I. Pacheva

Acute confusional migraine: is it a distinct form of migraine?

I. Pacheva, I. Ivanov, I. Pacheva, 2013, International journal of clinical practice.

Pontocerebellar hypoplasia type 1 for the neuropediatrician: Genotype-phenotype correlations and diagnostic guidelines based on new cases and overview of the literature.

A. Jordanova, I. Litvinenko, A. Savov, 2018, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

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.