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Raffaele Badolato

Showing results (141-150 of 183) with videos related to

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The Journal of Allergy and Clinical Immunology. in Practice|February 5, 2019
Long-Term Outcome of WHIM Syndrome in 18 Patients: High Risk of Lung Disease and HPV-Related MalignanciesLaura Dotta, Lucia Dora Notarangelo, Daniele Moratto, et al.
The Journal of Allergy and Clinical Immunology|February 5, 2013
Combined DOCK8 and CLEC7A mutations causing immunodeficiency in 3 brothers with diarrhea, eczema, and infectionsDarrell L Dinwiddie, Stephen F Kingsmore, Sonia Caracciolo, et al.
Blood|March 31, 2012
Exome sequencing reveals a pallidin mutation in a Hermansky-Pudlak-like primary immunodeficiency syndromeRaffaele Badolato, Alberto Prandini, Sonia Caracciolo, et al.
Children (Basel, Switzerland)|June 28, 2023
Longitudinal Characterization of Immune Response in a Cohort of Children Hospitalized with Multisystem Inflammatory SyndromeLaura Dotta, Daniele Moratto, Marco Cattalini, et al.
Italian Journal of Pediatrics|February 13, 2024
Increased bronchiolitis burden and severity after the pandemic: a national multicentric studySergio Ghirardo, Nicola Ullmann, Alessandro Zago, et al.
Journal of Clinical Immunology|May 27, 2019
Clinical and Laboratory Features of 184 Italian Pediatric Patients Affected with Selective IgA Deficiency (SIgAD): a Longitudinal Single-Center StudyVassilios Lougaris, Annamaria Sorlini, Chiara Monfredini, et al.
Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin|May 14, 2020
Multicentre Italian study of SARS-CoV-2 infection in children and adolescents, preliminary data as at 10 April 2020Silvia Garazzino, Carlotta Montagnani, Daniele Donà, et al.
JCI Insight|March 8, 2023
Reduced G protein signaling despite impaired internalization and β-arrestin recruitment in patients carrying a CXCR4Leu317fsX3 mutation causing WHIM syndromeRajesh Kumar, Samantha Milanesi, Martyna Szpakowska, et al.
Italian Journal of Pediatrics|November 29, 2025
Invasive Group A Streptococcus infections in children during the post-pandemic period: results from a multicenter study in ItalyElena Chiappini, Marco Renni, Maia De Luca, et al.
Frontiers in Immunology|May 3, 2021
Case Report: Hypomorphic Function and Somatic Reversion in DOCK8 Deficiency in One Patient With Two Novel Variants and Sclerosing CholangitisFrancesco Saettini, Grazia Fazio, Daniele Moratto, et al.
Pageof 19

Showing results (141-150 of 183) with videos related to

Sort By:
Pageof 19
The Journal of Allergy and Clinical Immunology. in Practice|February 5, 2019
Long-Term Outcome of WHIM Syndrome in 18 Patients: High Risk of Lung Disease and HPV-Related MalignanciesLaura Dotta, Lucia Dora Notarangelo, Daniele Moratto, et al.
The Journal of Allergy and Clinical Immunology|February 5, 2013
Combined DOCK8 and CLEC7A mutations causing immunodeficiency in 3 brothers with diarrhea, eczema, and infectionsDarrell L Dinwiddie, Stephen F Kingsmore, Sonia Caracciolo, et al.
Blood|March 31, 2012
Exome sequencing reveals a pallidin mutation in a Hermansky-Pudlak-like primary immunodeficiency syndromeRaffaele Badolato, Alberto Prandini, Sonia Caracciolo, et al.
Children (Basel, Switzerland)|June 28, 2023
Longitudinal Characterization of Immune Response in a Cohort of Children Hospitalized with Multisystem Inflammatory SyndromeLaura Dotta, Daniele Moratto, Marco Cattalini, et al.
Italian Journal of Pediatrics|February 13, 2024
Increased bronchiolitis burden and severity after the pandemic: a national multicentric studySergio Ghirardo, Nicola Ullmann, Alessandro Zago, et al.
Journal of Clinical Immunology|May 27, 2019
Clinical and Laboratory Features of 184 Italian Pediatric Patients Affected with Selective IgA Deficiency (SIgAD): a Longitudinal Single-Center StudyVassilios Lougaris, Annamaria Sorlini, Chiara Monfredini, et al.
Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin|May 14, 2020
Multicentre Italian study of SARS-CoV-2 infection in children and adolescents, preliminary data as at 10 April 2020Silvia Garazzino, Carlotta Montagnani, Daniele Donà, et al.
JCI Insight|March 8, 2023
Reduced G protein signaling despite impaired internalization and β-arrestin recruitment in patients carrying a CXCR4Leu317fsX3 mutation causing WHIM syndromeRajesh Kumar, Samantha Milanesi, Martyna Szpakowska, et al.
Italian Journal of Pediatrics|November 29, 2025
Invasive Group A Streptococcus infections in children during the post-pandemic period: results from a multicenter study in ItalyElena Chiappini, Marco Renni, Maia De Luca, et al.
Frontiers in Immunology|May 3, 2021
Case Report: Hypomorphic Function and Somatic Reversion in DOCK8 Deficiency in One Patient With Two Novel Variants and Sclerosing CholangitisFrancesco Saettini, Grazia Fazio, Daniele Moratto, et al.
Pageof 19