Athulya Edavazhippurath

Kozhikode, KL, India

Last Updated: 09/26/2026

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Found 9 publications

Skewed X-Chromosome Inactivation in a Child with Fungal Pneumonia and a Pathogenic de novo CYBB Variant.

Skewed X-Chromosome Inactivation in a Child with Fungal Pneumonia and a Pathogenic de novo CYBB Variant.

Journal: Indian journal of pediatrics

Published: December 05, 2025

Subtle Clinical Clues for Early Diagnosis of Lethal ORAI1 Deficiency in Infants.

Subtle Clinical Clues for Early Diagnosis of Lethal ORAI1 Deficiency in Infants.

Journal: Indian journal of pediatrics

Published: November 04, 2025

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

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

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

Clinical, immunological and genomic characteristics of children with X-linked agammaglobulinemia from Kerala, South India.

Clinical, immunological and genomic characteristics of children with X-linked agammaglobulinemia from Kerala, South India.

Journal: Human immunology

Published: June 11, 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

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

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Last Updated: 09/26/2026