Edison ES - Search Results

1

Novel frameshift variant (c.409dupG) in SLC25A38 is a common cause of congenital sideroblastic anaemia in the Indian subcontinent.

Ravindra N, Athiyarath R, S E, S S, Kulkarni U, N A F, Korula A, Shaji RV, George B, Edison ES. Ravindra N, et al. Among authors: edison es. J Clin Pathol. 2021 Mar;74(3):157-162. doi: 10.1136/jclinpath-2020-206647. Epub 2020 Jun 30. J Clin Pathol. 2021. PMID: 32605921

2

Hb Lepore in the Indian population.

Shaji RV, Edison ES, Krishnamoorthy R, Chandy M, Srivastava A. Shaji RV, et al. Among authors: edison es. Hemoglobin. 2003 Feb;27(1):7-14. doi: 10.1081/hem-120018431. Hemoglobin. 2003. PMID: 12603088

3

Rapid detection of beta-globin gene mutations and polymorphisms by temporal temperature gradient gel electrophoresis.

Shaji RV, Edison ES, Poonkuzhali B, Srivastava A, Chandy M. Shaji RV, et al. Among authors: edison es. Clin Chem. 2003 May;49(5):777-81. doi: 10.1373/49.5.777. Clin Chem. 2003. PMID: 12709369

4

Hb Showa-Yakushiji [beta110(G12)Leu-->Pro] in four unrelated patients from west Bengal.

Edison ES, Shaji RV, Devi SG, Kumar SS, Srivastava A, Chandy M. Edison ES, et al. Hemoglobin. 2005;29(1):19-25. Hemoglobin. 2005. PMID: 15768552

5

Hyperbilirubinemia in homozygous HbE disease is associated with the UGT1A1 gene polymorphism.

Edison ES, Shaji RV, Srivastava A, Chandy M. Edison ES, et al. Hemoglobin. 2005;29(3):189-95. doi: 10.1081/hem-200066314. Hemoglobin. 2005. PMID: 16114182

6

Compound heterozygosity for Hb E and Hb Lepore-Hollandia in India; first report and potential diagnostic pitfalls.

Edison ES, Shaji RV, Srivastava A, Chandy M. Edison ES, et al. Hemoglobin. 2005;29(3):221-4. doi: 10.1081/hem-200066327. Hemoglobin. 2005. PMID: 16114186

7

Analysis of beta globin mutations in the Indian population: presence of rare and novel mutations and region-wise heterogeneity.

Edison ES, Shaji RV, Devi SG, Moses A, Viswabandhya A, Mathews V, George B, Srivastava A, Chandy M. Edison ES, et al. Clin Genet. 2008 Apr;73(4):331-7. doi: 10.1111/j.1399-0004.2008.00973.x. Epub 2008 Feb 20. Clin Genet. 2008. PMID: 18294253

8

Interaction of hemoglobin E with other abnormal hemoglobins.

Edison ES, Shaji RV, Chandy M, Srivastava A. Edison ES, et al. Acta Haematol. 2011;126(4):246-8. doi: 10.1159/000329904. Epub 2011 Oct 4. Acta Haematol. 2011. PMID: 21986214 No abstract available.

9

A novel 26 bp deletion [HBB: c.20_45del26bp] in exon 1 of the β-globin gene causing β-thalassemia major.

Edison ES, Venkatesan RS, Govindanattar SD, George B, Shaji RV. Edison ES, et al. Hemoglobin. 2012;36(1):98-102. doi: 10.3109/03630269.2011.641135. Hemoglobin. 2012. PMID: 22233277

10

A novel β-globin gene mutation HBB.c.22 G>C produces a hemoglobin variant (Hb Vellore) mimicking HbS in HPLC.

Edison ES, Sathya M, Rajkumar SV, Nair SC, Srivastava A, Shaji RV. Edison ES, et al. Int J Lab Hematol. 2012 Oct;34(5):556-8. doi: 10.1111/j.1751-553X.2012.01418.x. Epub 2012 Apr 4. Int J Lab Hematol. 2012. PMID: 22471768

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