George Shubinsky
Rager Avenue
Beersheba, D, Israel
Beersheba, D, Israel
Last Updated: 09/26/2026
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Found 9 publications
X-linked C1GALT1C1 mutation causes atypical hemolytic uremic syndrome.
Journal: European journal of human genetics : EJHG
Published: October 13, 2022
Hypoparathyroidism-Retardation-Dysmorphism Syndrome due to a Variant in the Tubulin-Specific Chaperone E Gene as a Cause of Combined Immune Deficiency.
Journal: Journal of clinical immunology
Published: June 27, 2022
Hyper IgM in tricho-hepato-enteric syndrome due to TTC37 mutation.
Journal: Immunologic research
Published: March 30, 2022
A novel zeta-associated protein 70 homozygous mutation causing combined immunodeficiency presenting as neonatal autoimmune hemolytic anemia.
Journal: Immunologic research
Published: September 25, 2020
Unusual phenotype in patients with a hypomorphic mutation in the DCLRE1C gene: IgG hypergammaglobulinemia with IgA and IgE deficiency.
Journal: Clinical immunology (Orlando, Fla.)
Published: November 20, 2019
Mycophenolate Mofetil Alone and in Combination with Tacrolimus Inhibits the Proliferation of HT-29 Human Colonic Adenocarcinoma Cell Line and Might Interfere with Colonic Tumorigenesis.
Journal: Anticancer research
Published: April 04, 2018
The clinical and laboratory spectrum of dedicator of cytokinesis 8 immunodeficiency syndrome in patients with a unique mutation.
Journal: Immunologic research
Published: January 11, 2017
Reed-Sternberg cells in Hodgkin's lymphoma present features of cellular senescence.
Journal: Cell death & disease
Published: October 01, 2015
Showing 1-9 of 9
Last Updated: 09/26/2026