Sickle cell disease in Indian tribal population: Findings of a multi-centre Indian SCD registry-Reference-Cited by-同舟云学术

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Sickle cell disease in Indian tribal population: Findings of a multi-centre Indian SCD registry

Published:2024-11 Issue: Volume:109 Page:102873
ISSN:1079-9796
Container-title:Blood Cells, Molecules, and Diseases
language:en
Short-container-title:Blood Cells, Molecules, and Diseases

Author:

Sharma Yogita^ORCID,Bhat Deepa^ORCID,Sridevi Parikipandla^ORCID,Surti Shaily B.^ORCID,Ranjit Manoranjan^ORCID,Sarmah Jatin^ORCID,Sudhakar Godi^ORCID,Babu Bontha V.^ORCID

Funder

Indian Council of Medical Research

Publisher

Elsevier BV

Reference50 articles.

1. Global burden of sickle cell anaemia in children under five, 2010–2050: modelling based on demographics, excess mortality, and interventions;Piel;PLoS Med.,2013

2. Current Management of Sickle Cell Anemia;Mcgann;Cold Spring Harb. Perspect. Med.,2013

3. Mortality in sickle cell anemia in Africa: a prospective cohort study in Tanzania;Makani;PLoS One,2011

4. Guidelines for National Programme for Prevention & Management of Sickle Cell Disease;Ministry of Health and Family Welfare,2023

5. Variation of HbS frequency in Indian population: role of P.Falciparum and other factors. Indian;Rao;J. Hum. Genet.,1998

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