List of works by Tali Stauber

A Large Cohort of RAG1/2-Deficient SCID Patients-Clinical, Immunological, and Prognostic Analysis

scientific article published on 14 December 2019

Atypical immune phenotype in severe combined immunodeficiency patients with novel mutations in IL2RG and JAK3

scientific article published on 14 September 2020

CD137 deficiency causes immune dysregulation with predisposition to lymphomagenesis

scientific article published on 01 October 2019

Co-appearance of OPV and BCG vaccine-derived complications in two infants with severe combined immunodeficiency

scientific article published on 01 June 2018

Combined immunodeficiency in a patient with mosaic monosomy 21.

scientific article published on 24 May 2016

Correction to: Novel Mutations in RASGRP1 Are Associated with Immunodeficiency, Immune Dysregulation, and EBV-Induced Lymphoma

scientific article published on 01 August 2018

First Year of Israeli Newborn Screening for Severe Combined Immunodeficiency-Clinical Achievements and Insights

scientific article published on 6 November 2017

Immune reconstitution after HSCT in SCID-a cohort of conditioned and unconditioned patients

scientific article published on 01 June 2019

Inherited SLP76 deficiency in humans causes severe combined immunodeficiency, neutrophil and platelet defects

scientific article published on 01 March 2021

Late diagnosis of Chronic Granulomatous Disease

scientific article published on 07 June 2020

MHC II deficient infant identified by newborn screening program for SCID

scientific article published on 01 August 2018

Novel MALT1 Mutation Linked to Immunodeficiency, Immune Dysregulation, and an Abnormal T Cell Receptor Repertoire

scientific article published on 29 April 2019

Novel Mutations in RASGRP1 are Associated with Immunodeficiency, Immune Dysregulation, and EBV-Induced Lymphoma

scientific article published on 20 July 2018

Reduced Function and Diversity of T Cell Repertoire and Distinct Clinical Course in Patients With IL7RA Mutation

scientific article published on 17 July 2019

Whole exome sequencing (WES) approach for diagnosing primary immunodeficiencies (PIDs) in a highly consanguineous community

scientific article published on 03 March 2020

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