Koleva, Maya, UHATNP „St. Naum”, Bulgaria
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Bulgarian Neurology Vol. 21 No. 3 (2020): Bulgarian Neurology - CASE REPORT
A case of a 4-year-old girl with multiphase adem and positive anti-mog antibodies
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Bulgarian Neurology Vol. 21 No. 3 (2020): Bulgarian Neurology - CASE REPORT
Familial, genetically verified case of early-onset facioscapulohumeral muscular dystrophy
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Bulgarian Neurology Vol. 21 No. 2 (2020): Bulgarian Neurology - REVIEWS
Neurofibromatosis type I – review of the clinical-genetic, diagnostic and therapeutic aspects and analysis of a bulgarian pediatric population of 40 children. Рart I.
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Bulgarian Neurology Vol. 21 No. 2 (2020): Bulgarian Neurology - ORIGINAL PAPERS
Neurofibromatosis type I – review of the clinical-genetic, diagnostic and therapeutic aspects and analysis of a bulgarian pediatric population of 40 children. Рart II.
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Bulgarian Neurology Vol. 21 No. 1 (2020): Bulgarian Neurology - ORIGINAL PAPERS
Tuberous sclerosis complex - review of the clinical - genetic, diagnostic and therapeutic aspects and analysis of a bulgarian pediatric population of 58 children – part I
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Bulgarian Neurology Vol. 21 No. 1 (2020): Bulgarian Neurology - ORIGINAL PAPERS
Tuberous sclerosis complex - review of the clinical - genetic, diagnostic and therapeutic aspects and analysis of a bulgarian pediatric population of 58 children – part II
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Bulgarian Neurology Vol. 20 No. 1 (2019): Bulgarian Neurology - ORIGINAL PAPERS
Pelizeaus Merzbacher disease - clinically and genetically verified bulgarian case
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Bulgarian Neurology Vol. 20 No. 1 (2019): Bulgarian Neurology - CASE REPORT
Genetically-verified case of neuronal ceroidlipofuscinosis with a novel mutation in CLN6 gene
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Bulgarian Neurology Vol. 20 No. 1 (2019): Bulgarian Neurology - CASE REPORT
Anti-NMDAR encephalitis - rare complication after herpes virus encephalitis with a case report
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