Laura M. Perez

Combate De Los Pozos 1881, CP
B C1245AAM, Argentina

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 12 publications

Evaluation of Predictive Pharmacokinetic Models to Optimize Infliximab Therapy in Pediatric Inflammatory Bowel Disease.

Evaluation of Predictive Pharmacokinetic Models to Optimize Infliximab Therapy in Pediatric Inflammatory Bowel Disease.

Journal: European journal of drug metabolism and pharmacokinetics

Published: October 02, 2025

Ruptured aortic aneurysm in an adolescent with systemic lupus erythematosus.

Ruptured aortic aneurysm in an adolescent with systemic lupus erythematosus.

Journal: Archivos argentinos de pediatria

Published: October 14, 2024

Monitoring Serum Levels of Infliximab and Anti-Infliximab Antibodies in Pediatric Patients with Inflammatory Bowel Disease: Experience in a High Complexity Pediatric Hospital in Buenos Aires, Argentina

Monitoring Serum Levels of Infliximab and Anti-Infliximab Antibodies in Pediatric Patients with Inflammatory Bowel Disease: Experience in a High Complexity Pediatric Hospital in Buenos Aires, Argentina

Journal: Acta gastroenterologica Latinoamericana

Published: March 26, 2024

Neutralizing IFN-γ autoantibodies are rare and pathogenic in HLA-DRB1*15:02 or 16:02 individuals.

Neutralizing IFN-γ autoantibodies are rare and pathogenic in HLA-DRB1*15:02 or 16:02 individuals.

Journal: The Journal of clinical investigation

Published: December 07, 2023

Human IRF1 governs macrophagic IFN-γ immunity to mycobacteria.

Human IRF1 governs macrophagic IFN-γ immunity to mycobacteria.

Journal: Cell

Published: April 01, 2022

Pulmonary Alveolar Proteinosis and Multiple Infectious Diseases in a Child with Autosomal Recessive Complete IRF8 Deficiency.

Pulmonary Alveolar Proteinosis and Multiple Infectious Diseases in a Child with Autosomal Recessive Complete IRF8 Deficiency.

Journal: Journal of clinical immunology

Published: November 28, 2021

Inherited CARD9 Deficiency in a Patient with Both Exophiala spinifera and Aspergillus nomius Severe Infections.

Inherited CARD9 Deficiency in a Patient with Both Exophiala spinifera and Aspergillus nomius Severe Infections.

Journal: Journal of clinical immunology

Published: November 12, 2019

Inherited p40phox deficiency differs from classic chronic granulomatous disease.

Inherited p40phox deficiency differs from classic chronic granulomatous disease.

Journal: The Journal of clinical investigation

Published: August 30, 2017

Alanine-scanning mutagenesis of human signal transducer and activator of transcription 1 to estimate loss- or gain-of-function variants.

Alanine-scanning mutagenesis of human signal transducer and activator of transcription 1 to estimate loss- or gain-of-function variants.

Journal: The Journal of allergy and clinical immunology

Published: March 28, 2016

Leukocyte Adhesion Deficiency Type 1 (LAD1) with Expressed but Nonfunctional CD11/CD18.

Leukocyte Adhesion Deficiency Type 1 (LAD1) with Expressed but Nonfunctional CD11/CD18.

Journal: Journal of clinical immunology

Published: February 23, 2016

FAS Haploinsufficiency Caused by Extracellular Missense Mutations Underlying Autoimmune Lymphoproliferative Syndrome.

FAS Haploinsufficiency Caused by Extracellular Missense Mutations Underlying Autoimmune Lymphoproliferative Syndrome.

Journal: Journal of clinical immunology

Published: July 12, 2015

Mycobacterial disease in patients with chronic granulomatous disease: A retrospective analysis of 71 cases.

Mycobacterial disease in patients with chronic granulomatous disease: A retrospective analysis of 71 cases.

Journal: The Journal of allergy and clinical immunology

Published: March 15, 2015

Showing 1-12 of 12

Last Updated: 09/26/2026