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Vaccine
|
November 1, 2024
Vaccinations in children of non-European origin: The Vax4globe survey
Viviana Moschese, Simona Graziani, Antonietta Spadea, et al.
Eclinicalmedicine
|
June 23, 2025
Long-term outcome in Wiskott-Aldrich syndrome and X-linked thrombocytopenia patients: an observational -prospective multi-center study of the Italian Primary Immune Deficiency Network (IPINET)
Annarosa Soresina, Roberto Rondelli, Lucia Dora Notarangelo, et al.
Clinical Immunology (Orlando, Fla.)
|
September 10, 2002
Clinical, immunological, and molecular analysis in a large cohort of patients with X-linked agammaglobulinemia: an Italian multicenter study
Alessandro Plebani, Annarosa Soresina, Roberto Rondelli, et al.
The Journal of Pediatrics
|
March 25, 2014
Clinical features and follow-up in patients with 22q11.2 deletion syndrome
Caterina Cancrini, Pamela Puliafito, Maria Cristina Digilio, et al.
Journal of Clinical Immunology
|
April 21, 2022
The Impact of SARS-CoV-2 Infection in Patients with Inborn Errors of Immunity: the Experience of the Italian Primary Immunodeficiencies Network (IPINet)
Giuliana Giardino, Cinzia Milito, Vassilios Lougaris, et al.
The Journal of Allergy and Clinical Immunology. in Practice
|
March 30, 2019
Immunophenotype Anomalies Predict the Development of Autoimmune Cytopenia in 22q11.2 Deletion Syndrome
Davide Montin, Agostina Marolda, Francesco Licciardi, et al.
The Journal of Allergy and Clinical Immunology
|
August 23, 2020
Consensus of the Italian Primary Immunodeficiency Network on transition management from pediatric to adult care in patients affected with childhood-onset inborn errors of immunity
Emilia Cirillo, Giuliana Giardino, Silvia Ricci, et al.
Journal of Human Immunity
|
December 5, 2025
Inborn errors of immunity: Manifestation, treatment, and outcome-an ESID registry 1994-2024 report on 30,628 patients
Gerhard Kindle, Mickaël Alligon, Michael H Albert, et al.
Journal of Clinical Immunology
|
January 19, 2021
Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
Giuliana Giardino, Svetlana O Sharapova, Peter Ciznar, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 26, 2025
Inborn errors of immunity: manifestation, treatment, and outcome - an ESID registry 1994-2024 report on 30,628 patients
Gerhard Kindle, Mickaël Alligon, Michael H Albert, et al.
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of 15
Search research articles
Search
Showing results (121-130 of 149) with videos related to
Sort By:
Page
of 15
Vaccine
|
November 1, 2024
Vaccinations in children of non-European origin: The Vax4globe survey
Viviana Moschese, Simona Graziani, Antonietta Spadea, et al.
Eclinicalmedicine
|
June 23, 2025
Long-term outcome in Wiskott-Aldrich syndrome and X-linked thrombocytopenia patients: an observational -prospective multi-center study of the Italian Primary Immune Deficiency Network (IPINET)
Annarosa Soresina, Roberto Rondelli, Lucia Dora Notarangelo, et al.
Clinical Immunology (Orlando, Fla.)
|
September 10, 2002
Clinical, immunological, and molecular analysis in a large cohort of patients with X-linked agammaglobulinemia: an Italian multicenter study
Alessandro Plebani, Annarosa Soresina, Roberto Rondelli, et al.
The Journal of Pediatrics
|
March 25, 2014
Clinical features and follow-up in patients with 22q11.2 deletion syndrome
Caterina Cancrini, Pamela Puliafito, Maria Cristina Digilio, et al.
Journal of Clinical Immunology
|
April 21, 2022
The Impact of SARS-CoV-2 Infection in Patients with Inborn Errors of Immunity: the Experience of the Italian Primary Immunodeficiencies Network (IPINet)
Giuliana Giardino, Cinzia Milito, Vassilios Lougaris, et al.
The Journal of Allergy and Clinical Immunology. in Practice
|
March 30, 2019
Immunophenotype Anomalies Predict the Development of Autoimmune Cytopenia in 22q11.2 Deletion Syndrome
Davide Montin, Agostina Marolda, Francesco Licciardi, et al.
The Journal of Allergy and Clinical Immunology
|
August 23, 2020
Consensus of the Italian Primary Immunodeficiency Network on transition management from pediatric to adult care in patients affected with childhood-onset inborn errors of immunity
Emilia Cirillo, Giuliana Giardino, Silvia Ricci, et al.
Journal of Human Immunity
|
December 5, 2025
Inborn errors of immunity: Manifestation, treatment, and outcome-an ESID registry 1994-2024 report on 30,628 patients
Gerhard Kindle, Mickaël Alligon, Michael H Albert, et al.
Journal of Clinical Immunology
|
January 19, 2021
Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
Giuliana Giardino, Svetlana O Sharapova, Peter Ciznar, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 26, 2025
Inborn errors of immunity: manifestation, treatment, and outcome - an ESID registry 1994-2024 report on 30,628 patients
Gerhard Kindle, Mickaël Alligon, Michael H Albert, et al.
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of 15