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Search Results - Abramycheva, Nataliya Yu
Search Results - Abramycheva, Nataliya Yu
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Case report: A novel CACNA1S mutation associated with hypokalemic periodic paralysis
by
Nuzhnyi, Evgenii P.
,
Arestova, Alina S.
,
Rossokhin, Alexey V.
,
Protopopova, Anna O.
,
Abramycheva, Nataliya Yu
,
Suponeva, Natalia A.
,
Illarioshkin, Sergey N.
Published in
Frontiers in neurology
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Second mutation in PARK2 is absent in patients with sporadic Parkinson's disease and heterozygous exonic deletions/duplications in parkin gene
by
Shulskaya, Marina V.
,
Shadrina, Maria I.
,
Fedotova, Ekaterina Yu
,
Abramycheva, Nataliya Yu
,
Limborska, Svetlana A.
,
Illarioshkin, Sergey N.
,
Slominsky, Petr A.
Published in
International journal of neuroscience
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Genetic studies of Russian patients with amyotrophic lateral sclerosis
by
Lysogorskaia, Elena V.
,
Abramycheva, Nataliya Yu
,
Zakharova, Mariya N.
,
Stepanova, Mariya S.
,
Moroz, Anna A.
,
Rossokhin, Alexey V.
,
Illarioshkin, Sergey N.
Published in
Amyotrophic lateral sclerosis and frontotemporal degeneration
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Case report: A novel CACNA1S mutation associated with hypokalemic periodic paralysis
by
Nuzhnyi, Evgenii P
,
Arestova, Alina S
,
Rossokhin, Alexey V
,
Protopopova, Anna O
,
Abramycheva, Nataliya Yu
,
Suponeva, Natalia A
,
Illarioshkin, Sergey N
Published in
Frontiers in neurology
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Amyotrophic Lateral Sclerosis And Frontotemporal Degeneration
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Frontiers In Neurology
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Life Sciences & Biomedicine
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Neurosciences & Neurology
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Polymorphism, Single Nucleotide - Genetics
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Amyotrophic Lateral Sclerosis - Epidemiology
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C9Orf72 Protein
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Cacna1S
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