Zobrazeno 1 - 10
of 46
pro vyhledávání: '"I M, Khidiyatova"'
Publikováno v:
Нервно-мышечные болезни, Vol 13, Iss 4 (2024)
Hereditary spastic paraplegias represent a group of hereditary neurodegenerative disorders predominantly affecting corticospinal tracts which manifest with prominent spasticity and reduced power in the muscles of the lower limbs. According to clinica
Externí odkaz:
https://doaj.org/article/568f8d2b099248af9ddfb98705cdd68f
Autor:
I. M. Khidiyatova, E. V. Saifullina, A. S. Karunas, A. F. Akhmetgaleyeva, R. F. Kutlubaeva, L. A. Smakova, S. L. Lobov, A. V. Polyakov, O. A. Shchagina, V. A. Kadnikova, O. P. Ryzhkova, R. V. Magzhanov, E. K. Khusnutdinova
Publikováno v:
Russian Journal of Genetics. 58:1145-1153
Autor:
A. F. Akhmetgaleyeva, R. F. Idrisova, E. K. Khusnutdinova, R. V. Magzhanov, E. V. Saifullina, V. V. Shavalieva, I. M. Khidiyatova, M. A. Yankina
Publikováno v:
Russian Journal of Genetics. 55:259-262
Hereditary spastic paraplegia (HSP) is a group of neurodegenerative disorders with a predominant lesion of the pyramidal tract. To date, mutations responsible for the disease have been identified in more than 70 genetic loci. The main causes of HSP d
Autor:
I. M. Khidiyatova, Gulnara Akhmadeeva, Anastasiya Petrova, Elza Khusnutdinova, Azamat Baitimerov, I. R. Gilyazova, R. V. Magzhanov
Publikováno v:
Neuroscience for Medicine and Psychology.
Publikováno v:
Neuroscience and Behavioral Physiology. 48:636-640
This review presents data from recent studies throughout the world on anxious-depressive disorders in patients with Parkinson’s disease (PD); their features and epidemiology are presented, along with details of pathogenesis, clinical properties, an
Autor:
Ancha Baranova, V. P. Puzyrev, Tatiana V. Tatarinova, N. N. Trofimova, Vadim Stepanov, Marina Gubina, Rita Khusainova, A. V. Marusin, Egor Prokhortchouk, Edward J. Vajda, A. B. Teslyuk, Oleg Balanovsky, Eugenia S. Boulygina, Maria Spiridonova, I. M. Khidiyatova, Alexandr M. Mazur, Martin Triska, Irina Khitrinskaya, Svetlana V. Tsygankova, Natalia A Konovalova, Ganesh Prasad Arun Kumar, Ekaterina Khrameeva, Petr Triska, Nikolay Chekanov, Konstantin Babalyan, V. L. Akhmetova, Sergey Litvinov, Elza Khusnutdinova, Konstantin G. Skryabin, V. N. Kharkov, D. Ivanoshchuk
Publikováno v:
BMC Genetics, Vol 18, Iss S1, Pp 5-20 (2017)
BMC Genetics
BMC Genetics
Background The history of human populations occupying the plains and mountain ridges separating Europe from Asia has been eventful, as these natural obstacles were crossed westward by multiple waves of Turkic and Uralic-speaking migrants as well as e
Autor:
Salavat Umutbaev, I. M. Khidiyatova, Gulnara Akhmadeeva, Azamat Baitimerov, I. R. Gilyazova, Rim Magjanov, Gulnaz N Tayupova
Publikováno v:
Journal of the Neurological Sciences. 429:119551
Autor:
Aliya Akhmetgaleyeva, Mariya Yankina, Rimma Idrisova, Elza Khusnutdinova, Elena Saifullina, I. M. Khidiyatova, R. V. Magzhanov
Publikováno v:
Neuroscience for Medicine and Psychology.
Autor:
R. V. Magzhanov, Elza Khusnutdinova, R. F. Idrisova, E. V. Saifullina, I. M. Khidiyatova, A. F. Akhmetgaleyeva
Publikováno v:
Russian Journal of Genetics. 52:603-607
Hereditary spastik paraplegias (HSP) are a group of neurodegenerative disorders with primary lesion of the pyramidal tract. The most frequent autosomal dominant form of the disease in Europeans is HSP associated with mutations in the spastin gene (SP
Autor:
E. Kh. Khusnutdinova, I. M. Khidiyatova, A. Kh. Nurgalieva, O. A. Kuramshina, A. Ya. Kryukova, E. Kh. Shaymardanova, F. R. Munasipov, L. V. Gabbasova, R. B. Sagitov
Publikováno v:
Russian Journal of Genetics. 52:320-330
Peptic ulcer disease is a chronic disease of the gastrointestinal tract, mainly manifesting itself in the formation of the fairly persistent ulcer defect of the mucous membrane of the stomach and/or duodenum. Association analysis of common polymorphi