Showing results (71-80 of 83) with videos related to
Sort By:
Pageof 9
Blood|November 22, 2014
Early-onset Evans syndrome, immunodeficiency, and premature immunosenescence associated with tripeptidyl-peptidase II deficiencyPolina Stepensky, Anne Rensing-Ehl, Ruth Gather, et al.Journal of Immunology (Baltimore, Md. : 1950)|December 23, 2011
Antiviral and regulatory T cell immunity in a patient with stromal interaction molecule 1 deficiencySebastian Fuchs, Anne Rensing-Ehl, Carsten Speckmann, et al.Proceedings of the National Academy of Sciences of the United States of America|February 9, 2011
ORAI1-mediated calcium influx is required for human cytotoxic lymphocyte degranulation and target cell lysisAndrea Maul-Pavicic, Samuel C C Chiang, Anne Rensing-Ehl, et al.Immunology and Cell Biology|May 24, 2018
CD57 identifies T cells with functional senescence before terminal differentiation and relative telomere shortening in patients with activated PI3 kinase delta syndromePaola Cura Daball, Monica Sofia Ventura Ferreira, Sandra Ammann, et al.Blood|January 9, 2016
Mutations in AP3D1 associated with immunodeficiency and seizures define a new type of Hermansky-Pudlak syndromeSandra Ammann, Ansgar Schulz, Ingeborg Krägeloh-Mann, et al.European Radiology|April 25, 2019
Patient radiation dose in percutaneous biliary interventions: recommendations for DRLs on the basis of a multicentre studyDaniel Schmitz, Thomas Vogl, Nour-Eldin Abdelrehim Nour-Eldin, et al.The Journal of Allergy and Clinical Immunology|September 24, 2016
A prospective study on the natural history of patients with profound combined immunodeficiency: An interim analysisCarsten Speckmann, Sam Doerken, Alessandro Aiuti, et al.The Journal of Allergy and Clinical Immunology|June 12, 2017
Hematopoietic stem cell transplantation in patients with gain-of-function signal transducer and activator of transcription 1 mutationsJennifer W Leiding, Satoshi Okada, David Hagin, et al.The Journal of Allergy and Clinical Immunology|November 18, 2023
Abnormal biomarkers predict complex FAS or FADD defects missed by exome sequencingAnne Rensing-Ehl, Myriam Ricarda Lorenz, Marita Führer, 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.Pageof 9