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Plos One
|
October 19, 2017
Perception of climate change in patients with chronic lung disease
Jeremias Götschke, Pontus Mertsch, Michael Bischof, et al.
Nature Medicine
|
March 27, 2012
Commensal bacteria-derived signals regulate basophil hematopoiesis and allergic inflammation
David A Hill, Mark C Siracusa, Michael C Abt, et al.
European Journal of Immunology
|
August 29, 2025
Signal Transducer and Activator of Transcription 3 (STAT3) Variant p.K709N Causes Hyper-IgE Syndrome Likely by Impaired STAT3-Dimer Formation
Beate Hagl, Benedikt D Spielberger, Betina Neumann, et al.
Immunotherapy
|
July 29, 2024
A patient empowerment program for primary immunodeficiency improves quality of life in children and adolescents
Maria Fasshauer, Gesine Schuermann, Norbert Gebert, et al.
Allergy
|
February 23, 2019
Lung disease in STAT3 hyper-IgE syndrome requires intense therapy
Carolin Kröner, Jens Neumann, Julia Ley-Zaporozhan, et al.
The Journal of Allergy and Clinical Immunology
|
August 18, 2009
Comèl-Netherton syndrome defined as primary immunodeficiency
Ellen D Renner, Dominik Hartl, Stacey Rylaarsdam, et al.
Pediatric Hematology and Oncology
|
August 18, 2012
Clinical and immunological correction of DOCK8 deficiency by allogeneic hematopoietic stem cell transplantation following a reduced toxicity conditioning regimen
Heidrun Boztug, Cäcilia Karitnig-Weiß, Bernd Ausserer, et al.
Journal of the American Society of Nephrology : JASN
|
February 11, 2014
Stat3 programs Th17-specific regulatory T cells to control GN
Malte A Kluger, Michael Luig, Claudia Wegscheid, et al.
Journal of Clinical Immunology
|
April 16, 2013
Lung parenchyma surgery in autosomal dominant hyper-IgE syndrome
Alexandra F Freeman, Ellen D Renner, Carolyn Henderson, et al.
Scientific Reports
|
November 15, 2018
Somatic alterations compromised molecular diagnosis of DOCK8 hyper-IgE syndrome caused by a novel intronic splice site mutation
Beate Hagl, Benedikt D Spielberger, Silvia Thoene, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 35) with videos related to
Sort By:
Page
of 4
Plos One
|
October 19, 2017
Perception of climate change in patients with chronic lung disease
Jeremias Götschke, Pontus Mertsch, Michael Bischof, et al.
Nature Medicine
|
March 27, 2012
Commensal bacteria-derived signals regulate basophil hematopoiesis and allergic inflammation
David A Hill, Mark C Siracusa, Michael C Abt, et al.
European Journal of Immunology
|
August 29, 2025
Signal Transducer and Activator of Transcription 3 (STAT3) Variant p.K709N Causes Hyper-IgE Syndrome Likely by Impaired STAT3-Dimer Formation
Beate Hagl, Benedikt D Spielberger, Betina Neumann, et al.
Immunotherapy
|
July 29, 2024
A patient empowerment program for primary immunodeficiency improves quality of life in children and adolescents
Maria Fasshauer, Gesine Schuermann, Norbert Gebert, et al.
Allergy
|
February 23, 2019
Lung disease in STAT3 hyper-IgE syndrome requires intense therapy
Carolin Kröner, Jens Neumann, Julia Ley-Zaporozhan, et al.
The Journal of Allergy and Clinical Immunology
|
August 18, 2009
Comèl-Netherton syndrome defined as primary immunodeficiency
Ellen D Renner, Dominik Hartl, Stacey Rylaarsdam, et al.
Pediatric Hematology and Oncology
|
August 18, 2012
Clinical and immunological correction of DOCK8 deficiency by allogeneic hematopoietic stem cell transplantation following a reduced toxicity conditioning regimen
Heidrun Boztug, Cäcilia Karitnig-Weiß, Bernd Ausserer, et al.
Journal of the American Society of Nephrology : JASN
|
February 11, 2014
Stat3 programs Th17-specific regulatory T cells to control GN
Malte A Kluger, Michael Luig, Claudia Wegscheid, et al.
Journal of Clinical Immunology
|
April 16, 2013
Lung parenchyma surgery in autosomal dominant hyper-IgE syndrome
Alexandra F Freeman, Ellen D Renner, Carolyn Henderson, et al.
Scientific Reports
|
November 15, 2018
Somatic alterations compromised molecular diagnosis of DOCK8 hyper-IgE syndrome caused by a novel intronic splice site mutation
Beate Hagl, Benedikt D Spielberger, Silvia Thoene, et al.
Page
of 4