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Janine Reichenbach

Showing results (51-60 of 65) with videos related to

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The Journal of Clinical Investigation|October 3, 2003
A hypermorphic IkappaBalpha mutation is associated with autosomal dominant anhidrotic ectodermal dysplasia and T cell immunodeficiencyGilles Courtois, Asma Smahi, Janine Reichenbach, 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 syndromeEllen D Renner, Stacey Rylaarsdam, Stephanie Anover-Sombke, et al.
The Journal of Allergy and Clinical Immunology|March 15, 2011
Quantification of κ-deleting recombination excision circles in Guthrie cards for the identification of early B-cell maturation defectsNoriko Nakagawa, Kohsuke Imai, Hirokazu Kanegane, et al.
Current Gene Therapy|May 19, 2015
Successful Combination of Sequential Gene Therapy and Rescue Allo-HSCT in Two Children with X-CGD - Importance of TimingUlrich Siler, Anna Paruzynski, Heidi Holtgreve-Grez, et al.
The Journal of Allergy and Clinical Immunology|September 7, 2010
Diagnostic approach to the hyper-IgE syndromes: immunologic and clinical key findings to differentiate hyper-IgE syndromes from atopic dermatitisLena F Schimke, Julie Sawalle-Belohradsky, Joachim Roesler, et al.
Journal of Clinical Immunology|March 7, 2019
Human DOCK2 Deficiency: Report of a Novel Mutation and Evidence for Neutrophil DysfunctionLeen Moens, Mieke Gouwy, Barbara Bosch, et al.
The Journal of Allergy and Clinical Immunology|May 25, 2012
Clinical, molecular, and cellular immunologic findings in patients with SP110-associated veno-occlusive disease with immunodeficiency syndromeSimon T Cliffe, Donald B Bloch, Santi Suryani, et al.
The Journal of Pediatrics|July 25, 2009
Identification of severe combined immunodeficiency by T-cell receptor excision circles quantification using neonatal guthrie cardsYoichi Morinishi, Kohsuke Imai, Noriko Nakagawa, et al.
Blood|April 27, 2016
Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotypeJulie Toubiana, Satoshi Okada, Julia Hiller, et al.
The Journal of Allergy and Clinical Immunology|May 26, 2016
Clinical and immunologic phenotype associated with activated phosphoinositide 3-kinase δ syndrome 2: A cohort studyElodie Elkaim, Benedicte Neven, Julie Bruneau, et al.
Pageof 7

Showing results (51-60 of 65) with videos related to

Sort By:
Pageof 7
The Journal of Clinical Investigation|October 3, 2003
A hypermorphic IkappaBalpha mutation is associated with autosomal dominant anhidrotic ectodermal dysplasia and T cell immunodeficiencyGilles Courtois, Asma Smahi, Janine Reichenbach, 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 syndromeEllen D Renner, Stacey Rylaarsdam, Stephanie Anover-Sombke, et al.
The Journal of Allergy and Clinical Immunology|March 15, 2011
Quantification of κ-deleting recombination excision circles in Guthrie cards for the identification of early B-cell maturation defectsNoriko Nakagawa, Kohsuke Imai, Hirokazu Kanegane, et al.
Current Gene Therapy|May 19, 2015
Successful Combination of Sequential Gene Therapy and Rescue Allo-HSCT in Two Children with X-CGD - Importance of TimingUlrich Siler, Anna Paruzynski, Heidi Holtgreve-Grez, et al.
The Journal of Allergy and Clinical Immunology|September 7, 2010
Diagnostic approach to the hyper-IgE syndromes: immunologic and clinical key findings to differentiate hyper-IgE syndromes from atopic dermatitisLena F Schimke, Julie Sawalle-Belohradsky, Joachim Roesler, et al.
Journal of Clinical Immunology|March 7, 2019
Human DOCK2 Deficiency: Report of a Novel Mutation and Evidence for Neutrophil DysfunctionLeen Moens, Mieke Gouwy, Barbara Bosch, et al.
The Journal of Allergy and Clinical Immunology|May 25, 2012
Clinical, molecular, and cellular immunologic findings in patients with SP110-associated veno-occlusive disease with immunodeficiency syndromeSimon T Cliffe, Donald B Bloch, Santi Suryani, et al.
The Journal of Pediatrics|July 25, 2009
Identification of severe combined immunodeficiency by T-cell receptor excision circles quantification using neonatal guthrie cardsYoichi Morinishi, Kohsuke Imai, Noriko Nakagawa, et al.
Blood|April 27, 2016
Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotypeJulie Toubiana, Satoshi Okada, Julia Hiller, et al.
The Journal of Allergy and Clinical Immunology|May 26, 2016
Clinical and immunologic phenotype associated with activated phosphoinositide 3-kinase δ syndrome 2: A cohort studyElodie Elkaim, Benedicte Neven, Julie Bruneau, et al.
Pageof 7