N. Ivanova

Hereditary spastic paraplegia 3A associated with axonal neuropathy.

K. Claeys, B. Ceulemans, M. Sereda, 2007, Archives of neurology.

Spastin gene mutations in Bulgarian patients with hereditary spastic paraplegia

V. Timmerman, T. Deconinck, P. de Jonghe, 2006, Clinical genetics.

Chromosomal microarray analysis of Bulgarian patients with epilepsy and intellectual disability.

R. Kaneva, A. Jordanova, I. Litvinenko, 2018, Gene.

Dominant intermediate Charcot-Marie-Tooth type C maps to chromosome 1p34-p35.

V. Timmerman, P. de Jonghe, A. Jordanova, 2003, American journal of human genetics.

CD3Z polymorphisms and promoter hypermethylation in dermatomyositis - the role of cytosine-phosphate-guanine-related single nucleotide polymorphisms

R. Kaneva, D. Kachakova, N. Ivanova, 2021, Immunological investigations.

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 .

Impact of KCNQ2 mutations in Bulgarian patients with electroclinical syndromes with onset in the first year of life

R. Kaneva, A. Jordanova, D. Hristova, 2017 .