Impact of KCNQ2 mutations in Bulgarian patients with electroclinical syndromes with onset in the first year of life by Peycheva, Valentina, Ivanova, Neviana, Kamenarova, Kunka, Tsekova, Irina, Aleksandrova, Iliyana, Bozhinova, Veneta, Bozhidarova, Maria, Litvinenko, Ivan, Hristova, Dimitrina, Mitev, Vanyo, Kaneva, Radka, Jordanova, Albena

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Chromosomal microarray analysis of Bulgarian patients with epilepsy and intellectual disability by Peycheva, Valentina, Kamenarova, Kunka, Ivanova, Neviana, Stamatov, Dimitar, Avdjieva-Tzavella, Daniela, Alexandrova, Iliana, Zhelyazkova, Sashka, Pacheva, Iliana, Dimova, Petya, Ivanov, Ivan, Litvinenko, Ivan, Bozhinova, Veneta, Tournev, Ivailo, Simeonov, Emil, Mitev, Vanyo, Jordanova, Albena, Kaneva, Radka

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Three novel SLC2A1 mutations in Bulgarian patients with different forms of genetic generalized epilepsy reflecting the clinical and genetic diversity of GLUT1-deficiency syndrome by Ivanova, Nevyana, Peycheva, Valentina, Kamenarova, Kunka, Kancheva, Dalia, Tsekova, Irina, Aleksandrova, Iliana, Hristova, Dimitrina, Litvinenko, Ivan, Todorova, Diana, Sarailieva, Gergana, Dimova, Petya, Tomov, Veselin, Bozhinova, Veneta, Mitev, Vanio, Kaneva, Radka, Jordanova, Albena

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Founder p.Arg 446 mutation in the PDHX gene explains over half of cases with congenital lactic acidosis in Roma children by Ivanov, Ivan S., Azmanov, Dimitar N., Ivanova, Mariya B., Chamova, Teodora, Pacheva, Ilyana H., Panova, Margarita V., Song, Sharon, Morar, Bharti, Yordanova, Ralitsa V., Galabova, Fani K., Sotkova, Iglika G., Linev, Alexandar J., Bitchev, Stoyan, Shearwood, Anne-Marie J., Kancheva, Dalia, Gabrikova, Dana, Karcagi, Veronika, Guergueltcheva, Velina, Geneva, Ina E., Bozhinova, Veneta, Stoyanova, Vili K., Kremensky, Ivo, Jordanova, Albena, Savov, Aleksey, Horvath, Rita, Brown, Matthew A., Tournev, Ivailo, Filipovska, Aleksandra, Kalaydjieva, Luba

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