Dissanayake VHW - Search Results

1

The first Sri Lankan family with Dent disease-1 due to a pathogenic variant in the CLCN5 gene: a case report.

Ranawaka R, Sirisena ND, Dayasiri KC, Cogal AG, Lieske JC, Gamage MP, Dissanayake VHW. Ranawaka R, et al. Among authors: dissanayake vhw. BMC Res Notes. 2017 Oct 30;10(1):539. doi: 10.1186/s13104-017-2881-5. BMC Res Notes. 2017. PMID: 29084614 Free PMC article.

2

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. 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

3

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. 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

4

A Sri Lankan child with 48,XXXX syndrome.

Padeniya PM, Godapitiya I, Pathirana DR, Jayasekara RW, Dissanayake VH. Padeniya PM, et al. Indian J Pediatr. 2014 Feb;81(2):201-2. doi: 10.1007/s12098-013-0995-x. Epub 2013 Mar 14. Indian J Pediatr. 2014. PMID: 23494840 No abstract available.

5

Autosomal dominant hereditary ataxia in Sri Lanka.

Sumathipala DS, Abeysekera GS, Jayasekara RW, Tallaksen CM, Dissanayake VH. Sumathipala DS, et al. BMC Neurol. 2013 May 1;13:39. doi: 10.1186/1471-2377-13-39. BMC Neurol. 2013. PMID: 23634774 Free PMC article.

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. 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

Clinical and genetic features of Huntington disease in Sri Lanka.

Sumathipala DS, Jayasekara RW, Dissanayake VH. Sumathipala DS, et al. BMC Neurol. 2013 Dec 5;13:191. doi: 10.1186/1471-2377-13-191. BMC Neurol. 2013. PMID: 24314096 Free PMC article.

9

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

10

Cytogenetic analysis of chromosomal abnormalities in Sri Lankan children.

Thillainathan S, Sirisena ND, Kariyawasam KW, Jayasekara RW, Dissanayake VH. Thillainathan S, et al. 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

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