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Journal of Clinical Immunology
|
September 26, 2022
Lymphoma as an Exclusion Criteria for CVID Diagnosis Revisited
Vincent Allain, Virginie Grandin, Véronique Meignin, et al.
The Journal of Clinical Investigation
|
December 7, 2018
Loss of ARHGEF1 causes a human primary antibody deficiency
Amine Bouafia, Sébastien Lofek, Julie Bruneau, et al.
Journal of Clinical Immunology
|
February 23, 2020
Correction to: Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee
Stuart G Tangye, Waleed Al-Herz, Aziz Bousfiha, et al.
Journal of Clinical Immunology
|
January 19, 2020
Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee
Stuart G Tangye, Waleed Al-Herz, Aziz Bousfiha, et al.
Blood
|
October 29, 2021
Abatacept is useful in autoimmune cytopenia with immunopathologic manifestations caused by CTLA-4 defects
C Dhunputh, S Ducassou, H Fernandes, et al.
Blood
|
October 28, 2010
First use of thymus transplantation therapy for FOXN1 deficiency (nude/SCID): a report of 2 cases
M Louise Markert, José G Marques, Bénédicte Neven, et al.
The Journal of Clinical Investigation
|
February 23, 2012
Partial MCM4 deficiency in patients with growth retardation, adrenal insufficiency, and natural killer cell deficiency
Laure Gineau, Céline Cognet, Nihan Kara, et al.
The Journal of Allergy and Clinical Immunology
|
March 3, 2017
Lack of interaction between NEMO and SHARPIN impairs linear ubiquitination and NF-κB activation and leads to incontinentia pigmenti
Elodie Bal, Emmanuel Laplantine, Yamina Hamel, et al.
The Journal of Experimental Medicine
|
April 29, 2015
Inherited IL-17RC deficiency in patients with chronic mucocutaneous candidiasis
Yun Ling, Sophie Cypowyj, Caner Aytekin, et al.
Haematologica
|
April 22, 2017
Mutations in the adaptor-binding domain and associated linker region of p110δ cause Activated PI3K-δ Syndrome 1 (APDS1)
Lucie Heurtier, Hicham Lamrini, Loïc Chentout, et al.
Page
of 40
Search research articles
Search
Showing results (211-220 of 400) with videos related to
Sort By:
Page
of 40
Journal of Clinical Immunology
|
September 26, 2022
Lymphoma as an Exclusion Criteria for CVID Diagnosis Revisited
Vincent Allain, Virginie Grandin, Véronique Meignin, et al.
The Journal of Clinical Investigation
|
December 7, 2018
Loss of ARHGEF1 causes a human primary antibody deficiency
Amine Bouafia, Sébastien Lofek, Julie Bruneau, et al.
Journal of Clinical Immunology
|
February 23, 2020
Correction to: Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee
Stuart G Tangye, Waleed Al-Herz, Aziz Bousfiha, et al.
Journal of Clinical Immunology
|
January 19, 2020
Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee
Stuart G Tangye, Waleed Al-Herz, Aziz Bousfiha, et al.
Blood
|
October 29, 2021
Abatacept is useful in autoimmune cytopenia with immunopathologic manifestations caused by CTLA-4 defects
C Dhunputh, S Ducassou, H Fernandes, et al.
Blood
|
October 28, 2010
First use of thymus transplantation therapy for FOXN1 deficiency (nude/SCID): a report of 2 cases
M Louise Markert, José G Marques, Bénédicte Neven, et al.
The Journal of Clinical Investigation
|
February 23, 2012
Partial MCM4 deficiency in patients with growth retardation, adrenal insufficiency, and natural killer cell deficiency
Laure Gineau, Céline Cognet, Nihan Kara, et al.
The Journal of Allergy and Clinical Immunology
|
March 3, 2017
Lack of interaction between NEMO and SHARPIN impairs linear ubiquitination and NF-κB activation and leads to incontinentia pigmenti
Elodie Bal, Emmanuel Laplantine, Yamina Hamel, et al.
The Journal of Experimental Medicine
|
April 29, 2015
Inherited IL-17RC deficiency in patients with chronic mucocutaneous candidiasis
Yun Ling, Sophie Cypowyj, Caner Aytekin, et al.
Haematologica
|
April 22, 2017
Mutations in the adaptor-binding domain and associated linker region of p110δ cause Activated PI3K-δ Syndrome 1 (APDS1)
Lucie Heurtier, Hicham Lamrini, Loïc Chentout, et al.
Page
of 40