Search research articles
Contact Us
Filters
Showing results (151-160 of 183) with videos related to
Page
of 19
Sort By:
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.
Science Immunology
|
September 17, 2021
Combined immunodeficiency with autoimmunity caused by a homozygous missense mutation in inhibitor of nuclear factor š¯›‹B kinase alpha (IKKĪ±)
Wayne Bainter, Vassilios Lougaris, Jacqueline G Wallace, 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.
Nature Immunology
|
May 15, 2012
DOCK8 functions as an adaptor that links TLR-MyD88 signaling to B cell activation
Haifa H Jabara, Douglas R McDonald, Erin Janssen, et al.
Nature Communications
|
March 14, 2019
Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly
Najim Lahrouchi, Aman George, Ilham Ratbi, et al.
Cell Reports
|
March 5, 2020
The Interplay between CD27<sup>dull</sup> and CD27<sup>bright</sup> B Cells Ensures the Flexibility, Stability, and Resilience of Human B Cell Memory
Ola Grimsholm, Eva Piano Mortari, Alexey N Davydov, et al.
American Journal of Human Genetics
|
May 22, 2012
Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity
Gabriela Lopez-Herrera, Giacomo Tampella, Qiang Pan-Hammarstrƶm, et al.
Frontiers in Immunology
|
August 29, 2019
Clinical, Immunological, and Molecular Features of Typical and Atypical Severe Combined Immunodeficiency: Report of the Italian Primary Immunodeficiency Network
Emilia Cirillo, Caterina Cancrini, Chiara Azzari, et al.
Science (New York, N.Y.)
|
April 13, 2013
Ribosomal protein SA haploinsufficiency in humans with isolated congenital asplenia
Alexandre Bolze, Nizar Mahlaoui, Minji Byun, et al.
Page
of 19
Search research articles
Search
Showing results (151-160 of 183) with videos related to
Sort By:
Page
of 19
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.
Science Immunology
|
September 17, 2021
Combined immunodeficiency with autoimmunity caused by a homozygous missense mutation in inhibitor of nuclear factor š¯›‹B kinase alpha (IKKĪ±)
Wayne Bainter, Vassilios Lougaris, Jacqueline G Wallace, 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.
Nature Immunology
|
May 15, 2012
DOCK8 functions as an adaptor that links TLR-MyD88 signaling to B cell activation
Haifa H Jabara, Douglas R McDonald, Erin Janssen, et al.
Nature Communications
|
March 14, 2019
Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly
Najim Lahrouchi, Aman George, Ilham Ratbi, et al.
Cell Reports
|
March 5, 2020
The Interplay between CD27<sup>dull</sup> and CD27<sup>bright</sup> B Cells Ensures the Flexibility, Stability, and Resilience of Human B Cell Memory
Ola Grimsholm, Eva Piano Mortari, Alexey N Davydov, et al.
American Journal of Human Genetics
|
May 22, 2012
Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity
Gabriela Lopez-Herrera, Giacomo Tampella, Qiang Pan-Hammarstrƶm, et al.
Frontiers in Immunology
|
August 29, 2019
Clinical, Immunological, and Molecular Features of Typical and Atypical Severe Combined Immunodeficiency: Report of the Italian Primary Immunodeficiency Network
Emilia Cirillo, Caterina Cancrini, Chiara Azzari, et al.
Science (New York, N.Y.)
|
April 13, 2013
Ribosomal protein SA haploinsufficiency in humans with isolated congenital asplenia
Alexandre Bolze, Nizar Mahlaoui, Minji Byun, et al.
Page
of 19