Gouri P. Hule

Mumbai, MH, India

Last Updated: 09/26/2026

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Found 16 publications

Mendelian susceptibility to mycobacterial disease: Clinical, immunological, and genetic study in India.

Mendelian susceptibility to mycobacterial disease: Clinical, immunological, and genetic study in India.

Journal: Journal of human immunity

Published: July 12, 2025

Common Variable Immunodeficiency Disorder: A Decade of Insights from a Cohort of 150 Patients in India and the Use of Machine Learning Algorithms to Predict Severity.

Common Variable Immunodeficiency Disorder: A Decade of Insights from a Cohort of 150 Patients in India and the Use of Machine Learning Algorithms to Predict Severity.

Journal: Journal of clinical immunology

Published: October 05, 2024

Prenatal Diagnosis for Primary Immunodeficiency Disorders-An Overview of the Indian Scenario.

Prenatal Diagnosis for Primary Immunodeficiency Disorders-An Overview of the Indian Scenario.

Journal: Frontiers in immunology

Published: September 30, 2020

The Spectrum of Clinical, Immunological, and Molecular Findings in Familial Hemophagocytic Lymphohistiocytosis: Experience From India.

The Spectrum of Clinical, Immunological, and Molecular Findings in Familial Hemophagocytic Lymphohistiocytosis: Experience From India.

Journal: Frontiers in immunology

Published: September 30, 2020

Clinical and Genetic Spectrum of a Large Cohort of Patients With Leukocyte Adhesion Deficiency Type 1 and 3: A Multicentric Study From India.

Clinical and Genetic Spectrum of a Large Cohort of Patients With Leukocyte Adhesion Deficiency Type 1 and 3: A Multicentric Study From India.

Journal: Frontiers in immunology

Published: September 30, 2020

Spectrum of Inborn errors of immunity in a cohort of 90 patients presenting with complications to BCG vaccination in India.

Spectrum of Inborn errors of immunity in a cohort of 90 patients presenting with complications to BCG vaccination in India.

Journal: Scandinavian journal of immunology

Published: July 04, 2020

"FUT2" a potential genetic modifier in NCF1 deficiency.

"FUT2" a potential genetic modifier in NCF1 deficiency.

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

Published: June 04, 2019

Does Pioglitazone Lead to Neutrophil Extracellular Traps Formation in Chronic Granulomatous Disease Patients?

Does Pioglitazone Lead to Neutrophil Extracellular Traps Formation in Chronic Granulomatous Disease Patients?

Journal: Frontiers in immunology

Published: May 13, 2019

A case of disseminated subcutaneous phaeohyphomycosis caused by Exserohilum rostratum with CARD9 mutation.

A case of disseminated subcutaneous phaeohyphomycosis caused by Exserohilum rostratum with CARD9 mutation.

Journal: Indian journal of dermatology, venereology and leprology

Published: March 01, 2019

Approach to Molecular Diagnosis of Chronic Granulomatous Disease (CGD): an Experience from a Large Cohort of 90 Indian Patients.

Approach to Molecular Diagnosis of Chronic Granulomatous Disease (CGD): an Experience from a Large Cohort of 90 Indian Patients.

Journal: Journal of clinical immunology

Published: August 18, 2018

p47phox-/- Chronic Granulomatous Disease Patient with Incomplete Kawasaki Disease.

p47phox-/- Chronic Granulomatous Disease Patient with Incomplete Kawasaki Disease.

Journal: Journal of clinical immunology

Published: April 12, 2018

Correction to: Diabetes, Renal, and Cardiovascular Disease in p47phox-/- Chronic Granulomatous Disease.

Correction to: Diabetes, Renal, and Cardiovascular Disease in p47phox-/- Chronic Granulomatous Disease.

Journal: Journal of clinical immunology

Published: November 29, 2017

Showing 1-12 of 16

Last Updated: 09/26/2026