Fani Galabova

First case of Roma ethnic origin with Andermann syndrome: A novel frameshift mutation in exon 20 of SLC12A6 gene

T. Todorov, A. Todorova, I. Pacheva, 2019, American journal of medical genetics. Part A.

Epilepsy in Children with Autistic Spectrum Disorder

I. Pacheva, I. Ivanov, Katerina Gaberova, 2019, Children.

Herpes simplex virus infection in Bulgarian patients with neurological diseases

I. Pacheva, Fani Galabova, M. Pishmisheva, 2022, Journal of Clinical Virology Plus.

Founder p.Arg 446* mutation in the PDHX gene explains over half of cases with congenital lactic acidosis in Roma children.

M. Brown, L. Kalaydjieva, R. Horvath, 2014, Molecular genetics and metabolism.

Neurodevelopmental profile at 5 years of a boy with Dravet syndrome– like phenotype: Does SCN1A gene have something in common?

N. Ivanova, I. Ivanov, Anelia Petkova, 2016 .