Zobrazeno 1 - 10
of 64
pro vyhledávání: '"immunodeficiency, primary"'
Autor:
Guy Bader, Michal Itan, Liat Edry-Botzer, Hadar Cohen, Orly Haskin, Yael Mozer-Glassberg, Liora Harel, Ariel Munitz, Nufar Marcus Mandelblit, Motti Gerlic
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
Protective immunity against COVID-19 is orchestrated by an intricate network of innate and adaptive anti-viral immune responses. Several vaccines have been rapidly developed to combat the destructive effects of COVID-19, which initiate an immunologic
Externí odkaz:
https://doaj.org/article/6ff60f72677c496c936b6e9922607b2c
Autor:
Lauren J. Howson, Vanessa L. Bryant
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
Externí odkaz:
https://doaj.org/article/3513781b63ea40d89c23693dfcc225a3
Autor:
Zhongdong Lv, Yong Chen, Houqing Zhou, Zhonglin Chen, Qianru Yao, Jiali Ren, Xianglu Liu, Shuang Liu, Xiaomei Deng, Yingchen Pang, Weijun Chen, Huiling Yang, Ping Xu
Publikováno v:
Frontiers in Cellular and Infection Microbiology, Vol 12 (2022)
Whipple’s disease is a rare chronic systemic disease that affects almost any organ system of the body caused by the intracellular bacterium Tropheryma whipplei, which is found ubiquitously in the environment. Sequencing of the T. whipplei genome ha
Externí odkaz:
https://doaj.org/article/1f850c39a61b4d87bb78502154ef0975
Autor:
Aleksandra Szczawińska-Popłonyk, Elzbieta Grześk, Eyal Schwartzmann, Anna Materna-Kiryluk, Jadwiga Małdyk
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Autoimmune lymphoproliferative syndrome (ALPS) is a disorder characterized by a disruption of the lymphocyte apoptosis pathway, self-tolerance, and immune system homeostasis. Defects in genes within the first apoptosis signal (FAS)-mediated pathway c
Externí odkaz:
https://doaj.org/article/e3aee73dec1541c7a6c6cf5df7ebf0ff
Autor:
Evelien G. G. Sprenkeler, Carla Guenther, Imrul Faisal, Taco W. Kuijpers, Susanna C. Fagerholm
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
Megakaryoblastic leukemia 1 (MKL1) deficiency is one of the most recently discovered primary immunodeficiencies (PIDs) caused by cytoskeletal abnormalities. These immunological “actinopathies” primarily affect hematopoietic cells, resulting in de
Externí odkaz:
https://doaj.org/article/07ffcb7a7ba6477aad0e98154ba2571c
Autor:
Puja Sood Rajani, Maria A. Slack
Publikováno v:
Frontiers in Pediatrics, Vol 6 (2019)
Here we describe two term male infants diagnosed with X-linked CGD who present, in addition to frequent infection, with a unique papulopustular skin rash. CGD is caused by a number of genetic defects that impair phagocyte function. This disease resul
Externí odkaz:
https://doaj.org/article/49bbb880946c4eea837821a671c76a05
Akademický článek
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Akademický článek
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Publikováno v:
Sultan Qaboos University Medical Journal, Vol 7, Iss 2, Pp 133-138 (2007)
Over the last 17 years different forms of severe combined immunodeficiency have been diagnosed at Sultan Qaboos University Hospital, Muscat. Omenn’s syndrome is a rare autosomal recessive form of severe combined immunodeficiency. We report a 6 week
Externí odkaz:
https://doaj.org/article/42f78c7433b440b2bfd5bebd1af5b19b
Publikováno v:
Frontiers in immunology. 12
Megakaryoblastic leukemia 1 (MKL1) deficiency is one of the most recently discovered primary immunodeficiencies (PIDs) caused by cytoskeletal abnormalities. These immunological “actinopathies” primarily affect hematopoietic cells, resulting in de