Yael D. Schejter
Jerusalem, JM, Israel
Last Updated: 09/26/2026
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Found 10 publications
Biallelic Loss of Function Variants in SENP7 Cause Immunodeficiency with Neurologic and Muscular Phenotypes.
Journal: The Journal of pediatrics
Published: March 08, 2024
Successful Haematopoietic Stem Cell Transplantation for LRBA Deficiency with Fludarabine, Treosulfan, and Thiotepa-Based Conditioning.
Journal: Journal of clinical immunology
Published: January 04, 2024
Two decades of stem cell transplantation in patients with Fanconi anemia: Analysis of factors affecting transplant outcomes.
Journal: Clinical transplantation
Published: July 23, 2022
Incremental donor lymphocyte infusion to treat mixed chimerism after allogeneic stem cell transplantation in children with non-malignant diseases.
Journal: Bone marrow transplantation
Published: July 21, 2022
Autoimmune Cytopenias Post Hematopoietic Stem Cell Transplantation in Pediatric Patients With Osteopetrosis and Other Nonmalignant Diseases.
Journal: Frontiers in immunology
Published: February 20, 2022
Monogenic early-onset lymphoproliferation and autoimmunity: Natural history of STAT3 gain-of-function syndrome.
Journal: The Journal of allergy and clinical immunology
Published: November 03, 2021
A human case of GIMAP6 deficiency: a novel primary immune deficiency.
Journal: European journal of human genetics : EJHG
Published: February 10, 2020
The Broad Clinical Spectrum and Transplant Results of PNP Deficiency.
Journal: Journal of clinical immunology
Published: July 10, 2019
Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations.
Journal: The Journal of allergy and clinical immunology
Published: July 08, 2019
Combined immunodeficiency and atopy caused by a dominant negative mutation in caspase activation and recruitment domain family member 11 (CARD11).
Journal: The Journal of allergy and clinical immunology
Published: February 20, 2017
Showing 1-10 of 10
Last Updated: 09/26/2026