Thio LL - Search Results

1

Gain-of-function HCN2 variants in genetic epilepsy.

Li M, Maljevic S, Phillips AM, Petrovski S, Hildebrand MS, Burgess R, Mount T, Zara F, Striano P, Schubert J, Thiele H, Nürnberg P, Wong M, Weisenberg JL, Thio LL, Lerche H, Scheffer IE, Berkovic SF, Petrou S, Reid CA. Li M, et al. Among authors: thio ll. Hum Mutat. 2018 Feb;39(2):202-209. doi: 10.1002/humu.23357. Epub 2017 Nov 13. Hum Mutat. 2018. PMID: 29064616

2

Ketone bodies do not directly alter excitatory or inhibitory hippocampal synaptic transmission.

Thio LL, Wong M, Yamada KA. Thio LL, et al. Neurology. 2000 Jan 25;54(2):325-31. doi: 10.1212/wnl.54.2.325. Neurology. 2000. PMID: 10668691

3

Leptin inhibits 4-aminopyridine- and pentylenetetrazole-induced seizures and AMPAR-mediated synaptic transmission in rodents.

Xu L, Rensing N, Yang XF, Zhang HX, Thio LL, Rothman SM, Weisenfeld AE, Wong M, Yamada KA. Xu L, et al. Among authors: thio ll. J Clin Invest. 2008 Jan;118(1):272-80. doi: 10.1172/JCI33009. J Clin Invest. 2008. PMID: 18097472 Free PMC article.

4

Increased severity of pentylenetetrazol induced seizures in leptin deficient ob/ob mice.

Erbayat-Altay E, Yamada KA, Wong M, Thio LL. Erbayat-Altay E, et al. Among authors: thio ll. Neurosci Lett. 2008 Mar 12;433(2):82-6. doi: 10.1016/j.neulet.2007.12.051. Epub 2007 Dec 28. Neurosci Lett. 2008. PMID: 18241989

5

The ketogenic diet inhibits the mammalian target of rapamycin (mTOR) pathway.

McDaniel SS, Rensing NR, Thio LL, Yamada KA, Wong M. McDaniel SS, et al. Among authors: thio ll. Epilepsia. 2011 Mar;52(3):e7-11. doi: 10.1111/j.1528-1167.2011.02981.x. Epub 2011 Mar 3. Epilepsia. 2011. PMID: 21371020 Free PMC article.

6

Evidence for a shared genetic susceptibility to migraine and epilepsy.

Winawer MR, Connors R; EPGP Investigators. Winawer MR, et al. Epilepsia. 2013 Feb;54(2):288-95. doi: 10.1111/epi.12072. Epub 2013 Jan 7. Epilepsia. 2013. PMID: 23294289 Free PMC article.

7

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. Epilepsia. 2013 Aug;54(8):1368-75. doi: 10.1111/epi.12238. Epub 2013 Jun 10. Epilepsia. 2013. PMID: 23750890 Free PMC article.

8

Lennox-Gastaut syndrome of unknown cause: phenotypic characteristics of patients in the Epilepsy Phenome/Genome Project.

Widdess-Walsh P, Dlugos D, Fahlstrom R, Joshi S, Shellhaas R, Boro A, Sullivan J, Geller E; EPGP Investigators. Widdess-Walsh P, et al. Epilepsia. 2013 Nov;54(11):1898-904. doi: 10.1111/epi.12395. Epub 2013 Oct 7. Epilepsia. 2013. PMID: 24116958 Free article.

9

Racial and ethnic differences in epilepsy classification among probands in the Epilepsy Phenome/Genome Project (EPGP).

Friedman D, Fahlstrom R; EPGP Investigators. Friedman D, et al. Epilepsy Res. 2013 Dec;107(3):306-10. doi: 10.1016/j.eplepsyres.2013.09.007. Epub 2013 Oct 1. Epilepsy Res. 2013. PMID: 24139856 Free PMC article.

10

Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies.

International League Against Epilepsy Consortium on Complex Epilepsies. International League Against Epilepsy Consortium on Complex Epilepsies. Nat Commun. 2018 Dec 10;9(1):5269. doi: 10.1038/s41467-018-07524-z. Nat Commun. 2018. PMID: 30531953 Free PMC article.

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