Zobrazeno 1 - 10
of 249
pro vyhledávání: '"hereditary predisposition"'
Publikováno v:
Терапевтический архив, Vol 96, Iss 2, Pp 159-167 (2024)
Irritable bowel syndrome (IBS) is one of the most common diseases of the digestive tract from the group of disorders of interaction in the gut-brain axis. IBS has a negative impact of on patients' quality of life and the significant social and econom
Externí odkaz:
https://doaj.org/article/1de39fb4c41e42e78ca37b3f08877475
Publikováno v:
Dermatology Practical & Conceptual, Vol 14, Iss 3 (2024)
Externí odkaz:
https://doaj.org/article/3c4e7cceb8954cbeb6b62d37cc3cfedd
Hereditary predisposition of water voles (Arvicola amphibius L.) to seizures in response to handling
Autor:
G. G. Nazarova, L. P. Proskurnyak
Publikováno v:
Вавиловский журнал генетики и селекции, Vol 26, Iss 4, Pp 371-377 (2022)
Finding out the hereditary predisposition to seizures in response to specific external stimuli is important for understanding the causes of epileptiform conditions, developing new methods for their prevention and therapies. In the water vole, individ
Externí odkaz:
https://doaj.org/article/6dfbded00a4e407da4f6a487332c1b8f
Publikováno v:
Frontiers in Oncology, Vol 13 (2023)
The pathogenesis of acute leukemia is still complex and vague. Most types of acute leukemia are related to somatic gene mutations, and familial incidence is rare. Here we report a case of familial leukemia. The proband presented to our hospital with
Externí odkaz:
https://doaj.org/article/4e5bd46af29e4d5e9ce81444a3e88046
Autor:
Anjum B. Khan, David Bowen
Publikováno v:
Hemato, Vol 3, Iss 1, Pp 17-37 (2021)
Myelodysplastic syndromes affect an older age group with a median age at onset in the eighth decade of life. As such, there is a relationship between the pathogenesis of MDS and age-related processes affecting haematopoietic stem/progenitor cells and
Externí odkaz:
https://doaj.org/article/42b2c7f3938843d1b1a840f5a590304a
Autor:
A. M. Zhumakayev, V. V. Benberin, N. A. Shanazarov, M. E. Tuleutaev, N. K. Seydalin, A. Zh. Davranov, A. M. Zhumakayeva, T. M. Muratov, B. G. Kasymov
Publikováno v:
Сибирский онкологический журнал, Vol 20, Iss 5, Pp 162-169 (2021)
Purpose of the study: to present up-to-date data on molecular genetic studies aimed to identify the risks of developing prostate cancer in representatives of various ethnic groups. Material and Methods. Literary sources were searched in databases suc
Externí odkaz:
https://doaj.org/article/9e7ba971b1e140d984c2785c41597b52
Akademický článek
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Autor:
Kseniia I. Zarubina, Elena N. Parovichnikova, Vadim L. Surin, Olesia S. Pshenichnikova, Olga A. Gavrilina, Galina A. Isinova, Vera V. Troitskaya, Andrei N. Sokolov, Irina V. Galtseva, Nikolai M. Kapranov, Juliia O. Davydova, Tatiana N. Obukhova, Elena E. Nikulina, Andrei B. Sudarikov, Valerii G. Savchenko
Publikováno v:
Терапевтический архив, Vol 93, Iss 7, Pp 763-769 (2021)
Background. LiFraumeni syndrome (LFS) is a rare, autosomal dominant, hereditary disorder that is characterized by an increased risk for certain types of cancer, acute lymphoblastic leukemia (ALL), particularly. Germline TP53 mutations are associated
Externí odkaz:
https://doaj.org/article/4563d78ac8784404906e76a3496b7a84
Publikováno v:
Сибирский научный медицинский журнал, Vol 40, Iss 5, Pp 113-121 (2020)
The aim is to study the prevalence of gastroesophageal reflux disease (GERD), gastroduodenal erosions and ulcers and their association with a family predisposition for ulcer disease in Siberian schoolchildren. Material and methods. We have examined s
Externí odkaz:
https://doaj.org/article/8911593a59144f8abbef388bb6b9b5cc
Autor:
A. V. Morkovina, E. Yu. Yuryeva, T. L. Lapina, P. V. Pavlov, A. S. Tertychnyy, A. A. Sheptulin
Publikováno v:
Сеченовский вестник, Vol 11, Iss 3, Pp 70-77 (2020)
Hereditary predisposition is the most significant risk factor for Crohn’s disease (CD) in siblings. Case reports. CD was diagnosed in 3 brothers in a family with 6 children of the same generation: the disease manifested itself in one — at the age
Externí odkaz:
https://doaj.org/article/e8cd221bf80d4dd49e44185c7aa0e2d4