Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Acquired Agammaglobulinemia"'
Autor:
O. Forssman, B. Herner
Publikováno v:
Acta Medica Scandinavica. 176:779-786
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d324cba51142e6769d646f2b44981b74
https://doi.org/10.1111/j.0954-6820.1964.tb00688.x
https://doi.org/10.1111/j.0954-6820.1964.tb00688.x
Akademický článek
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Autor:
Yutaka ISHIDA, Katsuhide ENSAKO, Takahiro TAMURA, Hideo ONODERA, Tadashi OFUJI, Junta KAMURA, Hazime SATO
Publikováno v:
Nihon Naika Gakkai Zasshi. 64:127-135
原発性免疫不全症の分類は未だ確立されていないが,われわれは,いわゆるprimary acquired agammaglobulinemia, WHOの分類試案ではvariable immunodeficiencyに属すると思われる24才の女性症例を経験したの
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c288562e30b97bf8f4827ab65ca2c33e
https://doi.org/10.2169/naika.64.127
https://doi.org/10.2169/naika.64.127
Publikováno v:
Nihon Naika Gakkai Zasshi. 63:49-56
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aec277400ade3176e2ac4095f51f1273
https://doi.org/10.2169/naika.63.49
https://doi.org/10.2169/naika.63.49
Publikováno v:
New England Journal of Medicine. 293:62-65
Three males in one family (two siblings and one maternal cousin) had an illness with cervical adenopathy, hepatosplenomegaly, and a fulminant febrile course. In the two survivors agammaglobulinemia developed. One of them became ill at the age of six
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d2f13c79ae3c290d1d6709615424dff
https://doi.org/10.1056/nejm197507102930202
https://doi.org/10.1056/nejm197507102930202
Autor:
Nobuhiro Sakaki, Susumu Kawamura, Shoshi Matsuda, Daizo Kan, Kiwamu Okita, Mikio Nishioka, Harushige Furutani, Tadayoshi Takemoto, Mitsuru Odawara, Shigemi Ariyama
Publikováno v:
Nihon Naika Gakkai Zasshi. 68:548-558
原発性後天性無γ-globulin血症, WHOの分類試案ではvariable common immunodeficiencyに属するとおもわれる33才の男性症例を経験したので報告する.患者は乳幼児期に麻疹,流行性耳下腺炎に罹患したが
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::13b26c57d027c39fe5c3d4ee05980259
https://doi.org/10.2169/naika.68.548
https://doi.org/10.2169/naika.68.548
Publikováno v:
Journal of Clinical Immunology. 1:94-100
Coculture experiments between lymphocytes of a 17-year-old immunodeficient male, DL, and a group of normal subjects, assaying pokeweed mitogen (PWM)-stimulated Ig secretion as a measure of B-cell function, revealed immunoregulatory abnormalities. Ini
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0f61e2b1d8071e60a9d2beed3fb943f
https://doi.org/10.1007/bf00915385
https://doi.org/10.1007/bf00915385
Publikováno v:
Clinical Immunology and Immunopathology. 20:57-62
The correspondence between the Fc markers and the TH 2 − markers on T cells was studied utilizing an autoantibody to a TH 2 − T-cell subset. This antibody was obtained from a patient with acquired agammaglobulinemia. Lymphocytotoxicity studies an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1a7d095ec713f2e8de049b11d1e1b11
https://doi.org/10.1016/0090-1229(81)90162-8
https://doi.org/10.1016/0090-1229(81)90162-8
Publikováno v:
Proceedings of the National Academy of Sciences. 60:881-885
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df741fbe4508ed70ddcf91083599f6f8
https://doi.org/10.1073/pnas.60.3.881
https://doi.org/10.1073/pnas.60.3.881
Autor:
John K. Wolf
Publikováno v:
New England Journal of Medicine. 266:473-480
PRIMARY agammaglobulinemia was once thought to be an extremely rare condition. However, since Bruton1 first recognized the syndrome in 1952, nearly 200 cases have appeared in the literature. These fall into three pathological categories: primary cong
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5c23c04b2eba33133c97ed0b35ff861
https://doi.org/10.1056/nejm196203082661001
https://doi.org/10.1056/nejm196203082661001