Geeta M. Govindaraj

Kozhikode, KL, India

Last Updated: 09/26/2026

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Found 18 publications

Hepatosplenic abscesses in a child with p40phox deficiency due to a homozygous NCF4 variant.

Hepatosplenic abscesses in a child with p40phox deficiency due to a homozygous NCF4 variant.

Journal: Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology

Published: May 27, 2025

Identification and Functional Validation of Novel Pathogenic Variants in Primary Immunodeficiencies.

Identification and Functional Validation of Novel Pathogenic Variants in Primary Immunodeficiencies.

Journal: European journal of immunology

Published: November 21, 2024

Immunodeficiency-Related Vaccine-Derived Poliovirus (iVDPV) Excretion in an Infant with Severe Combined Immune Deficiency with Spillover to a Parent.

Immunodeficiency-Related Vaccine-Derived Poliovirus (iVDPV) Excretion in an Infant with Severe Combined Immune Deficiency with Spillover to a Parent.

Journal: Vaccines

Published: April 08, 2024

Genetic landscape of congenital insensitivity to pain and hereditary sensory and autonomic neuropathies.

Genetic landscape of congenital insensitivity to pain and hereditary sensory and autonomic neuropathies.

Journal: Brain : a journal of neurology

Published: April 26, 2023

Assessment of Enterovirus Excretion and Identification of VDPVs in Patients with Primary Immunodeficiency in India: Outcome of ICMR-WHO Collaborative Study Phase-I.

Assessment of Enterovirus Excretion and Identification of VDPVs in Patients with Primary Immunodeficiency in India: Outcome of ICMR-WHO Collaborative Study Phase-I.

Journal: Vaccines

Published: March 07, 2023

Infections in Inborn Errors of Immunity with Combined Immune Deficiency: A Review.

Infections in Inborn Errors of Immunity with Combined Immune Deficiency: A Review.

Journal: Pathogens (Basel, Switzerland)

Published: December 08, 2022

Epilepsy of infancy with migrating focal seizures due to a novel homozygous mutation in KCNT1 gene: A case report.

Epilepsy of infancy with migrating focal seizures due to a novel homozygous mutation in KCNT1 gene: A case report.

Journal: Seizure

Published: October 06, 2022

X-Linked Agammaglobulinemia and COVID-19: Two Case Reports and Review of Literature.

X-Linked Agammaglobulinemia and COVID-19: Two Case Reports and Review of Literature.

Journal: Pediatric allergy, immunology, and pulmonology

Published: September 08, 2021

Whole genome sequencing identifies novel structural variant in a large Indian family affected with X-linked agammaglobulinemia.

Whole genome sequencing identifies novel structural variant in a large Indian family affected with X-linked agammaglobulinemia.

Journal: PloS one

Published: December 09, 2020

Clinical Profile of Hyper-IgE Syndrome in India.

Clinical Profile of Hyper-IgE Syndrome in India.

Journal: Frontiers in immunology

Published: November 06, 2020

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

Spectrum of clinical features and genetic variants in mevalonate kinase (MVK) gene of South Indian families suffering from Hyperimmunoglobulin D Syndrome.

Spectrum of clinical features and genetic variants in mevalonate kinase (MVK) gene of South Indian families suffering from Hyperimmunoglobulin D Syndrome.

Journal: PloS one

Published: April 29, 2020

Showing 1-12 of 18

Last Updated: 09/26/2026