Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Tat'yana S. Vargina"'
Autor:
Anna E. Pokrovskaya, Valery Podzolkov, Julia V. Lerner, Andrey B. Ponomarev, Yevgenia A. Kogan, Tat’yana S. Vargina
Publikováno v:
Case Reports in Gastroenterology, Vol 14, Iss 3, Pp 624-631 (2020)
Case Rep Gastroenterol
Case Rep Gastroenterol
Anaplastic pancreatic carcinoma is a very rare histological subtype of pancreatic cancer, which is characterized by a more aggressive course than for conventional ductal adenocarcinoma. In this article, we consider the features of the clinical course
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f69ca204574a8a24cbbb268a71b3118b
https://www.karger.com/Article/FullText/511037
https://www.karger.com/Article/FullText/511037
Publikováno v:
Case Reports in Oncology, Vol 11, Iss 3, Pp 814-821 (2018)
Case Reports in Oncology
Case Reports in Oncology
Introduction: Due to the beginning of the use of immunophenotypic and cytogenetic techniques, new nosological forms of lymphoproliferative diseases have appeared over the past few decades. According to the WHO classification (2008), today there are m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7eed5b4a9ea4b668afec30d85aa6b227
https://www.karger.com/Article/FullText/492665
https://www.karger.com/Article/FullText/492665
Autor:
V. I. Podzoklov, Tat’yana S. Vargina
Publikováno v:
Clinical Medicine (Russian Journal). 95:855-861
The authors discuss etiology, pathogenesis, and diagnostics of acute aortic syndrome characterized by the lesion of the aortic wall and report a case of this condition with a strikingly dramatic clinical picture with reference to its etiological caus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9e8b62d54aa32c2b7c23337ef0743848
https://doi.org/10.18821/0023-2149-2017-95-9-855-861
https://doi.org/10.18821/0023-2149-2017-95-9-855-861
Publikováno v:
Терапевтический архив, Vol 91, Iss 4, Pp 118-121 (2019)
Hereditary hemochromatosis (HH) is a disease with an autosomal recessive hereditary type, stipulated by the genetic defect that leads to a high intestinal absorption of iron and primary accumulation in the parenchymal cells of the liver and other org
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::945451344c74fbb6daebd324fb25b18f
https://pubmed.ncbi.nlm.nih.gov/31094485
https://pubmed.ncbi.nlm.nih.gov/31094485