Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Bruton disease"'
Autor:
S. V. Kruchinova, K. V. Skaletsky, E. K. Donets, A. M. Namitokov, M. V. Karibova, E. D. Kosmacheva
Publikováno v:
Российский кардиологический журнал, Vol 29, Iss 2S (2024)
Introduction. Constrictive pericarditis is a long-term consequence of any pathological process developing in the pericardium due to fibrinous thickening and calcification of its layers, which prevents normal cardiac diastolic filling. One of its form
Externí odkaz:
https://doaj.org/article/273fe0ee6d224de8b11994da3d6a7ec4
Autor:
Bilge Kurnaz Kaplan, Fatih Kaplan
Publikováno v:
Medicine Science, Vol 10, Iss 3, Pp 1047-8 (2021)
Brutons disease is an X-linked immunodeficiency. Recurrent bacterial infections are seen in patients with this disease. A 2-year-old male patient was brought to the otolaryngology clinic due to pain in both ears and tenderness. It was learned from hi
Externí odkaz:
https://doaj.org/article/1d738daf402b4ca68e47c251faf4ab42
Akademický článek
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Autor:
Fatih Kaplan, Bilge Kaplan
Publikováno v:
Medicine Science, Vol 10, Iss 3, Pp 1047-8 (2021)
Brutons disease is an X-linked immunodeficiency. Recurrent bacterial infections are seen in patients with this disease. A 2-year-old male patient was brought to the otolaryngology clinic due to pain in both ears and tenderness. It was learned from hi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::adad07cf8a04e47ac4d994a40a421845
https://doi.org/10.5455/medscience.2021.05.158
https://doi.org/10.5455/medscience.2021.05.158
Intoduction: Bruton’s disease occurs in approximately 1 in 200,000 newborns. In many cases, it leads to death because of the expensive treatment that is free only until 18 years old. Due to the rare occurrence therefore - the rate of disease detect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4486::0ff63f6e55525cff3dcc85b308dbefe6
https://hdl.handle.net/20.500.12415/3434
https://hdl.handle.net/20.500.12415/3434
Autor:
Walter H. Hitzig
Publikováno v:
European Journal of Pediatrics. 162:289-304
Fifty years ago a new disease, agammaglobulinaemia, was described. This was made possible by a great number of preceding technical innovations and theories on different fields of research, in particular haematology, microbiology/immunology and basic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5af0858a316170b6271ccfd4c521a5ca
https://doi.org/10.1007/s00431-003-1153-7
https://doi.org/10.1007/s00431-003-1153-7
Autor:
Uludağ Üniversitesi/Tıp Fakültesi/Çocuk Sağlığı ve Hastalıkları Anabilim Dalı/Çocuk İmmünoloji Bilim Dalı., Kılıç, Sara Şebnem
Antikor yapım defekti en sık görülen immün yetmezlik grubudur. Bu hastalık grubu tüm immünglobulinlerin düşük olduğu agammaglobulinemi gibi ağır hastalık tablolarını içerebildiği gibi daha hafif klinik seyirli normal immunglobulin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______9458::afc6425758fb94125bb17b6e034648f9
http://hdl.handle.net/11452/11650
http://hdl.handle.net/11452/11650
Akademický článek
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Autor:
Guadalupe García-Reyes, Rosa Maria Cortes-Grimaldo, Carlos Torres-Lozano, Efrain Montaño-Gonzalez, Cecy Garcia-Cobas, Ileana Madrigal, Margarita Ortega-Cisneros, Sergio Mendez-Santillan, Maria Enriqueta Nuñez-Nuñez
Publikováno v:
The World Allergy Organization Journal
Background To know the association between X-linked Agammaglobulinemia and Moebius Syndrome. The X-linked Agammaglobulinemia or Bruton disease, is characterized by the absence of B cells and decreased serum immunoglobulin. The defective gen codes a t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::147ff0cc628c9ca9b1c5a3f013987ebd
https://doi.org/10.1097/01.wox.0000411745.29602.67
https://doi.org/10.1097/01.wox.0000411745.29602.67
Akademický článek
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