Jacov Levy
Beersheba, D, Israel
Last Updated: 09/26/2026
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Found 15 publications
One hundred thirty-four germ line PU.1 variants and the agammaglobulinemic patients carrying them.
Journal: Blood
Published: September 09, 2024
Phenotypic variability in patients with unique double homozygous mutations causing variant ataxia telangiectasia.
Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: December 23, 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
Defining the biological responses of IL-6 by the study of a novel IL-6 receptor chain immunodeficiency.
Journal: The Journal of allergy and clinical immunology
Published: May 09, 2019
Neutrophil Functions in Immunodeficiency Due to DOCK8 Deficiency.
Journal: Immunological investigations
Published: January 29, 2019
Incidence of typically Severe Primary Immunodeficiency Diseases in Consanguineous and Non-consanguineous Populations.
Journal: Journal of clinical immunology
Published: January 26, 2017
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
IL-12 receptor 1β deficiency with features of autoimmunity and photosensitivity.
Journal: Autoimmunity
Published: January 14, 2016
Subclinical intestinal inflammation in chronic granulomatous disease patients.
Journal: Immunologic research
Published: November 26, 2015
The effects of Bruton tyrosine kinase inhibition on chemotaxis and superoxide generation in human neutrophils.
Journal: Journal of clinical immunology
Published: August 29, 2013
A novel mutation in SCN9A in a child with congenital insensitivity to pain.
Journal: Pediatric neurology
Published: July 07, 2013
IL-12Rβ1 deficiency: mutation update and description of the IL12RB1 variation database.
Journal: Human mutation
Published: March 15, 2013
Last Updated: 09/26/2026