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Page 1
Gene expression analysis in absence epilepsy using a monozygotic twin design.
Helbig I, Matigian NA, Vadlamudi L, Lawrence KM, Bayly MA, Bain SM, Diyagama D, Scheffer IE, Mulley JC, Holloway AJ, Dibbens LM, Berkovic SF, Hayward NK. Helbig I, et al. Among authors: vadlamudi l. Epilepsia. 2008 Sep;49(9):1546-54. doi: 10.1111/j.1528-1167.2008.01630.x. Epub 2008 Apr 24. Epilepsia. 2008. PMID: 18435749 Free article.
Genetics of temporal lobe epilepsy.
Vadlamudi L, Scheffer IE, Berkovic SF. Vadlamudi L, et al. J Neurol Neurosurg Psychiatry. 2003 Oct;74(10):1359-61. doi: 10.1136/jnnp.74.10.1359. J Neurol Neurosurg Psychiatry. 2003. PMID: 14570824 Free PMC article. No abstract available.
Is benign rolandic epilepsy genetically determined?
Vadlamudi L, Harvey AS, Connellan MM, Milne RL, Hopper JL, Scheffer IE, Berkovic SF. Vadlamudi L, et al. Ann Neurol. 2004 Jul;56(1):129-32. doi: 10.1002/ana.20153. Ann Neurol. 2004. PMID: 15236411
Array-based gene discovery with three unrelated subjects shows SCARB2/LIMP-2 deficiency causes myoclonus epilepsy and glomerulosclerosis.
Berkovic SF, Dibbens LM, Oshlack A, Silver JD, Katerelos M, Vears DF, Lüllmann-Rauch R, Blanz J, Zhang KW, Stankovich J, Kalnins RM, Dowling JP, Andermann E, Andermann F, Faldini E, D'Hooge R, Vadlamudi L, Macdonell RA, Hodgson BL, Bayly MA, Savige J, Mulley JC, Smyth GK, Power DA, Saftig P, Bahlo M. Berkovic SF, et al. Among authors: vadlamudi l. Am J Hum Genet. 2008 Mar;82(3):673-84. doi: 10.1016/j.ajhg.2007.12.019. Epub 2008 Feb 28. Am J Hum Genet. 2008. PMID: 18308289 Free PMC article.
34 results