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Neurologic phenotypes associated with COL4A1/2 mutations: Expanding the spectrum of disease.
Zagaglia S, Selch C, Nisevic JR, Mei D, Michalak Z, Hernandez-Hernandez L, Krithika S, Vezyroglou K, Varadkar SM, Pepler A, Biskup S, Leão M, Gärtner J, Merkenschlager A, Jaksch M, Møller RS, Gardella E, Kristiansen BS, Hansen LK, Vari MS, Helbig KL, Desai S, Smith-Hicks CL, Hino-Fukuyo N, Talvik T, Laugesaar R, Ilves P, Õunap K, Körber I, Hartlieb T, Kudernatsch M, Winkler P, Schimmel M, Hasse A, Knuf M, Heinemeyer J, Makowski C, Ghedia S, Subramanian GM, Striano P, Thomas RH, Micallef C, Thom M, Werring DJ, Kluger GJ, Cross JH, Guerrini R, Balestrini S, Sisodiya SM. Zagaglia S, et al. Among authors: sisodiya sm. Neurology. 2018 Nov 27;91(22):e2078-e2088. doi: 10.1212/WNL.0000000000006567. Epub 2018 Nov 9. Neurology. 2018. PMID: 30413629 Free PMC article.
Microdysgenesis in mesial temporal lobe epilepsy.
Eriksson SH, Nordborg C, Thom M, Sisodiya SM. Eriksson SH, et al. Among authors: sisodiya sm. Ann Neurol. 2004 Apr;55(4):596-7; author reply 597. doi: 10.1002/ana.20056. Ann Neurol. 2004. PMID: 15048903 No abstract available.
Increased NKCC1 expression in refractory human epilepsy.
Sen A, Martinian L, Nikolic M, Walker MC, Thom M, Sisodiya SM. Sen A, et al. Among authors: sisodiya sm. Epilepsy Res. 2007 May;74(2-3):220-7. doi: 10.1016/j.eplepsyres.2007.01.004. Epub 2007 Mar 6. Epilepsy Res. 2007. PMID: 17344024
414 results