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Dalia Kancheva · SciRah

Researcher profile · Semantic Scholar

Dalia Kancheva

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Dalia Kancheva — researcher profile on SciRah

h-index: 2
Works: 2
Citations: 31

Most-cited papers

Founder p.Arg 446* mutation in the PDHX gene explains over half of cases with congenital lactic acidosis in Roma children.
I. Ivanov, D. Azmanov, Mariya Ivanova, T. Chamova +25 more
2014Molecular Genetics and Metabolism19 citations Open access
Semantic Scholar
Three novel SLC2A1 mutations in Bulgarian patients with different forms of genetic generalized epilepsy reflecting the clinical and genetic diversity of GLUT1-deficiency syndrome.
Nevyana Ivanova, V. Peycheva, K. Kamenarova, Dalia Kancheva +12 more
2018Seizure12 citations Open access
Semantic Scholar

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