Poduri A - Search Results

1

Polymicrogyria-associated epilepsy: a multicenter phenotypic study from the Epilepsy Phenome/Genome Project.

Shain C, Ramgopal S, Fallil Z, Parulkar I, Alongi R, Knowlton R, Poduri A; EPGP Investigators. Shain C, et al. Among authors: poduri a. Epilepsia. 2013 Aug;54(8):1368-75. doi: 10.1111/epi.12238. Epub 2013 Jun 10. Epilepsia. 2013. PMID: 23750890 Free PMC article.

2

A distinct asymmetrical pattern of cortical malformation: large unilateral malformation of cortical development with contralateral periventricular nodular heterotopia in three pediatric cases.

Poduri A, Golja A, Riviello JJ Jr, Bourgeois BF, Duffy FH, Takeoka M. Poduri A, et al. Epilepsia. 2005 Aug;46(8):1317-21. doi: 10.1111/j.1528-1167.2005.07005.x. Epilepsia. 2005. PMID: 16060947 Free article.

3

Focal cortical malformations can show asymmetrically higher uptake on interictal fluorine-18 fluorodeoxyglucose positron emission tomography (PET).

Poduri A, Golja A, Takeoka M, Bourgeois BF, Connolly L, Riviello JJ Jr. Poduri A, et al. J Child Neurol. 2007 Feb;22(2):232-7. doi: 10.1177/0883073807300305. J Child Neurol. 2007. PMID: 17621491

4

Oxcarbazepine in children with nocturnal frontal-lobe epilepsy.

Raju GP, Sarco DP, Poduri A, Riviello JJ, Bergin AM, Takeoka M. Raju GP, et al. Among authors: poduri a. Pediatr Neurol. 2007 Nov;37(5):345-9. doi: 10.1016/j.pediatrneurol.2007.06.013. Pediatr Neurol. 2007. PMID: 17950420 Clinical Trial.

5

The syndrome of perisylvian polymicrogyria with congenital arthrogryposis.

Poduri A, Chitsazzadeh V, D'Arrigo S, Fedrizzi E, Pantaleoni C, Riva D, Busse C, Küster H, Duplessis A, Gaitanis J, Sahin M, Garganta C, Topcu M, Dies KA, Barry BJ, Partlow J, Barkovich AJ, Walsh CA, Chang BS. Poduri A, et al. Brain Dev. 2010 Aug;32(7):550-5. doi: 10.1016/j.braindev.2009.08.005. Epub 2009 Sep 13. Brain Dev. 2010. PMID: 19751967 Free PMC article.

6

Novel susceptibility locus at chromosome 6q16.3-22.31 in a family with GEFS+.

Poduri A, Wang Y, Gordon D, Barral-Rodriguez S, Barker-Cummings C, Ulgen A, Chitsazzadeh V, Hill RS, Risch N, Hauser WA, Pedley TA, Walsh CA, Ottman R. Poduri A, et al. Neurology. 2009 Oct 20;73(16):1264-72. doi: 10.1212/WNL.0b013e3181bd10d3. Neurology. 2009. PMID: 19841378 Free PMC article.

7

Candidate gene sequencing of LHX2, HESX1, and SOX2 in a large schizencephaly cohort.

Mellado C, Poduri A, Gleason D, Elhosary PC, Barry BJ, Partlow JN, Chang BS, Shaw GM, Barkovich AJ, Walsh CA. Mellado C, et al. Among authors: poduri a. Am J Med Genet A. 2010 Nov;152A(11):2736-42. doi: 10.1002/ajmg.a.33684. Am J Med Genet A. 2010. PMID: 20949537 Free PMC article.

8

Rufinamide for the treatment of epileptic spasms.

Olson HE, Loddenkemper T, Vendrame M, Poduri A, Takeoka M, Bergin AM, Libenson MH, Duffy FH, Rotenberg A, Coulter D, Bourgeois BF, Kothare SV. Olson HE, et al. Among authors: poduri a. Epilepsy Behav. 2011 Feb;20(2):344-8. doi: 10.1016/j.yebeh.2010.11.023. Epub 2011 Jan 13. Epilepsy Behav. 2011. PMID: 21233024

9

Epilepsy genetics--past, present, and future.

Poduri A, Lowenstein D. Poduri A, et al. Curr Opin Genet Dev. 2011 Jun;21(3):325-32. doi: 10.1016/j.gde.2011.01.005. Epub 2011 Jan 27. Curr Opin Genet Dev. 2011. PMID: 21277190 Free PMC article. Review.

10

The Epilepsy Phenome/Genome Project (EPGP) informatics platform.

Nesbitt G, McKenna K, Mays V, Carpenter A, Miller K, Williams M; EPGP Investigators. Nesbitt G, et al. Int J Med Inform. 2013 Apr;82(4):248-59. doi: 10.1016/j.ijmedinf.2012.03.004. Epub 2012 May 10. Int J Med Inform. 2013. PMID: 22579394 Free PMC article.

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