Sirisena ND - Search Results

1

Germline variants of uncertain significance, their frequency, and clinico-pathological features in a cohort of Sri Lankan patients with hereditary breast cancer.

Gunawardena K, Sirisena ND, Anandagoda G, Neththikumara N, Dissanayake VHW. Gunawardena K, et al. Among authors: sirisena nd. BMC Res Notes. 2023 Jun 5;16(1):95. doi: 10.1186/s13104-023-06365-4. BMC Res Notes. 2023. PMID: 37277882 Free PMC article.

2

Carriage rate of hepatitis-B surface antigen (HBsAg) in an urban community in Jos, Plateau State, Nigeria.

Sirisena ND, Njoku MO, Idoko JA, Isamade E, Barau C, Jelpe D, Zamani A, Otowo S. Sirisena ND, et al. Niger Postgrad Med J. 2002 Mar;9(1):7-10. Niger Postgrad Med J. 2002. PMID: 11932753

3

CD4+ T-lymphocyte counts in patients with human immunodeficiency virus type 1 (HIV-1) and healthy population in Jos, Nigeria.

Njoku MO, Sirisena ND, Idoko JA, Jelpe D. Njoku MO, et al. Among authors: sirisena nd. Niger Postgrad Med J. 2003 Sep;10(3):135-9. Niger Postgrad Med J. 2003. PMID: 14692053

4

Candidate gene study of genetic thrombophilic polymorphisms in pre-eclampsia and recurrent pregnancy loss in Sinhalese women.

Dissanayake VH, Sirisena ND, Weerasekera LY, Gammulla CG, Seneviratne HR, Jayasekara RW. Dissanayake VH, et al. Among authors: sirisena nd. J Obstet Gynaecol Res. 2012 Sep;38(9):1168-76. doi: 10.1111/j.1447-0756.2012.01846.x. Epub 2012 Apr 30. J Obstet Gynaecol Res. 2012. PMID: 22540831

5

Prevalence of chromosomal abnormalities in Sri Lankan women with primary amenorrhea.

Samarakoon L, Sirisena ND, Wettasinghe KT, Kariyawasam KW, Jayasekara RW, Dissanayake VH. Samarakoon L, et al. Among authors: sirisena nd. J Obstet Gynaecol Res. 2013 May;39(5):991-7. doi: 10.1111/j.1447-0756.2012.02063.x. Epub 2012 Dec 21. J Obstet Gynaecol Res. 2013. PMID: 23279116

6

A case series of five sri lankan patients with ovotesticular disorder of sex development.

Wettasinghe KT, Sirisena ND, Andraweera PH, Jayasekara RW, Dissanayake VH. Wettasinghe KT, et al. Among authors: sirisena nd. Clin Pediatr Endocrinol. 2012 Oct;21(4):69-73. doi: 10.1297/cpe.21.69. Epub 2012 Oct 30. Clin Pediatr Endocrinol. 2012. PMID: 23926413 Free PMC article.

7

Child with deletion 9p syndrome presenting with craniofacial dysmorphism, developmental delay, and multiple congenital malformations.

Sirisena ND, Wijetunge UK, de Silva R, Dissanayake VH. Sirisena ND, et al. Case Rep Genet. 2013;2013:785830. doi: 10.1155/2013/785830. Epub 2013 Jul 25. Case Rep Genet. 2013. PMID: 23984121 Free PMC article.

8

A child with a novel de novo mutation in the aristaless domain of the aristaless-related homeobox (ARX) gene presenting with ambiguous genitalia and psychomotor delay.

Sirisena ND, McElreavey K, Bashamboo A, de Silva KS, Jayasekara RW, Dissanayake VH. Sirisena ND, et al. Sex Dev. 2014;8(4):156-9. doi: 10.1159/000365458. Epub 2014 Jul 25. Sex Dev. 2014. PMID: 25074490

9

Cytogenetic analysis of chromosomal abnormalities in Sri Lankan children.

Thillainathan S, Sirisena ND, Kariyawasam KW, Jayasekara RW, Dissanayake VH. Thillainathan S, et al. Among authors: sirisena nd. World J Pediatr. 2015 Nov;11(4):374-9. doi: 10.1007/s12519-014-0526-5. Epub 2014 Nov 20. World J Pediatr. 2015. PMID: 25410672

10

Novel COL4A3 gene mutations in a consanguineous family with autosomal recessive Alport syndrome.

Sirisena ND, Thalgahagoda S, Abeyagunawardena A, Neumann M, Schmudlach HO, Jayasekara RW, Dissanayake VH. Sirisena ND, et al. Nephrology (Carlton). 2015 Aug;20(8):580. doi: 10.1111/nep.12430. Nephrology (Carlton). 2015. PMID: 26194984 No abstract available.

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