Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Fahri, Sahin"'
Publikováno v:
Turkish Journal of Hematology, Vol 40, Iss 3, Pp 197-201 (2023)
This survey study aimed to evaluate the level of awareness and knowledge of acquired hemophilia A (AHA) among physicians from various specialties. Data were collected by administering a questionnaire containing questions about two patient profiles to
Externí odkaz:
https://doaj.org/article/79ba391e605943bb878b3a9e19008a9f
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 45, Iss , Pp S35-S36 (2023)
Objective: Factor X deficiency (FXd) is a rare coagulation disorder that can be either hereditary or acquired. Case report: We characterized patients with FXd and evaluated their bleeding patterns and treatment strategies. Methodology: This retrospec
Externí odkaz:
https://doaj.org/article/4c866e69714a4f51a189882c56245b96
Publikováno v:
HemaSphere, Vol 7, p e184481b (2023)
Externí odkaz:
https://doaj.org/article/14b5629a3a18408885bff5b87ed3499d
Publikováno v:
HemaSphere, Vol 7, p e38881ba (2023)
Externí odkaz:
https://doaj.org/article/76a0e1fc694946489d2b03ec169dd9c4
Akademický článek
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Akademický článek
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Publikováno v:
European Medical Journal Hematology (2020)
Externí odkaz:
https://doaj.org/article/15d1024681414d67a5c5b30d276fe6cc
Autor:
Muhammed Eyyub Polat, Elif Sarı, Lokman Hekim Tanriverdi, Mehmet Gunata, Murat Aladag, Abdullah Fahri Sahin, Burhan Ates, Hakan Parlakpinar
Methotrexate (MTX) is an important drug for rheumatic and non-rheumatic disease therapy. MTX has been associated with many adverse effects ranging from asymptomatic transaminase elevation to fibrotic tissue formation and fatal hepatic necrosis due to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ebdf1b00da346d26de50e223bd425cd5
https://doi.org/10.22541/au.168490817.77526721/v1
https://doi.org/10.22541/au.168490817.77526721/v1
Autor:
Fusun Gediz, Bahriye Kadriye Payzin, Ozlem Zekiye Cakmak, Yusuf Uzum, Damla Ernur, Fahri Sahin
Publikováno v:
Hematology Reports, Vol 9, Iss 1 (2017)
Paroxysmal nocturnal hemoglobinuria (PNH) is a disease which diagnosis may be delayed due to variable clinical findings. We describe herein a case of PNH in a 21 year old woman who admitted with complaints of chronic weakness, intermittent spontaneou
Externí odkaz:
https://doaj.org/article/fdc3747d27564153ad2e0f61b3e3dd22
Autor:
Asu Fergun Yilmaz, Nur Soyer, Nazan Ozsan, Seckin Cagirgan, Ajda Gunes, Melda Comert, Fahri Sahin, Guray Saydam, Nur Selvi Gunel, Filiz Vural
Publikováno v:
Case Reports in Hematology, Vol 2017 (2017)
Myeloid or granulocytic sarcoma (GS) is a tumoral lesion consisting of immature granulocytic cells. It is a rare entity during the course of CML patients especially after allogeneic stem cell transplantation (SCT). Relapse without bone marrow involve
Externí odkaz:
https://doaj.org/article/61365041674e4dd38fa3fcfd57014074