Enrica Calzoni

Milan, 20132, Italy

Last Updated: 09/26/2026

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Found 13 publications

Multiomics dissection of human RAG deficiency reveals distinctive patterns of immune dysregulation but a common inflammatory signature.

Multiomics dissection of human RAG deficiency reveals distinctive patterns of immune dysregulation but a common inflammatory signature.

Journal: Science immunology
Published: January 10, 2025

Exonic knockout and knockin gene editing in hematopoietic stem and progenitor cells rescues RAG1 immunodeficiency.

Exonic knockout and knockin gene editing in hematopoietic stem and progenitor cells rescues RAG1 immunodeficiency.

Journal: Science translational medicine
Published: February 07, 2024

Transplantation after CD45-ADC corrects Rag1 immunodeficiency in congenic and haploidentical settings.

Transplantation after CD45-ADC corrects Rag1 immunodeficiency in congenic and haploidentical settings.

Journal: The Journal of allergy and clinical immunology
Published: March 31, 2023

Human inborn errors of immunity caused by defects of receptor and proteins of cellular membrane.

Human inborn errors of immunity caused by defects of receptor and proteins of cellular membrane.

Journal: Minerva pediatrica
Published: September 22, 2020

Artificial thymic organoids represent a reliable tool to study T-cell differentiation in patients with severe T-cell lymphopenia.

Artificial thymic organoids represent a reliable tool to study T-cell differentiation in patients with severe T-cell lymphopenia.

Journal: Blood advances
Published: February 24, 2020

Efficacy and safety of anti-CD45-saporin as conditioning agent for RAG deficiency.

Efficacy and safety of anti-CD45-saporin as conditioning agent for RAG deficiency.

Journal: The Journal of allergy and clinical immunology
Published: January 28, 2020

Defining a new immune deficiency syndrome: MAN2B2-CDG.

Defining a new immune deficiency syndrome: MAN2B2-CDG.

Journal: The Journal of allergy and clinical immunology
Published: June 09, 2019

Inborn Errors of Immunity With Immune Dysregulation: From Bench to Bedside.

Inborn Errors of Immunity With Immune Dysregulation: From Bench to Bedside.

Journal: Frontiers in pediatrics
Published: May 08, 2019

Hematopoietic Stem Cell Transplantation in Primary Immunodeficiency Diseases: Current Status and Future Perspectives.

Hematopoietic Stem Cell Transplantation in Primary Immunodeficiency Diseases: Current Status and Future Perspectives.

Journal: Frontiers in pediatrics
Published: May 03, 2019

F-BAR domain only protein 1 (FCHO1) deficiency is a novel cause of combined immune deficiency in human subjects.

F-BAR domain only protein 1 (FCHO1) deficiency is a novel cause of combined immune deficiency in human subjects.

Journal: The Journal of allergy and clinical immunology
Published: January 14, 2019

Corrigendum: Natural Killer Cells from Patients with Recombinase-Activating Gene and Non-Homologous End Joining Gene Defects Comprise a Higher Frequency of CD56bright NKG2A+++ Cells, and Yet Display Increased Degranulation and Higher Perforin Content.

Corrigendum: Natural Killer Cells from Patients with Recombinase-Activating Gene and Non-Homologous End Joining Gene Defects Comprise a Higher Frequency of CD56bright NKG2A+++ Cells, and Yet Display Increased Degranulation and Higher Perforin Content.

Journal: Frontiers in immunology
Published: September 10, 2017

Natural Killer Cells from Patients with Recombinase-Activating Gene and Non-Homologous End Joining Gene Defects Comprise a Higher Frequency of CD56bright NKG2A+++ Cells, and Yet Display Increased Degranulation and Higher Perforin Content.

Natural Killer Cells from Patients with Recombinase-Activating Gene and Non-Homologous End Joining Gene Defects Comprise a Higher Frequency of CD56bright NKG2A+++ Cells, and Yet Display Increased Degranulation and Higher Perforin Content.

Journal: Frontiers in immunology
Published: May 01, 2017
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Last Updated: 09/26/2026