Sashka Zhelyazkova

发表

Seven Years of Selective Genetic Screening Program and Follow-Up of Asymptomatic Carriers With Hereditary Transthyretin Amyloidosis in Bulgaria

T. Todorov, A. Todorova, I. Tournev, 2022, Frontiers in Neurology.

Mosaicism of a missense SCN1A mutation and Dravet syndrome in a Roma/Gypsy family

Josemir W Sander, I. Scheffer, A. Jablensky, 2010, Epileptic disorders : international epilepsy journal with videotape.

Varicella zoster virus infection in neurological patients in Bulgaria

I. Tournev, I. Ivanov, M. Pishmisheva, 2021, Journal of NeuroVirology.

Traditional practices and perceptions of epilepsy among people in Roma communities in Bulgaria

I. Tournev, J. Sander, Sashka Zhelyazkova, 2020, Epilepsy & Behavior.

A novel GEFS+ locus on 12p13.33 in a large Roma family

Josemir W Sander, B. Morar, D. Azmanov, 2011, Epilepsy Research.

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

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

The fine art of vascular wall maintenance. Carriership of XPC, TP53 and APOE polymorphisms may be a risk factor for cerebral vascular accidents in the Bulgarian population

S. Chakarov, I. Tournev, R. Petkova, 2018, Biotechnology & Biotechnological Equipment.

Focal epilepsy of probable temporal lobe origin in a Gypsy family showing linkage to a novel locus on 7p21.3

Josemir W Sander, B. Morar, D. Azmanov, 2011, Epilepsy Research.

Clinical Spectrum and Genetic Variability in Bulgarian Patients with Niemann-Pick Disease Type C

I. Tournev, V. Guergueltcheva, S. Cherninkova, 2016, European Neurology.

Impact of Vutrisiran on Quality of Life and Physical Function in Patients with Hereditary Transthyretin-Mediated Amyloidosis with Polyneuropathy

Karla P. Zepeda, Hansie M Mathelier, J. Felius, 2023, Neurology and Therapy.

Age and Gender Trends in the Prevalence of Markers for Hepatitis E Virus Exposure in the Heterogeneous Bulgarian Population

R. Bruni, A. Ciccaglione, T. Tenev, 2023, Life.

Mosaicism of a missense SCN1A mutation and Dravet syndrome in a Roma/Gypsy family

Josemir W Sander, I. Scheffer, A. Jablensky, 2010, Epileptic disorders : international epilepsy journal with videotape.

Case Report: Transthyretin Glu54Leu—a rare mutation with predominant cardiac phenotype

T. Todorov, A. Todorova, I. Tournev, 2023, Frontiers in cardiovascular medicine.

Global uncertainty in the diagnosis of neurological complications of SARS-CoV-2 infection by both neurologists and non-neurologists: An international inter-observer variability study

Ana Catarina Fonseca, Wong Wai Kit, H. Tan, 2023, Journal of the Neurological Sciences.