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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.
Neurology
|
December 30, 2004
Clinical evaluation of idiopathic paroxysmal kinesigenic dyskinesia: new diagnostic criteria
M K Bruno, M Hallett, K Gwinn-Hardy, 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.
Allergy
|
June 6, 2014
Atopic dermatitis, STAT3- and DOCK8-hyper-IgE syndromes differ in IgE-based sensitization pattern
A C Boos, B Hagl, A Schlesinger, et al.
Allergy
|
April 8, 2021
Electrical impedance spectroscopy for the characterization of skin barrier in atopic dermatitis
Arturo O Rinaldi, Angelica Korsfeldt, Siobhan Ward, et al.
Science (New York, N.Y.)
|
April 3, 2025
Tissue-like multicellular development triggered by mechanical compression in archaea
Theopi Rados, Olivia S Leland, Pedro Escudeiro, et al.
Allergy
|
July 4, 2019
Impaired memory B-cell development and antibody maturation with a skewing toward IgE in patients with STAT3 hyper-IgE syndrome
Willem van de Veen, Carolin E Krätz, Craig I McKenzie, et al.
The Journal of Allergy and Clinical Immunology
|
July 8, 2008
Novel signal transducer and activator of transcription 3 (STAT3) mutations, reduced T(H)17 cell numbers, and variably defective STAT3 phosphorylation in hyper-IgE syndrome
Ellen D Renner, Stacey Rylaarsdam, Stephanie Anover-Sombke, et al.
Page
of 16
Search research articles
Search
Showing results (131-140 of 158) with videos related to
Sort By:
Page
of 16
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.
Neurology
|
December 30, 2004
Clinical evaluation of idiopathic paroxysmal kinesigenic dyskinesia: new diagnostic criteria
M K Bruno, M Hallett, K Gwinn-Hardy, 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.
Allergy
|
June 6, 2014
Atopic dermatitis, STAT3- and DOCK8-hyper-IgE syndromes differ in IgE-based sensitization pattern
A C Boos, B Hagl, A Schlesinger, et al.
Allergy
|
April 8, 2021
Electrical impedance spectroscopy for the characterization of skin barrier in atopic dermatitis
Arturo O Rinaldi, Angelica Korsfeldt, Siobhan Ward, et al.
Science (New York, N.Y.)
|
April 3, 2025
Tissue-like multicellular development triggered by mechanical compression in archaea
Theopi Rados, Olivia S Leland, Pedro Escudeiro, et al.
Allergy
|
July 4, 2019
Impaired memory B-cell development and antibody maturation with a skewing toward IgE in patients with STAT3 hyper-IgE syndrome
Willem van de Veen, Carolin E Krätz, Craig I McKenzie, et al.
The Journal of Allergy and Clinical Immunology
|
July 8, 2008
Novel signal transducer and activator of transcription 3 (STAT3) mutations, reduced T(H)17 cell numbers, and variably defective STAT3 phosphorylation in hyper-IgE syndrome
Ellen D Renner, Stacey Rylaarsdam, Stephanie Anover-Sombke, et al.
Page
of 16