Zobrazeno 1 - 10
of 207
pro vyhledávání: '"T-cell immunodeficiency"'
Autor:
Kensuke Nakagawara, Shotaro Chubachi, Shuhei Azekawa, Shiro Otake, Ayaka Saito, Masahiko Okada, Ko Lee, Katsunori Masaki, Naoyoshi Koike, Hirofumi Kamata, Ichiro Kawada, Shigeaki Suzuki, Makoto Ishii, Koichi Fukunaga
Publikováno v:
Respiratory Medicine Case Reports, Vol 33, Iss , Pp 101408- (2021)
Acquired immunodeficiency in thymoma (Good's syndrome) without hypogammaglobulinemia is a rare condition. Here we describe the case of a 29-year-old Japanese woman with thymoma-associated T cell immunodeficiency after radiation therapy. She was admit
Externí odkaz:
https://doaj.org/article/1c8bb0fae4c241a9820a444c8ef77473
Autor:
Janne Strand, Kiran Aftab Gul, Hans Christian Erichsen, Emma Lundman, Mona C. Berge, Anette K. Trømborg, Linda K. Sørgjerd, Mari Ytre-Arne, Silje Hogner, Ruth Halsne, Hege Junita Gaup, Liv T. Osnes, Grete A. B. Kro, Hanne S. Sorte, Lars Mørkrid, Alexander D. Rowe, Trine Tangeraas, Jens V. Jørgensen, Charlotte Alme, Trude E. H. Bjørndalen, Arild E. Rønnestad, Astri M. Lang, Terje Rootwelt, Jochen Buechner, Torstein Øverland, Tore G. Abrahamsen, Rolf D. Pettersen, Asbjørg Stray-Pedersen
Publikováno v:
Frontiers in Immunology, Vol 11 (2020)
Severe combined immunodeficiency (SCID) and other T cell lymphopenias can be detected during newborn screening (NBS) by measuring T cell receptor excision circles (TRECs) in dried blood spot (DBS) DNA. Second tier next generation sequencing (NGS) wit
Externí odkaz:
https://doaj.org/article/634d7c285f864c7781322eb1360b861b
Akademický článek
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Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 1997 Mar . 94(6), 2522-2527.
Externí odkaz:
https://www.jstor.org/stable/41671
Autor:
Georgios Sogkas, Natalia Dubrowinskaja, Anke K. Bergmann, Jana Lentes, Tim Ripperger, Mykola Fedchenko, Diana Ernst, Alexandra Jablonka, Robert Geffers, Ulrich Baumann, Reinhold E. Schmidt, Faranaz Atschekzei
Publikováno v:
Diseases, Vol 7, Iss 2, p 34 (2019)
Immunodeficiency, centromeric instability and facial anomalies syndrome 2 (ICF2) is a rare autosomal recessive primary immunodeficiency disorder. So far, 27 patients have been reported. Here, we present three siblings with ICF2 due to a homozygous ZB
Externí odkaz:
https://doaj.org/article/a72a40d7dffc448e9ddd0a156553ee78
Autor:
Katsunori Masaki, Hirofumi Kamata, Kensuke Nakagawara, Shuhei Azekawa, Koichi Fukunaga, Ichiro Kawada, Ayaka Saito, Naoyoshi Koike, Ko Lee, Shotaro Chubachi, Shiro Otake, Makoto Ishii, Shigeaki Suzuki, Masahiko Okada
Publikováno v:
Respiratory Medicine Case Reports, Vol 33, Iss, Pp 101408-(2021)
Respiratory Medicine Case Reports
Respiratory Medicine Case Reports
Acquired immunodeficiency in thymoma (Good's syndrome) without hypogammaglobulinemia is a rare condition. Here we describe the case of a 29-year-old Japanese woman with thymoma-associated T cell immunodeficiency after radiation therapy. She was admit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52de25f8704c1883d3ad1d76a13cd50b
http://www.sciencedirect.com/science/article/pii/S2213007121000708
http://www.sciencedirect.com/science/article/pii/S2213007121000708
Autor:
Olexander Hruzevskyi
Publikováno v:
The Austrian Journal of Technical and Natural Sciences. :14-21
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef64232c750ded851dce06152817e8fc
https://doi.org/10.29013/ajt-20-5.6-14-21
https://doi.org/10.29013/ajt-20-5.6-14-21
Autor:
Wei Loon Ng, Tem Lom Fam, Andy Sing Ong Tang, Qi Ying Wong, Pak Inn Teoh, Siaw Tze Yeo, Lee Ping Chew, Wei Huei Loh, Hock Hin Chua
Publikováno v:
The American journal of case reports. 22
BACKGROUND Good syndrome (thymoma with immunodeficiency) is a frequently missed and forgotten entity. It is a rare cause of combined B and T cell immunodeficiency in adults. To date, fewer than 200 patients with Good syndrome have been reported in th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::216106dedf67548c58ba26cb3a7df1a9
https://pubmed.ncbi.nlm.nih.gov/33712551
https://pubmed.ncbi.nlm.nih.gov/33712551
Autor:
Ulrich Baumann, Alexandra Jablonka, Reinhold E. Schmidt, Faranaz Atschekzei, Georgios Sogkas, Natalia Dubrowinskaja, Tim Ripperger, Jana Lentes, Diana Ernst, Mykola Fedchenko, Robert Geffers, Anke K. Bergmann
Publikováno v:
Diseases, Vol 7, Iss 2, p 34 (2019)
Diseases (Basel, Switzerland)
Diseases
Volume 7
Issue 2
Diseases (Basel, Switzerland)
Diseases
Volume 7
Issue 2
Immunodeficiency, centromeric instability and facial anomalies syndrome 2 (ICF2) is a rare autosomal recessive primary immunodeficiency disorder. So far, 27 patients have been reported. Here, we present three siblings with ICF2 due to a homozygous ZB
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62bbc52504d620f9bf9915d19d87767f
https://www.mdpi.com/2079-9721/7/2/34
https://www.mdpi.com/2079-9721/7/2/34
Autor:
Shuai Lu, Junyan Hu, Ling Xu, Bo Li, Yangqiu Li, Yankai Xiao, Chengwu Zeng, Lingling Zhou, Xu Wang
Publikováno v:
ImmunoTargets and Therapy. 7:77-81
Background T cell immunodeficiency is a common feature in patients with different kinds of hematological disease such as T cell non-Hodgkin lymphoma (T-NHL), B cells NHL (B-NHL), NK/T cell NHL (NK/T-CL) and acute myeloid leukemia (AML). In our recent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a7106a901596ae41a4774afcd46f8e8
https://doi.org/10.2147/itt.s179656
https://doi.org/10.2147/itt.s179656