Gulbahar H Bagyeva

Summary

Country: Russia

Publications

  1. ncbi Nikolai V. Konovalov (1900-1966): his role in the development of neurology and the creation of the Institute of Neurology of the Russian Academy of Medical Sciences
    Irina A Ivanova-Smolenskaya
    Institute of Neurology of the Russian Academy of Medical Sciences, Moscow, Russia
    J Hist Neurosci 16:160-7. 2007
  2. pmc Effective quantitative real-time polymerase chain reaction analysis of the parkin gene (PARK2) exon 1-12 dosage
    Maria I Shadrina
    Institute of Molecular Genetics, Russian Academy of Sciences, 2 Kurchatov Sq, 123182, Moscow, Russia
    BMC Med Genet 8:6. 2007
  3. ncbi Different phenotypes of Friedreich's ataxia within one 'pseudo-dominant' genealogy: relationships between trinucleotide (GAA) repeat lengths and clinical features
    S N Illarioshkin
    Department of Neurogenetics, Institute of Neurology, Russian Academy of Medical Sciences, Moscow, Russia
    Eur J Neurol 7:535-40. 2000
  4. ncbi Identical dysferlin mutation in limb-girdle muscular dystrophy type 2B and distal myopathy
    S N Illarioshkin
    Department of Neurogenetics, Institute of Neurology, Russian Academy of Medical Sciences, Moscow, Russia
    Neurology 55:1931-3. 2000

Collaborators

  • S N Illarioshkin
  • Irina A Ivanova-Smolenskaya
  • Maria I Shadrina
  • E D Markova
  • I A Ivanova-Smolenskaya
  • Sergei N Illarioshkin
  • Elena D Markova
  • Irina I Ivanova-Smolenskaia
  • Svetlana A Limborska
  • Elena V Semenova
  • Petr A Slominsky
  • Nikolai Konovalov
  • G K Bagieva
  • C R Greenberg
  • I V Ovchinnikov
  • K Wrogemann
  • S A Klyushnikov
  • V S Sukhorukov
  • V V Poleshchuk
  • E Nylen

Detail Information

Publications4

  1. ncbi Nikolai V. Konovalov (1900-1966): his role in the development of neurology and the creation of the Institute of Neurology of the Russian Academy of Medical Sciences
    Irina A Ivanova-Smolenskaya
    Institute of Neurology of the Russian Academy of Medical Sciences, Moscow, Russia
    J Hist Neurosci 16:160-7. 2007
    ....
  2. pmc Effective quantitative real-time polymerase chain reaction analysis of the parkin gene (PARK2) exon 1-12 dosage
    Maria I Shadrina
    Institute of Molecular Genetics, Russian Academy of Sciences, 2 Kurchatov Sq, 123182, Moscow, Russia
    BMC Med Genet 8:6. 2007
    ..Deletions and duplications of single exons or exon groups account for a large proportion of the gene mutations. Direct detection of these mutations can be used for the diagnosis of Parkinson's disease...
  3. ncbi Different phenotypes of Friedreich's ataxia within one 'pseudo-dominant' genealogy: relationships between trinucleotide (GAA) repeat lengths and clinical features
    S N Illarioshkin
    Department of Neurogenetics, Institute of Neurology, Russian Academy of Medical Sciences, Moscow, Russia
    Eur J Neurol 7:535-40. 2000
    ..Our observation clearly demonstrates the significance of variable-sized alleles for the phenotypic expression of the disease...
  4. ncbi Identical dysferlin mutation in limb-girdle muscular dystrophy type 2B and distal myopathy
    S N Illarioshkin
    Department of Neurogenetics, Institute of Neurology, Russian Academy of Medical Sciences, Moscow, Russia
    Neurology 55:1931-3. 2000
    ..This finding supports the view that additional factors (e.g., modifier genes) contribute to the phenotypic expression of causative mutations in dysferlinopathies...