Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Sh. M. Safin"'
Publikováno v:
Неврология, нейропсихиатрия, психосоматика, Vol 11, Iss 3, Pp 74-77 (2019)
Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome (CANVAS) is a slowly progressive ataxic disorder characterized by the triad of cerebellar impairment, bilateral vestibular hypofunction, and sensory polyneuropathy. The pap
Externí odkaz:
https://doaj.org/article/340bcff81da24899ba1d36b6228db3d5
Publikováno v:
Креативная хирургия и онкология, Vol 9, Iss 3, Pp 234-238 (2019)
Introduction. Glioblastoma multiforme (GBM) is the most common and aggressive form of primary malignant brain tumour in adults associated with a poor prognosis. Exosomes have been shown to be useful non-invasive biomarkers for the diagnosis and progn
Externí odkaz:
https://doaj.org/article/0c4a2de2db3845288b411c33d4683378
Publikováno v:
Vestnik nevrologii, psihiatrii i nejrohirurgii (Bulletin of Neurology, Psychiatry and Neurosurgery). :15-19
Chiari malformation in the onset of the disease can manifest itself in a different clinical symptom complex. The literature describes isolated cases of a combination of Chiari malformation with hearing impairment. The article presents a description o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6e534928e96493865a7c73f416288229
https://doi.org/10.33920/med-01-2010-02
https://doi.org/10.33920/med-01-2010-02
Publikováno v:
Vestnik nevrologii, psihiatrii i nejrohirurgii (Bulletin of Neurology, Psychiatry and Neurosurgery). :25-33
Relevance. The study of the genetic mechanisms of the Chiari malformation is based on the study of genes of a possible predisposition to this pathology in combination with environmental factors that form the pathogenetic chain of the disease. Objecti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9707e8c596eb275e58edb6713be23216
https://doi.org/10.33920/med-01-2005-03
https://doi.org/10.33920/med-01-2005-03
Publikováno v:
Zhurnal nevrologii i psikhiatrii im. S.S. Korsakova. 121:110
Progressive supranuclear palsy (PNP) is a neurodegenerative disease characterized by a combination of progressive akinetic-rigid syndrome, postural instability with frequent falls, supranuclear ophthalmoplegia, pseudobulbar syndrome and frontal demen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10403768838e33b3531eb958e2d38e99
https://doi.org/10.17116/jnevro2021121031110
https://doi.org/10.17116/jnevro2021121031110
Autor:
N. M. Blinova, Sh. M. Safin, M. A. Kutlubaev, O. G. Afanasyeva, B. A. Bakirov, H. P. Derevyanko
Publikováno v:
Voprosy neirokhirurgii imeni N.N. Burdenko. 84:118
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0e492a3c9ffdf0c43da483c337fcbdf7
https://doi.org/10.17116/neiro202084011118
https://doi.org/10.17116/neiro202084011118
Autor:
I F Gareev, Sh. M. Safin
Publikováno v:
Voprosy neirokhirurgii imeni N.N. Burdenko. 83:112
Cerebral aneurysms are characterized by pathological expansion and thinning of the wall of vessels on the brain base, which may lead to rupture and subarachnoid hemorrhage (SAH) that is a life-threatening condition. This dictates the need for identif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3aaa1df1f1f015ab8ce9e7a6e79e914
https://doi.org/10.17116/neiro201983011112
https://doi.org/10.17116/neiro201983011112
Autor:
V. I. Manashchuk, Sh. M. Safin, V. E. Parfenov, O. A. Perl’mutter, N. A. Konovalov, V. V. Rerikh, Krylov Vv, M. N. Kravtsov, V. A. Manukovskii, A. A. Grin, A. K. Dulaev, A. A. Lutsik
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41f4d1b0e2a0215aea0f920e70c7d1e2
https://pubmed.ncbi.nlm.nih.gov/25909749
https://pubmed.ncbi.nlm.nih.gov/25909749
Autor:
V. I. Manashchuk, A. A. Lutsyk, Sh. M. Safin, V. E. Parfenov, Krylov Vv, A. K. Dulaev, O. A. Perl’mutter, M. N. Kravtsov, A. A. Grin, V. V. Rerikh, V. A. Manukovskiy, N. A. Konovalov
Publikováno v:
Scopus-Elsevier
Europe PubMed Central
Europe PubMed Central
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6cfd669e1835584f39433fd61faeb9e8
https://doi.org/10.17116/neiro201579297-110
https://doi.org/10.17116/neiro201579297-110
Publikováno v:
Voprosy meditsinskoi khimii. 38(1)
Excretion of glycosaminoglycans (GAG) with urine was 2.7-fold decreased in patients with syringomyelia as compared with healthy persons. Patterns of GAG decreased excretion are genetically determined and inherited as dominant features. Content of GAG
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ad4cf6a5813e3869bd799f57cab28c39
https://pubmed.ncbi.nlm.nih.gov/1441283
https://pubmed.ncbi.nlm.nih.gov/1441283