loredana Palamaro, et al.
The Journal of Allergy and Clinical Immunology. in Practice|July 16, 2020
Clinical Phenotype, Immunological Abnormalities, and Genomic Findings in Patients with DiGeorge Spectrum Phenotype without 22q11.2 DeletionEmilia Cirillo, Maria Rosaria Prencipe, Giuliana Giardino, et al.
Pageof 7

Showing results (1-10 of 68) with videos related to

Sort By:
Pageof 7
Journal of Clinical Immunology|September 22, 2017
FOXN1 Deficiency: from the Discovery to Novel Therapeutic ApproachesVera Gallo, Emilia Cirillo, Giuliana Giardino, et al.
International Reviews of Immunology|October 16, 2020
Complement system network in cell physiology and in human diseasesRoberta Romano, Giuliana Giardino, Emilia Cirillo, et al.
BMC Pediatrics|November 2, 2014
Cutaneous vasculitis in patients with autoimmune polyendocrine syndrome type 1: report of a case and brief review of the literatureNicola Improda, Donatella Capalbo, Emilia Cirillo, et al.
International Reviews of Immunology|March 17, 2015
Unraveling the Link Between Ectodermal Disorders and Primary ImmunodeficienciesRoberta D'Assante, Anna Fusco, Loredana Palamaro, et al.
Frontiers in Immunology|September 14, 2020
T-Cell Immunodeficiencies With Congenital Alterations of Thymic Development: Genes Implicated and Differential Immunological and Clinical FeaturesGiuliana Giardino, Carla Borzacchiello, Martina De Luca, et al.
Cellular Immunology|April 5, 2011
γ Chain transducing element: a shared pathway between endocrine and immune systemIlaria Vigliano, Anna Fusco, Loredana Palamaro, et al.
Scandinavian Journal of Gastroenterology|December 19, 2013
Gastrointestinal involvement in patients affected with 22q11.2 deletion syndromeGiuliana Giardino, Emilia Cirillo, Filomena Maio, et al.
Diabetes Research and Clinical Practice|August 20, 2011
Intergenerational anticipation of disease onset in people with multiple autoimmune syndromeGiuliana Giardino, Giuseppina Aloj, Emilia Cirillo, et al.
Cellular Immunology|August 11, 2010
Altered signaling through IL-12 receptor in children with very high serum IgE levelsAnna Fusco, Ilaria Vigliano, Loredana Palamaro, et al.
The Journal of Allergy and Clinical Immunology. in Practice|July 16, 2020
Clinical Phenotype, Immunological Abnormalities, and Genomic Findings in Patients with DiGeorge Spectrum Phenotype without 22q11.2 DeletionEmilia Cirillo, Maria Rosaria Prencipe, Giuliana Giardino, et al.
Pageof 7