Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Talgat Khaibullin"'
Autor:
Saltanat Abdraimova, Zhanybek Myrzayev, Altynay Karimova, Altynay Talgatkyzy, Talgat Khaibullin, Gulnaz Kaishibayeva, Sandugash Elubaeva, Karlygash Esembekova, Dongrak Choi, Pablo Martinez-Martin, Christopher G. Goetz, Glenn T. Stebbins, Sheng Luo, Chingiz Shashkin, Nazira Zharkinbekova, Rauan Kaiyrzhanov
Publikováno v:
Clinical Parkinsonism & Related Disorders, Vol 10, Iss , Pp 100232- (2024)
Background and Purpose: The International Movement Disorder Society revision of the Unified Parkinson’s Disease Rating Scale (MDS-UPDRS) is widely used in the assessment of the severity of Parkinson’s disease (PD). This study aimed to validate th
Externí odkaz:
https://doaj.org/article/496a5217de4d4eaa9b12774c741e89d4
Autor:
Rauan Kaiyrzhanov, Akbota Aitkulova, Jana Vandrovcova, David Murphy, Nazira Zharkinbekova, Chingiz Shashkin, Vadim Akhmetzhanov, Gulnaz Kaishibayeva, Altynay Karimova, Zhanybek Myrzayev, Malgorzata Murray, Talgat Khaibullin, John Hardy, Henry Houlden
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 6, Pp n/a-n/a (2021)
ABSTRACT Background Knowledge of the genetic background of many human diseases is currently lacking from genetically undiscovered regions, including Central Asia. Kazakhstan is the first Central Asian country where the genetic studies of Parkinson's
Externí odkaz:
https://doaj.org/article/cad4a07db35648faade6d7016496b8e2
Autor:
Rauan Kaiyrzhanov, Akbota Aitkulova, Chingiz Shashkin, Nazira Zharkinbekova, Mie Rizig, Elena Zholdybayeva, Zharkyn Jarmukhanov, Vadim Akhmetzhanov, Gulnaz Kaishibayeva, Talgat Khaibullin, Altynay Karimova, Serik Akshulakov, Askhat Bralov, Nurlan Kissamedenov, Zhanar Seidinova, Anjela Taskinbayeva, Aliya Muratbaikyzy, Henry Houlden
Publikováno v:
Parkinson's Disease, Vol 2020 (2020)
Background. LRRK2 mutations have emerged as the most prevalent and potentially treatable determinants of Parkinson’s disease (PD). Peculiar geographic distribution of these mutations has triggered an interest in genotyping PD cohorts of different e
Externí odkaz:
https://doaj.org/article/e1290314fb6d4c18a782d814d7b74bc4
Autor:
Rauan Kaiyrzhanov, Mie Rizig, Akbota Aitkulova, Nazira Zharkinbekova, Chingiz Shashkin, Gulnaz Kaishibayeva, Altynay Karimova, Talgat Khaibullin, Dinara Sadykova, Manizha Ganieva, Khurshidakhon Rasulova, Henry Houlden
Publikováno v:
Parkinson's Disease, Vol 2019 (2019)
Our understanding of Parkinson’s disease (PD) has significantly accelerated over the last few years, but predominant advances have been made in developed, Western countries. Little is known about PD in the Central Asian (CA) and Transcaucasian (TC)
Externí odkaz:
https://doaj.org/article/e3f28fd22b6a4a5aa21ba47e3b83688a
Autor:
Natalya Glushkova, Oksana Yurkovskaya, Antonio Sarría-Santamera, Idaliya Rakhimova, Tair Nurpeissov, Galiya Alikeyeva, Lyudmila Pivina, Zhanar Abdrakhmanova, Talgat Khaibullin, Yelena Ainabekova, Ayan Abdrakhmanov, Yuliya Semenova, Vitalii Kovalchuk
Publikováno v:
Radiation and Environmental Biophysics. 61:17-28
The issue of radiation exposure as a potential cause of cerebrovascular disease raises many concerns. The aim of the present study was to investigate the epidemiology of stroke and transient ischemic attacks (TIA) along with the associated risk facto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc26a700178799c4b49012704168175d
https://doi.org/10.1007/s00411-021-00955-1
https://doi.org/10.1007/s00411-021-00955-1
Autor:
Zhanar Urazalina, Yerbol Smail, Talgat Khaibullin, Vitalii Koval`chuk, Ayan Abdrakhmanov, Idaliya Rakhimova
Publikováno v:
Open Access Macedonian Journal of Medical Sciences. 9:170-173
BACKGROUND: Patients with heart failure (HF) and implanted heart devices constitute a vulnerable category during the coronavirus disease –2019 (COVID-19) pandemic. The remote monitoring function allows the physician to detect atrial fibrillation (A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::72274f56529f05cd1377a591bbf7d54a
https://doi.org/10.3889/oamjms.2021.6687
https://doi.org/10.3889/oamjms.2021.6687
Autor:
Nurlan Kissamedenov, Serik Akshulakov, Vadim Akhmetzhanov, Henry Houlden, Chingiz Shashkin, Talgat Khaibullin, Altynay Karimova, Rauan Kaiyrzhanov, Zharkyn Jarmukhanov, Askhat Bralov, Anjela Taskinbayeva, Gulnaz Kaishibayeva, Aliya Muratbaikyzy, Zhanar Seidinova, Nazira Zharkinbekova, Akbota Aitkulova, Mie Rizig, Elena Zholdybayeva
Publikováno v:
Parkinson's Disease
Parkinson's Disease, Vol 2020 (2020)
Parkinson's Disease, Vol 2020 (2020)
Background. LRRK2 mutations have emerged as the most prevalent and potentially treatable determinants of Parkinson’s disease (PD). Peculiar geographic distribution of these mutations has triggered an interest in genotyping PD cohorts of different e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60fc9ddb47ac0919a6143644aa3fbde2
https://doi.org/10.1155/2020/2763838
https://doi.org/10.1155/2020/2763838
Autor:
Idaliya Rakhimova, Yuliya Semenova, Talgat Khaibullin, Anargul Kuanysheva, Vitalii Kovalchuk, Ayan Abdrakhmanov
Publikováno v:
Current cardiology reviews. 18(4)
Background: Stroke is a problem worldwide because of its high mortality and disability rates. Almost 90% of strokes are ischemic, and more than half of the deaths are caused by an ischemic stroke. Most risk factors for stroke are manageable so that i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b96cf01890e6661ccc0ee634fe4cae2d
https://pubmed.ncbi.nlm.nih.gov/34939547
https://pubmed.ncbi.nlm.nih.gov/34939547
Autor:
Henry Houlden, Gulnaz Kaishibayeva, Talgat Khaibullin, John Hardy, Nazira Zharkinbekova, Akbota Aitkulova, Zhanybek Myrzayev, Chingiz Shashkin, Jana Vandrovcova, David Murphy, Altynay Karimova, Rauan Kaiyrzhanov, Malgorzata Murray, Vadim Akhmetzhanov
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 6, Pp n/a-n/a (2021)
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine
Background Knowledge of the genetic background of many human diseases is currently lacking from genetically undiscovered regions, including Central Asia. Kazakhstan is the first Central Asian country where the genetic studies of Parkinson's disease (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9e7200e64dc5176d2f78025f4ed3a93
https://doaj.org/article/cad4a07db35648faade6d7016496b8e2
https://doaj.org/article/cad4a07db35648faade6d7016496b8e2
Autor:
Rauan Kaiyrzhanov, Talgat Khaibullin, Nazira Zharkinbekova, Mie Rizig, Chingiz Shashkin, Dinara Z. Sadykova, Henry Houlden, Zhanar Seidinova, Altynay Karimova, Anjela Taskinbayeva, Gulnaz Kaishibayeva, Vadim Akhmetzhanov
Publikováno v:
Journal of Parkinson's Disease
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3bc67970f41099e321314afe052ece6
https://doi.org/10.3233/jpd-191782
https://doi.org/10.3233/jpd-191782