Schafiq Nabhani

Duesseldorf, NW, Germany

Last Updated: 09/26/2026

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Found 12 publications

Unveiling the Mechanism: Injectable Poly-L-Lactic Acid's Evolving Role-Insights From Recent Studies.

Unveiling the Mechanism: Injectable Poly-L-Lactic Acid's Evolving Role-Insights From Recent Studies.

Journal: Journal of cosmetic dermatology

Published: May 24, 2024

Activity of amorolfine or ciclopirox in combination with terbinafine against pathogenic fungi in onychomycosis-Results of an in vitro investigation.

Activity of amorolfine or ciclopirox in combination with terbinafine against pathogenic fungi in onychomycosis-Results of an in vitro investigation.

Journal: Mycoses

Published: December 20, 2023

Prostaglandin receptor EP4 expression by Th17 cells is associated with high disease activity in ankylosing spondylitis.

Prostaglandin receptor EP4 expression by Th17 cells is associated with high disease activity in ankylosing spondylitis.

Journal: Arthritis research & therapy

Published: December 12, 2018

EBV Negative Lymphoma and Autoimmune Lymphoproliferative Syndrome Like Phenotype Extend the Clinical Spectrum of Primary Immunodeficiency Caused by STK4 Deficiency.

EBV Negative Lymphoma and Autoimmune Lymphoproliferative Syndrome Like Phenotype Extend the Clinical Spectrum of Primary Immunodeficiency Caused by STK4 Deficiency.

Journal: Frontiers in immunology

Published: June 29, 2018

STAT3 gain-of-function mutations associated with autoimmune lymphoproliferative syndrome like disease deregulate lymphocyte apoptosis and can be targeted by BH3 mimetic compounds.

STAT3 gain-of-function mutations associated with autoimmune lymphoproliferative syndrome like disease deregulate lymphocyte apoptosis and can be targeted by BH3 mimetic compounds.

Journal: Clinical immunology (Orlando, Fla.)

Published: September 28, 2016

Specific antibody deficiency and autoinflammatory disease extend the clinical and immunological spectrum of heterozygous NFKB1 loss-of-function mutations in humans.

Specific antibody deficiency and autoinflammatory disease extend the clinical and immunological spectrum of heterozygous NFKB1 loss-of-function mutations in humans.

Journal: Haematologica

Published: July 02, 2016

De novo PIK3R1 gain-of-function with recurrent sinopulmonary infections, long-lasting chronic CMV-lymphadenitis and microcephaly.

De novo PIK3R1 gain-of-function with recurrent sinopulmonary infections, long-lasting chronic CMV-lymphadenitis and microcephaly.

Journal: Clinical immunology (Orlando, Fla.)

Published: August 21, 2015

Early-onset Evans syndrome, immunodeficiency, and premature immunosenescence associated with tripeptidyl-peptidase II deficiency.

Early-onset Evans syndrome, immunodeficiency, and premature immunosenescence associated with tripeptidyl-peptidase II deficiency.

Journal: Blood

Published: November 22, 2014

Autoimmune lymphoproliferative syndrome-like disease in patients with LRBA mutation.

Autoimmune lymphoproliferative syndrome-like disease in patients with LRBA mutation.

Journal: Clinical immunology (Orlando, Fla.)

Published: November 10, 2014

A novel homozygous Fas ligand mutation leads to early protein truncation, abrogation of death receptor and reverse signaling and a severe form of the autoimmune lymphoproliferative syndrome.

A novel homozygous Fas ligand mutation leads to early protein truncation, abrogation of death receptor and reverse signaling and a severe form of the autoimmune lymphoproliferative syndrome.

Journal: Clinical immunology (Orlando, Fla.)

Published: October 07, 2014

Deregulation of Fas ligand expression as a novel cause of autoimmune lymphoproliferative syndrome-like disease.

Deregulation of Fas ligand expression as a novel cause of autoimmune lymphoproliferative syndrome-like disease.

Journal: Haematologica

Published: July 30, 2014

The cell cycle regulator CCDC6 is a key target of RNA-binding protein EWS.

The cell cycle regulator CCDC6 is a key target of RNA-binding protein EWS.

Journal: PloS one

Published: May 08, 2014

Showing 1-12 of 12

Last Updated: 09/26/2026