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Merja Helminen

Showing results (51-60 of 59) with videos related to

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Plos One|October 17, 2015
IL-10 Gene Polymorphisms Are Associated with Post-Bronchiolitis Lung Function Abnormalities at Six Years of AgeEero Lauhkonen, Petri Koponen, Johanna Teräsjärvi, et al.
Acta Paediatrica (Oslo, Norway : 1992)|July 31, 2021
Multi-inflammatory syndrome and Kawasaki disease in children during the COVID-19 pandemic: A nationwide register-based study and time series analysisUlla Koskela, Otto Helve, Emmi Sarvikivi, et al.
Acta Paediatrica (Oslo, Norway : 1992)|March 19, 2024
Pneumonia, wheezing and asthma were more common in children after thymectomy due to open-heart surgeryRea Rantanen, Minna Honkila, Hanna-Riikka Kämä, et al.
European Journal of Immunology|December 3, 2014
Dysregulation of adaptive immune responses in complement C3-deficient patientsPirkka T Pekkarinen, Nelli Heikkilä, Kai Kisand, et al.
Antioxidants & Redox Signaling|May 3, 2014
Reactive oxygen species deficiency induces autoimmunity with type 1 interferon signatureTiina Kelkka, Deborah Kienhöfer, Markus Hoffmann, et al.
The Journal of Allergy and Clinical Immunology|January 25, 2017
Damaging heterozygous mutations in NFKB1 lead to diverse immunologic phenotypesMeri Kaustio, Emma Haapaniemi, Helka Göös, et al.
The New England Journal of Medicine|June 18, 2015
Inherited DOCK2 Deficiency in Patients with Early-Onset Invasive InfectionsKerry Dobbs, Cecilia Domínguez Conde, Shen-Ying Zhang, et al.
The Journal of Allergy and Clinical Immunology|April 11, 2017
Outcome of hematopoietic cell transplantation for DNA double-strand break repair disordersJames Slack, Michael H Albert, Dmitry Balashov, et al.
The Journal of Allergy and Clinical Immunology|April 13, 2020
Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutationsTiziana Lorenzini, Manfred Fliegauf, Nils Klammer, et al.
Pageof 6

Showing results (51-60 of 59) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 59 results.
Plos One|October 17, 2015
IL-10 Gene Polymorphisms Are Associated with Post-Bronchiolitis Lung Function Abnormalities at Six Years of AgeEero Lauhkonen, Petri Koponen, Johanna Teräsjärvi, et al.
Acta Paediatrica (Oslo, Norway : 1992)|July 31, 2021
Multi-inflammatory syndrome and Kawasaki disease in children during the COVID-19 pandemic: A nationwide register-based study and time series analysisUlla Koskela, Otto Helve, Emmi Sarvikivi, et al.
Acta Paediatrica (Oslo, Norway : 1992)|March 19, 2024
Pneumonia, wheezing and asthma were more common in children after thymectomy due to open-heart surgeryRea Rantanen, Minna Honkila, Hanna-Riikka Kämä, et al.
European Journal of Immunology|December 3, 2014
Dysregulation of adaptive immune responses in complement C3-deficient patientsPirkka T Pekkarinen, Nelli Heikkilä, Kai Kisand, et al.
Antioxidants & Redox Signaling|May 3, 2014
Reactive oxygen species deficiency induces autoimmunity with type 1 interferon signatureTiina Kelkka, Deborah Kienhöfer, Markus Hoffmann, et al.
The Journal of Allergy and Clinical Immunology|January 25, 2017
Damaging heterozygous mutations in NFKB1 lead to diverse immunologic phenotypesMeri Kaustio, Emma Haapaniemi, Helka Göös, et al.
The New England Journal of Medicine|June 18, 2015
Inherited DOCK2 Deficiency in Patients with Early-Onset Invasive InfectionsKerry Dobbs, Cecilia Domínguez Conde, Shen-Ying Zhang, et al.
The Journal of Allergy and Clinical Immunology|April 11, 2017
Outcome of hematopoietic cell transplantation for DNA double-strand break repair disordersJames Slack, Michael H Albert, Dmitry Balashov, et al.
The Journal of Allergy and Clinical Immunology|April 13, 2020
Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutationsTiziana Lorenzini, Manfred Fliegauf, Nils Klammer, et al.
Pageof 6