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Frontiers in Immunology
|
January 3, 2022
Establishing the Molecular Diagnoses in a Cohort of 291 Patients With Predominantly Antibody Deficiency by Targeted Next-Generation Sequencing: Experience From a Monocentric Study
Jessica Rojas-Restrepo, Andrés Caballero-Oteyza, Katrin Huebscher, et al.
Orphanet Journal of Rare Diseases
|
November 14, 2018
The burden of common variable immunodeficiency disorders: a retrospective analysis of the European Society for Immunodeficiency (ESID) registry data
Irina Odnoletkova, Gerhard Kindle, Isabella Quinti, et al.
Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz
|
February 16, 2019
Stephan Ehl, Christian Bogdan, Tim Niehues, et al.
Pediatric Blood & Cancer
|
January 6, 2021
Is neutralization of IFN-γ sufficient to control inflammation in HLH?
Stephan Ehl, Tatiana von Bahr Greenwood, Elisabet Bergsten, et al.
The Journal of Allergy and Clinical Immunology
|
April 25, 2021
Initial presenting manifestations in 16,486 patients with inborn errors of immunity include infections and noninfectious manifestations
Julian Thalhammer, Gerhard Kindle, Alexandra Nieters, et al.
Journal of Clinical Immunology
|
April 21, 2025
A Novel Description of Immunodeficiency and Immune Dysregulation in a 14-Year-Old Girl with Noonan Syndrome 13
Saira Tabassum, Sarah Grün, Ben Molloy, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
May 31, 2018
CD59 deficiency presenting as polyneuropathy and Moyamoya syndrome with endothelial abnormalities of small brain vessels
Christian Klemann, Janbernd Kirschner, Sandra Ammann, et al.
Frontiers in Pediatrics
|
January 22, 2025
SOCS1 deficiency-crossroads of autoimmunity and autoinflammation-two case reports
Kajetan Trojovsky, Maximilian Seidl, Florian Babor, et al.
Clinical Immunology (Orlando, Fla.)
|
June 9, 2026
Corrigendum to "Natural history of clinical manifestations in activated phosphoinositide 3-kinase δ syndrome (APDS): Time-to-event analyses using the European Society for Immunodeficiencies-APDS registry" [Clinical Immunology 283 (2025) 110632]
Maria Elena Maccari, Sven Kracker, Anita Chandra, et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology
|
July 11, 2026
Long-read sequencing reveals SVA insertion in AP3B1 causing Hermansky-Pudlak syndrome 2
Naomi Baba, Ahmed Elashy, Oliver Wegehaupt, et al.
Page
of 24
Search research articles
Search
Showing results (71-80 of 239) with videos related to
Sort By:
Page
of 24
Frontiers in Immunology
|
January 3, 2022
Establishing the Molecular Diagnoses in a Cohort of 291 Patients With Predominantly Antibody Deficiency by Targeted Next-Generation Sequencing: Experience From a Monocentric Study
Jessica Rojas-Restrepo, Andrés Caballero-Oteyza, Katrin Huebscher, et al.
Orphanet Journal of Rare Diseases
|
November 14, 2018
The burden of common variable immunodeficiency disorders: a retrospective analysis of the European Society for Immunodeficiency (ESID) registry data
Irina Odnoletkova, Gerhard Kindle, Isabella Quinti, et al.
Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz
|
February 16, 2019
Stephan Ehl, Christian Bogdan, Tim Niehues, et al.
Pediatric Blood & Cancer
|
January 6, 2021
Is neutralization of IFN-γ sufficient to control inflammation in HLH?
Stephan Ehl, Tatiana von Bahr Greenwood, Elisabet Bergsten, et al.
The Journal of Allergy and Clinical Immunology
|
April 25, 2021
Initial presenting manifestations in 16,486 patients with inborn errors of immunity include infections and noninfectious manifestations
Julian Thalhammer, Gerhard Kindle, Alexandra Nieters, et al.
Journal of Clinical Immunology
|
April 21, 2025
A Novel Description of Immunodeficiency and Immune Dysregulation in a 14-Year-Old Girl with Noonan Syndrome 13
Saira Tabassum, Sarah Grün, Ben Molloy, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
May 31, 2018
CD59 deficiency presenting as polyneuropathy and Moyamoya syndrome with endothelial abnormalities of small brain vessels
Christian Klemann, Janbernd Kirschner, Sandra Ammann, et al.
Frontiers in Pediatrics
|
January 22, 2025
SOCS1 deficiency-crossroads of autoimmunity and autoinflammation-two case reports
Kajetan Trojovsky, Maximilian Seidl, Florian Babor, et al.
Clinical Immunology (Orlando, Fla.)
|
June 9, 2026
Corrigendum to "Natural history of clinical manifestations in activated phosphoinositide 3-kinase δ syndrome (APDS): Time-to-event analyses using the European Society for Immunodeficiencies-APDS registry" [Clinical Immunology 283 (2025) 110632]
Maria Elena Maccari, Sven Kracker, Anita Chandra, et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology
|
July 11, 2026
Long-read sequencing reveals SVA insertion in AP3B1 causing Hermansky-Pudlak syndrome 2
Naomi Baba, Ahmed Elashy, Oliver Wegehaupt, et al.
Page
of 24