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Inhibitor development upon switching from plasma-derived to recombinant factor VIII in previously untreated patients with severe hemophilia A: the PUP-SWITCH study.
Miri S, Rosendaal FR, Kavakli K, Eshghi P, Moghaddam SM, Scardo S, Habibpanah B, Elalfy M, Halimeh S, Nicolò G, Gökçebay D, Özbek N, Celkan T, Mohammadi A, Karimi M, Shahsavani A, Yılmaz B, Albayrak C, Gunes B, Kaya Z, Ay Y, Akbayram S, Sarper N, Mannucci PM, Peyvandi F; PUP-SWITCH Study Group. Miri S, et al. Among authors: sarper n. Res Pract Thromb Haemost. 2024 Oct 18;8(8):102595. doi: 10.1016/j.rpth.2024.102595. eCollection 2024 Nov. Res Pract Thromb Haemost. 2024. PMID: 39649130 Free PMC article.
Retrospective analysis of hemophilia B in Turkey: identifying main characteristics and treatment options.
Zülfikar B, Koç B, Şahin F, Şaşmaz Hİ, Kavaklı K, Balkan C, Antmen AB, Akbayram S, Güvenç B, Okan V, Türkkan E, Albayrak C, Albayrak D, Sarper N, Celkan TT, Ayyıldız O, Aksu S, Patıroğlu T, Şalcıoğlu Z, Güneş AM, Torun YA, Çalışkan Ü, Tokgöz H, Ay Y, Özdemir GN, Sönmez M, Ünal E, Öner AF, Güler N, Küpesiz OA, Ören H, Karaman S, Ünüvar A, Dağlı M, Demir AM, Söker M, Alioğlu B, Kaya Z, Ayhan AC, Bıçakçı Z, Aral YZ, Ar MC. Zülfikar B, et al. Among authors: sarper n. Res Pract Thromb Haemost. 2024 Oct 10;8(7):102588. doi: 10.1016/j.rpth.2024.102588. eCollection 2024 Oct. Res Pract Thromb Haemost. 2024. PMID: 39582809 Free PMC article.
Identification of the molecular etiology in rare congenital hemolytic anemias using next-generation sequencing with exome-based copy number variant analysis.
Isik E, Aydinok Y, Albayrak C, Durmus B, Karakas Z, Orhan MF, Sarper N, Aydın S, Unal S, Oymak Y, Karadas N, Turedi A, Albayrak D, Tayfun F, Tugcu D, Karaman S, Tobu M, Unal E, Ozcan A, Unal S, Aksu T, Unuvar A, Bilici M, Azik F, Ay Y, Gelen SA, Zengin E, Albudak E, Eker I, Karakaya T, Cogulu O, Ozkinay F, Atik T. Isik E, et al. Among authors: sarper n. Eur J Haematol. 2024 Jul;113(1):82-89. doi: 10.1111/ejh.14194. Epub 2024 Mar 31. Eur J Haematol. 2024. PMID: 38556258
Taurine deficiency as a driver of aging.
Singh P, Gollapalli K, Mangiola S, Schranner D, Yusuf MA, Chamoli M, Shi SL, Lopes Bastos B, Nair T, Riermeier A, Vayndorf EM, Wu JZ, Nilakhe A, Nguyen CQ, Muir M, Kiflezghi MG, Foulger A, Junker A, Devine J, Sharan K, Chinta SJ, Rajput S, Rane A, Baumert P, Schönfelder M, Iavarone F, di Lorenzo G, Kumari S, Gupta A, Sarkar R, Khyriem C, Chawla AS, Sharma A, Sarper N, Chattopadhyay N, Biswal BK, Settembre C, Nagarajan P, Targoff KL, Picard M, Gupta S, Velagapudi V, Papenfuss AT, Kaya A, Ferreira MG, Kennedy BK, Andersen JK, Lithgow GJ, Ali AM, Mukhopadhyay A, Palotie A, Kastenmüller G, Kaeberlein M, Wackerhage H, Pal B, Yadav VK. Singh P, et al. Among authors: sarper n. Science. 2023 Jun 9;380(6649):eabn9257. doi: 10.1126/science.abn9257. Epub 2023 Jun 9. Science. 2023. PMID: 37289866 Free PMC article.
81 results