I. Ivanov

I. Ivanov, M. Neshterova, 1998, European journal of ultrasound : official journal of the European Federation of Societies for Ultrasound in Medicine and Biology.

Identification of mtDNA 7028C and 16519T Polymorphisms in a Pediatric-Onset Cyclic Vomiting Syndrome (CVS) Patient

N. Popov, I. Ivanov, B. H. Teneva, 2013 .

D. Dimitrova, T. Todorov, A. Todorova, 2018, Front. Pediatr..

Aniridia: Recent achievements in paediatric practice

M. Snir, M. Shohat, A. Shuper, 1995, European Journal of Pediatrics.

Heterogeneous seizure manifestations in Hypomelanosis of Ito: report of four new cases and review of the literature

P. Striano, P. Bramanti, P. Genton, 2010, Neurological Sciences.

Profiling of Circulating Serum MicroRNAs in Children with Autism Spectrum Disorder using Stem-loop qRT-PCR Assay

N. Popov, I. Ivanov, T. Vachev, 2017, Folia medica.

Epilepsy in Children with Autistic Spectrum Disorder

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

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

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

Phenotype and 244k array‐CGH characterization of chromosome 13q deletions: An update of the phenotypic map of 13q21.1‐qter

J. Fryns, M. Kirchhoff, C. Fagerberg, 2009, American journal of medical genetics. Part A.

Central Nervous System Involvement in Henoch-Schonlein Purpura in Children and Adolescents

P. Stefanova, I. Pacheva, I. Ivanov, 2017, Case reports in pediatrics.

Cerebellar gangliocytoma presenting with hemifacial spasms: clinical report, literature review and possible mechanisms

E. Naydenov, K. Minkin, I. Ivanov, 2008, Acta Neurochirurgica.

Does lenticulostriate vasculopathy predipose to ischemic brain infarct? A case report

I. Pacheva, I. Ivanov, D. Zlatareva, 2012, Journal of clinical ultrasound : JCU.

B. Peterlin, A. Maver, V. Mitev, 2021, Neuromuscular Disorders.

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.

Prevalence of Cytomegalovirus Infection in Hospitalized Infants

R. Stefanov, D. Terzieva, I. Ivanov, 2012, Folia medica.

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.

Hodgkin's Disease with Atypical Clinical Presentation, Associated with Ataxia-Telangiectasia

I. Ivanov, J. Grudeva-Popova, M. Spasova, 2009 .

Developmental performance of 5‐year‐old Bulgarian children—An example of translational neuroscience in practice

I. Ivanov, R. Yordanova, 2018, Journal of evaluation in clinical practice.

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 .

Cardiac MRI with late gadolinium enhancement shows cardiac involvement 3–6 months after severe acute COVID-19 similar to or worse than PIMS

I. Ivanov, Ivanka N. Paskaleva, S. Stoencheva, 2023, Frontiers in Cardiovascular Medicine.