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Vera Gallo

Showing results (1-10 of 38) 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|January 18, 2014
FOXN1 in organ development and human diseasesLoredana Palamaro, Rosa Romano, Anna Fusco, 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|July 23, 2013
FOXN1: A Master Regulator Gene of Thymic Epithelial Development ProgramRosa Romano, Loredana Palamaro, Anna Fusco, 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.
International Reviews of Immunology|January 19, 2012
Severe combined immunodeficiences: new and old scenariosGiuseppina Aloj, Giuliana Giardino, Leopoldo Valentino, et al.
American Journal of Medical Genetics. Part A|September 13, 2018
Otolaryngological features in a cohort of patients affected with 22q11.2 deletion syndrome: A monocentric surveyFiorentino Grasso, Emilia Cirillo, Giuseppe Quaremba, et al.
Annals of the New York Academy of Sciences|August 4, 2015
Severe combined immunodeficiency--an updateEmilia Cirillo, Giuliana Giardino, Vera Gallo, et al.
International Reviews of Immunology|October 23, 2012
Genetic basis of altered central tolerance and autoimmune diseases: a lesson from AIRE mutationsDonatella Capalbo, Giuliana Giardino, Lucia De Martino, et al.
Expert Review of Clinical Immunology|December 22, 2012
Alterations of the autoimmune regulator transcription factor and failure of central tolerance: APECED as a modelVera Gallo, Giuliana Giardino, Donatella Capalbo, et al.
Pageof 4

Showing results (1-10 of 38) with videos related to

Sort By:
Pageof 4
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|January 18, 2014
FOXN1 in organ development and human diseasesLoredana Palamaro, Rosa Romano, Anna Fusco, 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|July 23, 2013
FOXN1: A Master Regulator Gene of Thymic Epithelial Development ProgramRosa Romano, Loredana Palamaro, Anna Fusco, 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.
International Reviews of Immunology|January 19, 2012
Severe combined immunodeficiences: new and old scenariosGiuseppina Aloj, Giuliana Giardino, Leopoldo Valentino, et al.
American Journal of Medical Genetics. Part A|September 13, 2018
Otolaryngological features in a cohort of patients affected with 22q11.2 deletion syndrome: A monocentric surveyFiorentino Grasso, Emilia Cirillo, Giuseppe Quaremba, et al.
Annals of the New York Academy of Sciences|August 4, 2015
Severe combined immunodeficiency--an updateEmilia Cirillo, Giuliana Giardino, Vera Gallo, et al.
International Reviews of Immunology|October 23, 2012
Genetic basis of altered central tolerance and autoimmune diseases: a lesson from AIRE mutationsDonatella Capalbo, Giuliana Giardino, Lucia De Martino, et al.
Expert Review of Clinical Immunology|December 22, 2012
Alterations of the autoimmune regulator transcription factor and failure of central tolerance: APECED as a modelVera Gallo, Giuliana Giardino, Donatella Capalbo, et al.
Pageof 4