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Natalie Frede

Showing results (21-30 of 30) with videos related to

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American Journal of Human Genetics|August 18, 2015
Haploinsufficiency of the NF-κB1 Subunit p50 in Common Variable ImmunodeficiencyManfred Fliegauf, Vanessa L Bryant, Natalie Frede, et al.
The Journal of Experimental Medicine|July 28, 2017
A biallelic mutation in <i>IL6ST</i> encoding the GP130 co-receptor causes immunodeficiency and craniosynostosisTobias Schwerd, Stephen R F Twigg, Dominik Aschenbrenner, et al.
The Journal of Allergy and Clinical Immunology|December 3, 2016
Vedolizumab as a successful treatment of CTLA-4-associated autoimmune enterocolitisAlexander A Navarini, Petr Hruz, Christoph T Berger, et al.
Nature Medicine|October 21, 2014
Autosomal dominant immune dysregulation syndrome in humans with CTLA4 mutationsDesirée Schubert, Claudia Bode, Rupert Kenefeck, et al.
Journal of Clinical Immunology|November 26, 2015
The Extended Clinical Phenotype of 26 Patients with Chronic Mucocutaneous Candidiasis due to Gain-of-Function Mutations in STAT1Mark Depner, Sebastian Fuchs, Jan Raabe, et al.
Journal of Clinical Immunology|August 14, 2021
Genetic Analysis of a Cohort of 275 Patients with Hyper-IgE Syndromes and/or Chronic Mucocutaneous CandidiasisNatalie Frede, Jessica Rojas-Restrepo, Andrés Caballero Garcia de Oteyza, et al.
Inflammatory Bowel Diseases|September 21, 2017
Targeted Gene Panel Sequencing for Early-onset Inflammatory Bowel Disease and Chronic DiarrheaBritt-Sabina Petersen, Dietrich August, Renate Abt, et al.
Science Immunology|October 8, 2021
The expansion of human T-bet<sup>high</sup>CD21<sup>low</sup> B cells is T cell dependentBaerbel Keller, Valentina Strohmeier, Ina Harder, et al.
The Journal of Allergy and Clinical Immunology|May 7, 2018
Phenotype, penetrance, and treatment of 133 cytotoxic T-lymphocyte antigen 4-insufficient subjectsCharlotte Schwab, Annemarie Gabrysch, Peter Olbrich, 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 3

Showing results (21-30 of 30) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 30 results.
American Journal of Human Genetics|August 18, 2015
Haploinsufficiency of the NF-κB1 Subunit p50 in Common Variable ImmunodeficiencyManfred Fliegauf, Vanessa L Bryant, Natalie Frede, et al.
The Journal of Experimental Medicine|July 28, 2017
A biallelic mutation in <i>IL6ST</i> encoding the GP130 co-receptor causes immunodeficiency and craniosynostosisTobias Schwerd, Stephen R F Twigg, Dominik Aschenbrenner, et al.
The Journal of Allergy and Clinical Immunology|December 3, 2016
Vedolizumab as a successful treatment of CTLA-4-associated autoimmune enterocolitisAlexander A Navarini, Petr Hruz, Christoph T Berger, et al.
Nature Medicine|October 21, 2014
Autosomal dominant immune dysregulation syndrome in humans with CTLA4 mutationsDesirée Schubert, Claudia Bode, Rupert Kenefeck, et al.
Journal of Clinical Immunology|November 26, 2015
The Extended Clinical Phenotype of 26 Patients with Chronic Mucocutaneous Candidiasis due to Gain-of-Function Mutations in STAT1Mark Depner, Sebastian Fuchs, Jan Raabe, et al.
Journal of Clinical Immunology|August 14, 2021
Genetic Analysis of a Cohort of 275 Patients with Hyper-IgE Syndromes and/or Chronic Mucocutaneous CandidiasisNatalie Frede, Jessica Rojas-Restrepo, Andrés Caballero Garcia de Oteyza, et al.
Inflammatory Bowel Diseases|September 21, 2017
Targeted Gene Panel Sequencing for Early-onset Inflammatory Bowel Disease and Chronic DiarrheaBritt-Sabina Petersen, Dietrich August, Renate Abt, et al.
Science Immunology|October 8, 2021
The expansion of human T-bet<sup>high</sup>CD21<sup>low</sup> B cells is T cell dependentBaerbel Keller, Valentina Strohmeier, Ina Harder, et al.
The Journal of Allergy and Clinical Immunology|May 7, 2018
Phenotype, penetrance, and treatment of 133 cytotoxic T-lymphocyte antigen 4-insufficient subjectsCharlotte Schwab, Annemarie Gabrysch, Peter Olbrich, 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 3