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1993 1
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51 results

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Page 1
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: varadkar 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.
Rasmussen's encephalitis: structural, functional, and clinical correlates of contralesional epileptiform activity.
Bauer T, von Wrede RD, Pujar S, Rácz A, Hoppe C, Baumgartner T, Varadkar S, Held NR, Reiter JT, Enders S, David B, Prillwitz CC, Brugues M, Keil VCW, Jeub M, Borger V, Sander JW, Kunz WS, Radbruch A, Weber B, Helmstaedter C, Vatter H, Baldeweg T, Becker AJ, Cross JH, Surges R, Rüber T. Bauer T, et al. Among authors: varadkar s. J Neurol. 2024 Oct;271(10):6680-6691. doi: 10.1007/s00415-024-12607-7. Epub 2024 Aug 14. J Neurol. 2024. PMID: 39138652 Free PMC article.
Inborn errors of metabolism causing epilepsy.
Rahman S, Footitt EJ, Varadkar S, Clayton PT. Rahman S, et al. Among authors: varadkar s. Dev Med Child Neurol. 2013 Jan;55(1):23-36. doi: 10.1111/j.1469-8749.2012.04406.x. Epub 2012 Sep 24. Dev Med Child Neurol. 2013. PMID: 22998469 Free article. Review.
Evolution of the EEG in children with Rasmussen's syndrome.
Longaretti F, Dunkley C, Varadkar S, Vargha-Khadem F, Boyd SG, Cross JH. Longaretti F, et al. Among authors: varadkar s. Epilepsia. 2012 Sep;53(9):1539-45. doi: 10.1111/j.1528-1167.2012.03565.x. Epub 2012 Jun 27. Epilepsia. 2012. PMID: 22738156
51 results