Zobrazeno 1 - 10
of 10
pro vyhledávání: '"A. F. Valiakhmetova"'
Autor:
A. F. Valiakhmetova, N. A. Mazerkina, L. I. Papusha, O. I. Bydanov, E. M. Tarasova, O. A. Medvedeva, N. K. Serova, L. A. Lazareva, L. V. Shishkina, Yu. Yu. Trunin, G. A. Novichkova, S. K. Gorelyshev, A. I. Karachunsky
Publikováno v:
Сибирский онкологический журнал, Vol 20, Iss 1, Pp 34-45 (2021)
Diencephalic cachexia (DC ) is a metabolic disorder characterized by a decrease in body weight. DC usually occurs in the presence of glioma brain tumors extended into the optic pathway. These tumors are very aggressive and have poor prognosis.Objecti
Externí odkaz:
https://doaj.org/article/7d1f3be056c647df8fc57c8ba1437f29
Autor:
L. I. Papusha, M. A. Zaytseva, A. V. Panferova, А. F. Valiakhmetova, K. A. Voronin, E. A. Salnikova, I. G. Vilesova, A. E. Druy, A. I. Karachunskiy, G. A. Novichkova
Publikováno v:
Pediatric Hematology/Oncology and Immunopathology. 21:12-18
Low grade gliomas (LGGs) are the most common brain tumors in children. Our retrospective-prospective study of biological characteristics of sporadic LGGs (not associated with neurofibromatosis type I) included 233 patients aged 0 to 18 years who had
Autor:
A. F. Valiakhmetova, L. I. Papusha, A. V. Sanakoeva, L. V. Shishkina, O. I. Budanov, G. A. Novichkova, S. K. Gorelyshev, A. I. Karachunskiy
Publikováno v:
Pediatric Hematology/Oncology and Immunopathology. 20:33-41
Choroid plexus tumors (CPTs) are rare intraventricular tumors, accounting 2–5% of brain tumors in children. Choroid plexus papilloma (CPP) classified by the World Health Organization (WHO) on the basis of histological criteria as benign tumor (WHO
Autor:
A. V. Sanakoeva, O.I. Bydanov, S. K. Gorelyshev, L V Shishkina, V.F. Voino-Yasenetsky Scientific, Immunology named after Dmitry Rogachev, Moscow, Russia, A.I. Karachunsky, A. F. Valiakhmetova, L. I. Papusha, G.A. Novichkova
Publikováno v:
Pediatria. Journal named after G.N. Speransky. 100:53-60
Choroid plexus tumors (CPT) are rare neoplasms accounting for 2–5% of all brain tumours in children, and are most commonly under 2 years of age. Most of these tumors present with symptoms of intracranial hypertension. Survival directly depends on t
Autor:
S. K. Gorelyshev, L. I. Papusha, A. V. Sanakoeva, O. I. Budanov, A. F. Valiakhmetova, A. I. Karachunskiy, L. V. Shishkina, G. A. Novichkova
Publikováno v:
Pediatric Hematology/Oncology and Immunopathology. 20:66-74
Choroid plexus carcinomas (CPCs) are rare pediatric tumors with a generally poor prognosis. Currently there is no definite optimal treatment strategy for this neoplasm. This study is supported by the Independent Ethics Committee and approved by the A
Publikováno v:
Uspehi Molekulârnoj Onkologii, Vol 7, Iss 3, Pp 37-47 (2020)
Background. High-grade gliomas are characterized by a wide range of genetic abnormalities. The heterogeneous genomic landscape of pediatric high-grade gliomas allows identifying distinct subgroups of the disease in children and young adults. Most imp
Autor:
L. A. Lasareva, L. V. Shiskina, Gorelyshev Sk, N A Mazerkina, N. K. Serova, O. A. Medvedeva, E. F. Valiakhmetova, Y. Y. Trunin, E. M. Tarasova
Publikováno v:
Pediatric Hematology/Oncology and Immunopathology. 18:28-38
Neurofibromatosis type I (NFI) is one of the most common brain tumor predisposition syndromes. Children with NFI are prone to develop a low grade gliomas, which can be localized in various areas of the brain, however, most of them occur in the struct
Publikováno v:
Uspehi Molekulârnoj Onkologii, Vol 6, Iss 2, Pp 28-41 (2019)
Low grade gliomas are the most common brain tumors in children. Total resection for operable lesion helps to achieve local and system control. Nevertheless, for inaccessible tumors are required more effective treatment both to overcome the refractory
Publikováno v:
Креативная хирургия и онкология, Vol 0, Iss 3, Pp 21-25 (2017)
92 patients with chronic anal fissure were treated depending on the cause of the disease and the magnitude of the basal pressure anal sphincter. It was found that, compared to the traditional method of surgical treatment, the use of “blind” stitc
Autor:
An. N. Konovalov, O. A. Medvedeva, Ozerova Vi, L A Satanin, E. F. Valiakhmetova, Khukhlaeva Ea, A. N. Savateev, Gorelyshev Sk, L V Shishkina
Publikováno v:
Voprosy neirokhirurgii imeni N.N. Burdenko. 80:66
Large parasagittal meningiomas, in particular hyperostotic ones, in children are rare and problematic in the differential diagnosis. The literature reports only single clinical cases related to this issue; opinions about the indications, surgical tre