Todorova, A., Genetic Medico-Diagnostic Laboratory „Genica” - Sofia; Medical university – Sofia, Bulgaria
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Bulgarian Neurology Vol. 21 No. 2 (2020): Bulgarian Neurology - REVIEWS
Leukodystrophies and leukoencephalopathies in childhood – classification, diagnosis and treatment
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Bulgarian Neurology Vol. 22 No. 1 (2021): Bulgarian Neurology - CASE REPORT
Congenital myotonia caused by a mutation in the SCN4A gene
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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. 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. 24 No. 2 (2023): Bulgarian Neurology - ORIGINAL PAPERS
Treatment effect of Spinraza (Nusinersen) in adult patients with spinal muscular atrophy
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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. 2 (2019): Bulgarian Neurology - ORIGINAL PAPERS
Limb girdle muscular dystrophy 2G in a religious minority of bulgarian muslims homozygous for the c.75g>a, p. trp25x mutation
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