Zobrazeno 1 - 10
of 17
pro vyhledávání: '"D V Rogozhin"'
Autor:
N. E. Kushlinskii, O. V. Kovaleva, Yu. B. Kuzmin, E. V. Samoilova, P. L. Prishchep, E. S. Gershtein, S. R. Varfolomeeva, D. V. Rogozhin, N. Yu. Sokolov, K. A. Borzov, E. A. Sushentsov, A. K. Valiev, I. S. Stilidy
Publikováno v:
Успехи молекулярной онкологии, Vol 10, Iss 2, Pp 100-107 (2023)
Introduction. Enzyme-linked immunosorbent assay of biochemical markers is one of the most important methods for diagnosing tumors. One of these markers is an inducer of expression of matrix metalloproteases EMMPRIN/CD147. Changes in its expression ar
Externí odkaz:
https://doaj.org/article/e5a5401085ba4e098a71e484a7840114
Publikováno v:
Опухоли головы и шеи, Vol 8, Iss 3, Pp 12-20 (2018)
The study objective is to determine the clinical and radiological characteristics of fibrous dysplasia of the maxillofacial area in children.Materials and methods. A retrospective analysis of the data of the Department of Maxillofacial Surgery of the
Externí odkaz:
https://doaj.org/article/018c03b705d54db78d0da5b3debddb4a
Autor:
A. V. Lopatin, A. Yu. Kugushev, N. S. Grachev, S. A. Yasonov, N. I. Ponomareva, D. V. Rogozhin, A. V. Pshonkin
Publikováno v:
Pediatric Hematology/Oncology and Immunopathology. 20:168-177
Melanotic neuroectodermal tumor of infancy is a rare neoplasm that predominantly involves cranial bones and tends to occur during the first year of life. About 500 cases have been described in the literature to date; 6% of them have been reported to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ec058ab1475a29240d0633a9877461fb
https://doi.org/10.24287/1726-1708-2021-20-4-168-177
https://doi.org/10.24287/1726-1708-2021-20-4-168-177
Autor:
D. V. Rogozhin, A. P. Shekhtman
Publikováno v:
Bone and soft tissue sarcomas, tumors of the skin. 13:32-40
Cranial chondroid tumors are a large group of benign and malignant neoplasms. The histological diagnosis plays a crucial role for treatment of patients with this pathology, especially, for cases of tumors with uncertain malignancy such as atypical ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ccd9f13faafe3bdc1e77da537db55b49
https://doi.org/10.17650/2070-9781-2021-13-1-32-40
https://doi.org/10.17650/2070-9781-2021-13-1-32-40
Autor:
D. S. Abramov, D. M. Konovalov, D. V. Rogozhin, N. V. Myakova, E. R. Biyachuev, V. Yu. Roshchin, A. M. Mitrofanova, A. N. Kislyakov
Publikováno v:
Онкогематология, Vol 8, Iss 2, Pp 34-40 (2014)
Subcutaneous panniculitis-like T-cell lymphoma (SPTL) is a rare tumor from αβ mature cytotoxic T-lymphocytes, which primarily affects the subcutaneous adipose tissue and has morphological manifestations similar to panniculitis. SPTL frequency is le
Externí odkaz:
https://doaj.org/article/bd6d6e62b3854ee9b67c7c1dbc3a8f08
Publikováno v:
Опухоли головы и шеи, Vol 0, Iss 4, Pp 30-31 (2015)
The paper proposed a procedure that can prevent peristomal recurrences in patients with larynx cancer after laryngectomy (LE). In the period 2010 to 2011, LE was performed in 95 patients with III stage T3N0M0 larynx cancer (according to the conventio
Externí odkaz:
https://doaj.org/article/bdda4c30ab6145bd8ff611666cb98bce
Publikováno v:
Russian Journal of Pediatric Surgery. 22:179-182
Fibrous dysplasia is a benign hamartoma bone disease, characterized by a combination of fibrous bone elements in the area of the focus. In the last 15 years, there has been a tendency to expand indications for the surgical treatment and the volume of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e5f711284ca5a0f1088f07a622fa9f82
https://doi.org/10.18821/1560-9510-2018-22-4-179-182
https://doi.org/10.18821/1560-9510-2018-22-4-179-182
Publikováno v:
Voprosy gematologii/onkologii i immunopatologii v pediatrii. 16:33-39
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::33e64676b6ecbb375b167fb4e0226ee2
https://doi.org/10.24287/1726-1708-2017-16-2-33-39
https://doi.org/10.24287/1726-1708-2017-16-2-33-39
Publikováno v:
Arkhiv patologii. 79(3)
Extrarenal extracranial rhabdoid tumor (EERT) is a rare malignant pediatric tumor characterized by extremely aggressive behavior, rapid metastatic spread, low survival rates, and no targeted therapy. The morphological diagnosis of classical cases of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b67bfd1c9620a19f028ed4983322ecd
https://pubmed.ncbi.nlm.nih.gov/28631714
https://pubmed.ncbi.nlm.nih.gov/28631714
Publikováno v:
Arkhiv patologii. 78:36
Non-ossifying fibroma (NOF) or metaphyseal fibrous defect (MFD) is benign fibroblast proliferation with the presence of osteoclast-like multinucleated giant cells. The most cases of NOF/MFD occur in the metaphysis of the long tubular bones of the low
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb5c12c01e5497ccbcde17beef19308d
https://doi.org/10.17116/patol201678236-40
https://doi.org/10.17116/patol201678236-40