Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Fatma Düşünür Günsen"'
Autor:
Ceyda Tunakan Dalgıç, Fatma Düşünür Günsen, Gökten Bulut, Emine Nihal Mete Gökmen, Aytül Zerrin Sin
Publikováno v:
Case Reports in Immunology, Vol 2018 (2018)
Hereditary angioedema due to C1-inhibitor deficiency (C1-INH-HAE) is a rare, autosomal dominant disorder. The management of pregnant patients with C1-INH-HAE is a challenge for the physician. Intravenous plasma-derived nanofiltered C1-INH (pdC1INH) i
Externí odkaz:
https://doaj.org/article/3724ffd722254163b9b72d21f42ccf96
Publikováno v:
Akademik Gastroenteroloji Dergisi. 17:41-43
Eozinofilik özofajit; özofagus mukozasında eozinofilik infiltrasyon ile karakterize kronik, immün aracılı bir tablodur. Erişkinlerde özofageal disfonksiyon semptomları olan disfaji, gıda takılma hissi, regürjitasyon, kusma ve göğüs ağ
Autor:
Fatma Düşünür Günsen, Aytül Sin
Publikováno v:
TOTBID Dergisi. 18
WOS: 000452210500009
We report the case of a 35-year-old woman allergic to detemir, neutral protamine Hagedorn, and glargine. Initially, local reactions to the insulin preparations occurred, which continued even after the types of insulin and th
We report the case of a 35-year-old woman allergic to detemir, neutral protamine Hagedorn, and glargine. Initially, local reactions to the insulin preparations occurred, which continued even after the types of insulin and th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f2dd63b488ef4fedbe0118fad8f70ef
https://hdl.handle.net/11454/31025
https://hdl.handle.net/11454/31025
Publikováno v:
Case Reports in Immunology
Case Reports in Immunology, Vol 2018 (2018)
Case Reports in Immunology, Vol 2018 (2018)
WOS: 000426177100001
PubMed ID: 29666724
Hereditary angioedema due to C1-inhibitor deficiency (C1-INH-HAE) is a rare, autosomal dominant disorder. The management of pregnant patients with C1-INH-HAE is a challenge for the physician. Intrave
PubMed ID: 29666724
Hereditary angioedema due to C1-inhibitor deficiency (C1-INH-HAE) is a rare, autosomal dominant disorder. The management of pregnant patients with C1-INH-HAE is a challenge for the physician. Intrave
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5753299e06a88c0df2aa593dacb13c5
https://hdl.handle.net/11454/31320
https://hdl.handle.net/11454/31320