Handunnetthi L - Search Results

1

Prodromal symptoms of multiple sclerosis in primary care.

Disanto G, Zecca C, MacLachlan S, Sacco R, Handunnetthi L, Meier UC, Simpson A, McDonald L, Rossi A, Benkert P, Kuhle J, Ramagopalan SV, Gobbi C. Disanto G, et al. Among authors: handunnetthi l. Ann Neurol. 2018 Jun;83(6):1162-1173. doi: 10.1002/ana.25247. Epub 2018 May 30. Ann Neurol. 2018. PMID: 29740872

2

Multiple sclerosis, vitamin D, and HLA-DRB1*15.

Handunnetthi L, Ramagopalan SV, Ebers GC. Handunnetthi L, et al. Neurology. 2010 Jun 8;74(23):1905-10. doi: 10.1212/WNL.0b013e3181e24124. Neurology. 2010. PMID: 20530326 Free PMC article. Review.

3

The emerging role of vitamin D binding protein in multiple sclerosis.

Disanto G, Ramagopalan SV, Para AE, Handunnetthi L. Disanto G, et al. Among authors: handunnetthi l. J Neurol. 2011 Mar;258(3):353-8. doi: 10.1007/s00415-010-5797-8. Epub 2010 Nov 2. J Neurol. 2011. PMID: 21042807 Review.

4

Genetic and environmental factors and the distribution of multiple sclerosis in Europe.

Handel AE, Handunnetthi L, Giovannoni G, Ebers GC, Ramagopalan SV. Handel AE, et al. Among authors: handunnetthi l. Eur J Neurol. 2010 Sep;17(9):1210-1214. doi: 10.1111/j.1468-1331.2010.03003.x. Epub 2010 Mar 22. Eur J Neurol. 2010. PMID: 20345929

5

An updated meta-analysis of risk of multiple sclerosis following infectious mononucleosis.

Handel AE, Williamson AJ, Disanto G, Handunnetthi L, Giovannoni G, Ramagopalan SV. Handel AE, et al. Among authors: handunnetthi l. PLoS One. 2010 Sep 1;5(9):e12496. doi: 10.1371/journal.pone.0012496. PLoS One. 2010. PMID: 20824132 Free PMC article.

6

Regulatory genomic regions active in immune cell types explain a large proportion of the genetic risk of multiple sclerosis.

Elangovan RI, Disanto G, Berlanga-Taylor AJ, Ramagopalan SV, Handunnetthi L. Elangovan RI, et al. Among authors: handunnetthi l. J Hum Genet. 2014 Apr;59(4):211-5. doi: 10.1038/jhg.2014.3. Epub 2014 Feb 13. J Hum Genet. 2014. PMID: 24522295

7

Risk alleles for multiple sclerosis in multiplex families.

D'Netto MJ, Ward H, Morrison KM, Ramagopalan SV, Dyment DA, DeLuca GC, Handunnetthi L, Sadovnick AD, Ebers GC. D'Netto MJ, et al. Among authors: handunnetthi l. Neurology. 2009 Jun 9;72(23):1984-8. doi: 10.1212/WNL.0b013e3181a92c25. Neurology. 2009. PMID: 19506219

8

Variants in ST8SIA1 do not play a major role in susceptibility to multiple sclerosis in Canadian families.

Ramagopalan SV, Morrison KM, Para A, Handel A, Disanto G, Handunnetthi L, Orton SM, Sadovnick AD, Ebers GC. Ramagopalan SV, et al. Among authors: handunnetthi l. J Neuroimmunol. 2009 Jul 25;212(1-2):142-4. doi: 10.1016/j.jneuroim.2009.04.017. Epub 2009 May 9. J Neuroimmunol. 2009. PMID: 19428123

9

No evidence for an effect of DNA methylation on multiple sclerosis severity at HLA-DRB1*15 or HLA-DRB5.

Handel AE, De Luca GC, Morahan J, Handunnetthi L, Sadovnick AD, Ebers GC, Ramagopalan SV. Handel AE, et al. Among authors: handunnetthi l. J Neuroimmunol. 2010 Jun;223(1-2):120-3. doi: 10.1016/j.jneuroim.2010.03.002. Epub 2010 Apr 14. J Neuroimmunol. 2010. PMID: 20394989

10

Parent-of-origin of HLA-DRB1*1501 and age of onset of multiple sclerosis.

Ramagopalan SV, Byrnes JK, Dyment DA, Guimond C, Handunnetthi L, Disanto G, Yee IM, Ebers GC, Sadovnick AD. Ramagopalan SV, et al. Among authors: handunnetthi l. J Hum Genet. 2009 Sep;54(9):547-9. doi: 10.1038/jhg.2009.69. Epub 2009 Jul 24. J Hum Genet. 2009. PMID: 19629136

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