Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Ahmet Mert Yanik"'
Autor:
Fatma Arikan, Pinar Ata, Senol Demir, Ozlem Yildirim, Özgür Mehtap, Atakan Erol, Bedrettin Orhan, Fahir Ozkalemkas, Meral Ulukoylu Menguc, Derya Demirtas, Ahmet Mert Yanik, Ozlem Candan, Tayfur Toptas, Ayse Tulin Tuglular
Publikováno v:
HemaSphere, Vol 7, p e87663b9 (2023)
Externí odkaz:
https://doaj.org/article/8375a465ec544096b6d06ddad0ef2dbf
Publikováno v:
Cureus.
Hereditary hyperferritinemia-cataract syndrome (HHCS) is a rare genetic condition characterized by persistent hyperferritinemia (usually ferritin >1,000 ng/mL) without tissue iron overload, with or without early-onset slow-progressing bilateral nucle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3aee407a41ac4abaa6c92e06fbca09e7
https://doi.org/10.7759/cureus.36253
https://doi.org/10.7759/cureus.36253
Autor:
Duygu Gül, Burçak Kayhan, Ahmet Mert Yanik, Erol Bat, Onur Tangur, İlhan Asude Akça, Adem Akbal, Özlem Baykal, Nurhayat Ozkan Sevencan, Ayse Rana Sarikaya, Yusif Jafarov
Publikováno v:
Volume: 3, Issue: 3 259-261
Medical Records
Medical Records
Although malignant melanoma is a rare type of skin cancer, it accounts for most skin cancer-related deaths. Foot lesions may be ignored by both patients and clinicians and could therefore lead to advanced disease. An acral melanoma may also be confus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9a8c83bdc3e4a320b9b42d2b757a928
https://dergipark.org.tr/tr/pub/medr/issue/64607/911263
https://dergipark.org.tr/tr/pub/medr/issue/64607/911263
