Nurit Hadad

Beersheba, D, Israel

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 19 publications

Immunological Manifestations in GALE Deficiency: Extending the Spectrum Beyond Thrombocytopenia and Galactosemia.

Immunological Manifestations in GALE Deficiency: Extending the Spectrum Beyond Thrombocytopenia and Galactosemia.

Journal: Journal of clinical immunology

Published: December 04, 2025

Hypoparathyroidism-Retardation-Dysmorphism Syndrome due to a Variant in the Tubulin-Specific Chaperone E Gene as a Cause of Combined Immune Deficiency.

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

Characterization of the binding of cytosolic phospholipase A2 alpha and NOX2 NADPH oxidase in mouse macrophages.

Characterization of the binding of cytosolic phospholipase A2 alpha and NOX2 NADPH oxidase in mouse macrophages.

Journal: Molecular biology reports

Published: November 01, 2021

Early upregulation of cytosolic phospholipase A2α in motor neurons is induced by misfolded SOD1 in a mouse model of amyotrophic lateral sclerosis.

Early upregulation of cytosolic phospholipase A2α in motor neurons is induced by misfolded SOD1 in a mouse model of amyotrophic lateral sclerosis.

Journal: Journal of neuroinflammation

Published: April 01, 2021

Lumenato protects normal human dermal fibroblasts from neutrophil-induced collagen-3 damage in co-cultures.

Lumenato protects normal human dermal fibroblasts from neutrophil-induced collagen-3 damage in co-cultures.

Journal: PloS one

Published: December 02, 2020

A novel zeta-associated protein 70 homozygous mutation causing combined immunodeficiency presenting as neonatal autoimmune hemolytic anemia.

A novel zeta-associated protein 70 homozygous mutation causing combined immunodeficiency presenting as neonatal autoimmune hemolytic anemia.

Journal: Immunologic research

Published: September 25, 2020

Neutrophil Functions in Immunodeficiency Due to DOCK8 Deficiency.

Neutrophil Functions in Immunodeficiency Due to DOCK8 Deficiency.

Journal: Immunological investigations

Published: January 29, 2019

Combination of EPA with Carotenoids and Polyphenol Synergistically Attenuated the Transformation of Microglia to M1 Phenotype Via Inhibition of NF-κB.

Combination of EPA with Carotenoids and Polyphenol Synergistically Attenuated the Transformation of Microglia to M1 Phenotype Via Inhibition of NF-κB.

Journal: Neuromolecular medicine

Published: February 28, 2017

The clinical and laboratory spectrum of dedicator of cytokinesis 8 immunodeficiency syndrome in patients with a unique mutation.

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

Regulatory role of cytosolic phospholipase A2 alpha in the induction of CD40 in microglia.

Regulatory role of cytosolic phospholipase A2 alpha in the induction of CD40 in microglia.

Journal: Journal of neuroinflammation

Published: October 19, 2016

Reduction of cytosolic phospholipase A2α upregulation delays the onset of symptoms in SOD1G93A mouse model of amyotrophic lateral sclerosis.

Reduction of cytosolic phospholipase A2α upregulation delays the onset of symptoms in SOD1G93A mouse model of amyotrophic lateral sclerosis.

Journal: Journal of neuroinflammation

Published: April 06, 2016

Cytosolic phospholipase A2 α has a crucial role in the pathogenesis of DSS-induced colitis in mice.

Cytosolic phospholipase A2 α has a crucial role in the pathogenesis of DSS-induced colitis in mice.

Journal: European journal of immunology

Published: June 08, 2015

Showing 1-12 of 19

Last Updated: 09/26/2026