Gian M. Moneta

Rome, Italy

Last Updated: 09/26/2026

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Found 12 publications

Different patterns of longitudinal changes in antinuclear antibodies titers in children with systemic lupus erythematosus and Sjögren's syndrome.

Different patterns of longitudinal changes in antinuclear antibodies titers in children with systemic lupus erythematosus and Sjögren's syndrome.

Journal: Lupus

Published: November 04, 2024

Persistently active interferon-γ pathway and expansion of T-bet+ B cells in a subset of patients with childhood-onset systemic lupus erythematosus.

Persistently active interferon-γ pathway and expansion of T-bet+ B cells in a subset of patients with childhood-onset systemic lupus erythematosus.

Journal: European journal of immunology

Published: December 06, 2022

Monocytes From Patients With Macrophage Activation Syndrome and Secondary Hemophagocytic Lymphohistiocytosis Are Hyperresponsive to Interferon Gamma.

Monocytes From Patients With Macrophage Activation Syndrome and Secondary Hemophagocytic Lymphohistiocytosis Are Hyperresponsive to Interferon Gamma.

Journal: Frontiers in immunology

Published: February 02, 2021

Movement disorders in ADAR1 disease: Insights from a comprehensive cohort.

Movement disorders in ADAR1 disease: Insights from a comprehensive cohort.

Journal: Parkinsonism & related disorders

Published: May 28, 2020

IFNAR2 Deficiency Causing Dysregulation of NK Cell Functions and Presenting With Hemophagocytic Lymphohistiocytosis.

IFNAR2 Deficiency Causing Dysregulation of NK Cell Functions and Presenting With Hemophagocytic Lymphohistiocytosis.

Journal: Frontiers in genetics

Published: April 24, 2020

The activating p.Ser466Arg change in STAT1 causes a peculiar phenotype with features of interferonopathies.

The activating p.Ser466Arg change in STAT1 causes a peculiar phenotype with features of interferonopathies.

Journal: Clinical genetics

Published: July 22, 2019

An unusual presentation of purine nucleoside phosphorylase deficiency mimicking systemic juvenile idiopathic arthritis complicated by macrophage activation syndrome.

An unusual presentation of purine nucleoside phosphorylase deficiency mimicking systemic juvenile idiopathic arthritis complicated by macrophage activation syndrome.

Journal: Pediatric rheumatology online journal

Published: January 18, 2019

Proprioception sense in lymphedema affected upper limb.

Proprioception sense in lymphedema affected upper limb.

Journal: Lymphology

Published: September 26, 2018

Variable Clinical Phenotypes and Relation of Interferon Signature with Disease Activity in ADA2 Deficiency.

Variable Clinical Phenotypes and Relation of Interferon Signature with Disease Activity in ADA2 Deficiency.

Journal: The Journal of rheumatology

Published: September 13, 2018

Muscle Expression of Type I and Type II Interferons Is Increased in Juvenile Dermatomyositis and Related to Clinical and Histologic Features.

Muscle Expression of Type I and Type II Interferons Is Increased in Juvenile Dermatomyositis and Related to Clinical and Histologic Features.

Journal: Arthritis & rheumatology (Hoboken, N.J.)

Published: December 13, 2017

Switched Memory B Cells Are Increased in Oligoarticular and Polyarticular Juvenile Idiopathic Arthritis and Their Change Over Time Is Related to Response to Tumor Necrosis Factor Inhibitors.

Switched Memory B Cells Are Increased in Oligoarticular and Polyarticular Juvenile Idiopathic Arthritis and Their Change Over Time Is Related to Response to Tumor Necrosis Factor Inhibitors.

Journal: Arthritis & rheumatology (Hoboken, N.J.)

Published: June 24, 2017

Functional and Morphological Improvement of Dystrophic Muscle by Interleukin 6 Receptor Blockade.

Functional and Morphological Improvement of Dystrophic Muscle by Interleukin 6 Receptor Blockade.

Journal: EBioMedicine

Published: November 24, 2014

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Last Updated: 09/26/2026