Altynshash Jaxybayeva

Employment

• Astana Medical University Заведующая кафедрой неврологии
  2015 - Present

Education

Education history is unavailable.

Projects & Funding

Projects & funding information is unavailable.

Publications (18)

• Gene therapy in pediatric patients with spinal muscular atrophy in Kazakhstan: Challenges and achievements
  Pediatrics & Neonatology 2026 DOI: 10.1016/j.pedneo.2026.04.006
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• The prevalence of spinal muscular atrophy in Kazakhstan and the experience with the national nusinersen treatment program
  European Journal of Paediatric Neurology 2026 DOI: 10.1016/j.ejpn.2026.06.011
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• Elucidating the genomic basis of rare pediatric neurological diseases in Central Asia and Transcaucasia
  Nature Genetics 2024 DOI: 10.1038/S41588-024-02016-X
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• General movement assessment efficacy for assessment of nervous system integrity in children after hypoxic-ischemic encephalopathy in middle income countries
  Early Human Development 2024 DOI: 10.1016/j.earlhumdev.2024.105992
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• General movements assessment: A bibliometric analysis
  Early Human Development 2024 DOI: 10.1016/j.earlhumdev.2023.105924
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• SUBACUTE SCLEROSING PANENCEPHALITIS AS A CONSEQUENCE OF MEASLES INFECTION IN A CHILD IN EARLY CHILDHOOD (CLINICAL CASE): CURRENT FEATURES OF DIAGNOSIS, TREATMENT AND REHABILITATION IN KAZAKHSTAN
  Central Asian Medical Rehabilitation Bulletin 2024 DOI: 10.66684/3008-0606-2024-1-1-81-91
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• Duchenne Muscular Dystrophy in Kazakhstan: A Journey from Diagnosis to the Treatment, the Biases and Achievements
  Journal of Neuromuscular Diseases 2023 DOI: 10.3233/JND-221559
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• Preloaded combination nicotine replacement therapy for smoking cessation in Kazakhstan: A randomized controlled trial study protocol
  Plos One 2023 DOI: 10.1371/journal.pone.0292490
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• A review of diagnosis of Duchenne and Becker muscular dystrophy
  Journal of Clinical Medicine of Kazakhstan 2021 DOI: 10.23950/jcmk/11222
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• NTRK1 gene-related congenital insensitivity to pain with anhidrosis: a nationwide multicenter retrospective study
  Neurogenetics 2021 DOI: 10.1007/s10048-021-00668-z
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