Tali Stauber
Tel Aviv, TA, Israel
Last Updated: 09/26/2026
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Found 33 publications
Combined Immunodeficiency Caused by a Novel Nonsense Mutation in LCK.
Journal: Journal of clinical immunology
Published: August 04, 2023
A horse or a zebra? Unusual manifestations of common cutaneous infections in primary immunodeficiency pediatric patients.
Journal: Frontiers in pediatrics
Published: November 20, 2022
Novel NHEJ1 pathogenic variant linked to severe combined immunodeficiency, microcephaly, and abnormal T and B cell receptor repertoires.
Journal: Frontiers in pediatrics
Published: February 24, 2022
Inherited SLP76 deficiency in humans causes severe combined immunodeficiency, neutrophil and platelet defects.
Journal: The Journal of experimental medicine
Published: May 24, 2020
An RTEL1 Mutation Links to Infantile-Onset Ulcerative Colitis and Severe Immunodeficiency.
Journal: Journal of clinical immunology
Published: May 03, 2020
Late diagnosis of chronic granulomatous disease.
Journal: Clinical and experimental immunology
Published: March 19, 2020
Underperformed and Underreported Testing for Persistent Oropharyngeal Poliovirus Infections in Primary Immune Deficient Patients-Risk for Reemergence of Polioviruses.
Journal: Journal of the Pediatric Infectious Diseases Society
Published: January 26, 2020
Genotype and functional correlates of disease phenotype in deficiency of adenosine deaminase 2 (DADA2).
Journal: The Journal of allergy and clinical immunology
Published: October 30, 2019
Whole exome sequencing (WES) approach for diagnosing primary immunodeficiencies (PIDs) in a highly consanguineous community.
Journal: Clinical immunology (Orlando, Fla.)
Published: October 06, 2019
Immune reconstitution after HSCT in SCID-a cohort of conditioned and unconditioned patients.
Journal: Immunologic research
Published: June 22, 2019
Last Updated: 09/26/2026