Peter J. Mustillo

Allergy and Immunology

700 Childrens Dr
Columbus, OH 43205

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 16 publications

A de novo dominant-negative PSMB8 mutation causes severe CANDLE/PRAAS due to arrested proteasome biogenesis.

A de novo dominant-negative PSMB8 mutation causes severe CANDLE/PRAAS due to arrested proteasome biogenesis.

Journal: Annals of the rheumatic diseases

Published: July 24, 2025

Germline mutations in a G protein identify signaling cross-talk in T cells.

Germline mutations in a G protein identify signaling cross-talk in T cells.

Journal: Science (New York, N.Y.)

Published: September 19, 2024

Correction to: Clinical Practice Guidelines for the Immunological Management of Chromosome 22q11.2 Deletion Syndrome and Other Defects in Thymic Development.

Correction to: Clinical Practice Guidelines for the Immunological Management of Chromosome 22q11.2 Deletion Syndrome and Other Defects in Thymic Development.

Journal: Journal of clinical immunology

Published: January 22, 2024

The sensitivity of food allergy skin testing soon after food-induced anaphylaxis.

The sensitivity of food allergy skin testing soon after food-induced anaphylaxis.

Journal: The journal of allergy and clinical immunology. In practice

Published: August 07, 2023

COVID-19 Vaccination in Patients with Inborn Errors of Immunity Reduces Hospitalization and Critical Care Needs Related to COVID-19: a USIDNET Report.

COVID-19 Vaccination in Patients with Inborn Errors of Immunity Reduces Hospitalization and Critical Care Needs Related to COVID-19: a USIDNET Report.

Journal: Journal of clinical immunology

Published: August 02, 2023

PI3Kγ in B cells promotes antibody responses and generation of antibody-secreting cells.

PI3Kγ in B cells promotes antibody responses and generation of antibody-secreting cells.

Journal: Nature immunology

Published: July 06, 2023

Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency.

Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency.

Journal: Nature

Published: December 05, 2022

Clinical Practice Guidelines for the Immunological Management of Chromosome 22q11.2 Deletion Syndrome and Other Defects in Thymic Development.

Clinical Practice Guidelines for the Immunological Management of Chromosome 22q11.2 Deletion Syndrome and Other Defects in Thymic Development.

Journal: Journal of clinical immunology

Published: October 10, 2022

Infectious Complications Predict Premature CD8+ T-cell Senescence in CD40 Ligand-Deficient Patients.

Infectious Complications Predict Premature CD8+ T-cell Senescence in CD40 Ligand-Deficient Patients.

Journal: Journal of clinical immunology

Published: November 25, 2020

Delayed-Onset ADA1 (ADA) Deficiency Not Detected by TREC Screen.

Delayed-Onset ADA1 (ADA) Deficiency Not Detected by TREC Screen.

Journal: Pediatrics

Published: November 09, 2020

Coronavirus disease 2019 in patients with inborn errors of immunity: An international study.

Coronavirus disease 2019 in patients with inborn errors of immunity: An international study.

Journal: The Journal of allergy and clinical immunology

Published: July 27, 2020

Severe SARS-CoV-2 disease in the context of a NF-κB2 loss-of-function pathogenic variant.

Severe SARS-CoV-2 disease in the context of a NF-κB2 loss-of-function pathogenic variant.

Journal: The Journal of allergy and clinical immunology

Published: June 26, 2020

Showing 1-12 of 16

Last Updated: 09/26/2026