Showing 1 - 4 results of 4 for search 'I. A. Akimova' Skip to content
    • About the Library
    • Rules and Regulations
    • Library Services
    • Library Hours
  • Library News
    • Digital Repository
    • Google Scholar
    • ResearchGate
    • AJoGPL
    • KURJ
    • AJLS
    • MyLOFT
    • Lexis Plus UK
    • Britannica Academic
    • Research Support Tools
    • Quick Resource Links
  • Login
Advanced
  • Author
  • I. A. Akimova
Showing 1 - 4 results of 4 for search 'I. A. Akimova', query time: 0.02s Refine Results
  1. 1
    Clinical and genetic characteristics and diagnosis of hereditary variants of neonatal epilepsy

    Clinical and genetic characteristics and diagnosis of hereditary variants of neonatal epilepsy by N. A. Semenova, E. L. Dadali, A. A. Sharkov, I. A. Akimova

    Published 2017-11-01
    Get full text
    Article
    Save to List
    Saved in:
  2. 2
    HEREDITARY DISEASES AND SYNDROMES ACCOMPANIED BY FEBRILE CONVULSIONS: CLINICAL AND GENETIC CHARACTERISTICS AND DIAGNOSTIC PROCEDURES

    HEREDITARY DISEASES AND SYNDROMES ACCOMPANIED BY FEBRILE CONVULSIONS: CLINICAL AND GENETIC CHARACTERISTICS AND DIAGNOSTIC PROCEDURES by E. L. Dadali, A. A. Sharkov, I. V. Sharkova, I. V. Kanivets, F. A. Konovalov, I. A. Akimova

    Published 2016-08-01
    Get full text
    Article
    Save to List
    Saved in:
  3. 3
    Early epileptic encephalopathy associated with SCN2A mutations: clinical and genetic description of eight novel patients

    Early epileptic encephalopathy associated with SCN2A mutations: clinical and genetic description of eight novel patients by E. L. Dadali, F. A. Konovalov, I. A. Akimova, A. A. Sharkov, G. E. Rudenskaya, S. V. Mikhaylova, S. A. Korostelev

    Published 2018-07-01
    Get full text
    Article
    Save to List
    Saved in:
  4. 4
    Clinical and genetic characteristics of patients with type 2 early infantile epileptic encephalopathy caused by CDKL5 gene mutations

    Clinical and genetic characteristics of patients with type 2 early infantile epileptic encephalopathy caused by CDKL5 gene mutations by E. L. Dadali, I. A. Akimova, F. A. Konovalov, P. A. Shatalov, A. Yu. Krasnenko, V. V. Strelnikov, M. A. Ampleeva

    Published 2020-01-01
    Get full text
    Article
    Save to List
    Saved in:

Search Tools:

  • RSS Feed
  • Email Search

Search Options

  • Search History
  • Advanced Search

Find More

  • Browse the Catalog
  • Explore Channels
  • Course Reserves
  • New Items

Need Help?

  • Search Tips
  • Ask a Librarian
  • FAQs