Bojinova, V., UHATNP "St.Naum", Bulgaria
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Bulgarian Neurology Vol. 22 No. 1 (2021): Bulgarian Neurology - CASE REPORT
Polymicrogyria in cases of pathogenic variants in COL18A1 gene, associated with Knobloch syndrome type 1
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Bulgarian Neurology Vol. 22 No. 2 (2021): Bulgarian Neurology - CASE REPORT
Myelinolysis and rhabdomyolysis in a child with severe hypernatremia
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Bulgarian Neurology Vol. 24 No. 3 (2023): Bulgarian Neurology - REVIEWS
Autosomal-dominant and autosomal-recessive form of Juvenile parkinsonism – part I
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Bulgarian Neurology Vol. 24 No. 3 (2023): Bulgarian Neurology - REVIEWS
Juvenile parkinsonism – Dystoniaparkinsonism, Ataxia-parkinsonism, Spastic paraplegia-parkinsonism and Parkinsonism due to brain iron accumulation – part II
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Bulgarian Neurology Vol. 24 No. 3 (2023): Bulgarian Neurology - CASE REPORT
Clinical and MRI characteristics of tubulinopathies. A clinical case of TUBA1A associated pahygiria and cerebellar hypoplasia
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Bulgarian Neurology Vol. 22 No. 1 (2021): Bulgarian Neurology - REVIEWS
Early onset cerebellar ataxia – autosomal recessive forms (Part I)
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Bulgarian Neurology Vol. 22 No. 1 (2021): Bulgarian Neurology - REVIEWS
Early onset cerebellar ataxia – recessive and autosomaldominant forms (Part II)
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Bulgarian Neurology Vol. 25 No. 1 (2024): Bulgarian Neurology - CASE REPORT
Atypical imaging in children with multiple sclerosis – case presentation
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Bulgarian Neurology Vol. 22 No. 1 (2021): Bulgarian Neurology - CASE REPORT
A case of an early onset cerebellar ataxia due to COQ8A mutation
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