Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Burçin Beken"'
Publikováno v:
Journal of Pediatric Emergency and Intensive Care Medicine, Vol 10, Iss 1, Pp 48-52 (2023)
Middle lobe syndrome is a well-defined clinical and radiological entity in the pediatric literature, The causes include many pathologies such as asthma, lymphadenopathy, tumor, foreign body aspiration, granulation tissue, mucus plug, bronchopulmonary
Externí odkaz:
https://doaj.org/article/845f4f17498f4707b66414aa846c056e
Publikováno v:
Namık Kemal Tıp Dergisi, Vol 9, Iss 3, Pp 249-254 (2021)
Aim:Atopic dermatitis (AD) is the most common chronic skin disease of childhood. Although eczema may be a prominent finding in some primary immune deficiencies, there are very few studies conducted on the frequency of hypogammaglobulinemia in patient
Externí odkaz:
https://doaj.org/article/93f5e65bc540473d8a28659579c6b588
Publikováno v:
Turkish Journal of Hematology, Vol 31, Iss 2, Pp 209-210 (2014)
Externí odkaz:
https://doaj.org/article/42da894c563d4d28ae7a8b97730fc96e
Publikováno v:
Turkish Journal of Hematology, Vol 31, Iss 2, Pp 199-200 (2014)
Externí odkaz:
https://doaj.org/article/88f467d8c4bb4344a10f40a8d68af5e9
Publikováno v:
World Journal of Pediatrics. 18:753-760
Personal genetic predisposition and early life environmental factors are important for the development of childhood asthma. We aimed to search whether egg, milk and mite sensitizations at 0-2 years old are risk factors for asthma symptoms at 9-11 yea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::476fc4c53e58d3a2c25279be90b39862
https://doi.org/10.1007/s12519-022-00579-5
https://doi.org/10.1007/s12519-022-00579-5
Publikováno v:
European Journal of Pediatrics. 181:2839-2847
The SARS-CoV-2 virus has infected more than 235 million people since it was accepted as a pandemic in March 2020. Although a milder disease is seen in the pediatric age group, the extent of lung damage and its long-term effects are still unknown. In
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca90be9647006fb865d02909ac0e7f55
https://doi.org/10.1007/s00431-022-04493-w
https://doi.org/10.1007/s00431-022-04493-w
Autor:
Burcin Beken, Selin Aytac, Gunay Balta, Baris Kuskonmaz, Duygu Uckan, Sule Unal, Mualla Cetin, Fatma Gumruk
Publikováno v:
Haematologica, Vol 103, Iss 2 (2018)
Familial hemophagocytic lymphohistiocytosis is an autosomal recessive, life-threatening condition characterized by defective immune response. A retrospective analysis was performed on 57 patients diagnosed with familial hemophagocytic lymphohistiocyt
Externí odkaz:
https://doaj.org/article/b5ff11a0fc9d4473a9225a7780271ba8