Ankita Singh

Chandigarh, CH 160012, India

Last Updated: 09/26/2026

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Found 19 publications

Association of SNP (rs1042579) in thrombomodulin gene and plasma thrombomodulin level in North Indian children with Kawasaki disease.

Association of SNP (rs1042579) in thrombomodulin gene and plasma thrombomodulin level in North Indian children with Kawasaki disease.

Journal: Molecular biology reports

Published: March 07, 2022

Features of Hemophagocytic Lymphohistiocytosis in Infants With Severe Combined Immunodeficiency: Our Experience From Chandigarh, North India.

Features of Hemophagocytic Lymphohistiocytosis in Infants With Severe Combined Immunodeficiency: Our Experience From Chandigarh, North India.

Journal: Frontiers in immunology

Published: February 01, 2022

Skewed TCR Alpha, but not Beta, Gene Rearrangements and Lymphoma Associated with a Pathogenic TRAC Variant.

Skewed TCR Alpha, but not Beta, Gene Rearrangements and Lymphoma Associated with a Pathogenic TRAC Variant.

Journal: Journal of clinical immunology

Published: February 18, 2021

Clinical, Immunological, and Molecular Features of Severe Combined Immune Deficiency: A Multi-Institutional Experience From India.

Clinical, Immunological, and Molecular Features of Severe Combined Immune Deficiency: A Multi-Institutional Experience From India.

Journal: Frontiers in immunology

Published: October 19, 2020

Successful perioperative management of three patients with hereditary angioedema without C1 esterase inhibitor therapy: A developing country perspective.

Successful perioperative management of three patients with hereditary angioedema without C1 esterase inhibitor therapy: A developing country perspective.

Journal: Immunobiology

Published: July 21, 2020

Importance of Morphology in the Era of Molecular Biology: Lesson Learnt from a Case of Chediak-Higashi Syndrome.

Importance of Morphology in the Era of Molecular Biology: Lesson Learnt from a Case of Chediak-Higashi Syndrome.

Journal: Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion

Published: May 06, 2020

Clinico-laboratory profile of Kawasaki disease with arthritis in children.

Clinico-laboratory profile of Kawasaki disease with arthritis in children.

Journal: European journal of pediatrics

Published: October 05, 2019

LACC1 gene mutation in three sisters with polyarthritis without systemic features.

LACC1 gene mutation in three sisters with polyarthritis without systemic features.

Journal: Annals of the rheumatic diseases

Published: September 10, 2019

An updated review on phenocopies of primary immunodeficiency diseases.

An updated review on phenocopies of primary immunodeficiency diseases.

Journal: Genes & diseases

Published: July 01, 2019

Severe Lip Involvement in Kawasaki Disease: A Clinical Oddity.

Severe Lip Involvement in Kawasaki Disease: A Clinical Oddity.

Journal: Journal of clinical rheumatology : practical reports on rheumatic & musculoskeletal diseases

Published: May 25, 2019

Genetics of severe combined immunodeficiency.

Genetics of severe combined immunodeficiency.

Journal: Genes & diseases

Published: April 10, 2019

An updated review on activated PI3 kinase delta syndrome (APDS).

An updated review on activated PI3 kinase delta syndrome (APDS).

Journal: Genes & diseases

Published: April 01, 2019

Showing 1-12 of 19

Last Updated: 09/26/2026