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Page 1
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: ay y. 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.
Restoring hippocampal glucose metabolism rescues cognition across Alzheimer's disease pathologies.
Minhas PS, Jones JR, Latif-Hernandez A, Sugiura Y, Durairaj AS, Wang Q, Mhatre SD, Uenaka T, Crapser J, Conley T, Ennerfelt H, Jung YJ, Liu L, Prasad P, Jenkins BC, Ay YA, Matrongolo M, Goodman R, Newmeyer T, Heard K, Kang A, Wilson EN, Yang T, Ullian EM, Serrano GE, Beach TG, Wernig M, Rabinowitz JD, Suematsu M, Longo FM, McReynolds MR, Gage FH, Andreasson KI. Minhas PS, et al. Among authors: ay ya. Science. 2024 Aug 23;385(6711):eabm6131. doi: 10.1126/science.abm6131. Epub 2024 Aug 23. Science. 2024. PMID: 39172838
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: ay y. Eur J Haematol. 2024 Jul;113(1):82-89. doi: 10.1111/ejh.14194. Epub 2024 Mar 31. Eur J Haematol. 2024. PMID: 38556258
Congenital fibrinogen disorders: a retrospective clinical and genetic analysis of the Prospective Rare Bleeding Disorders Database.
Mohsenian S, Palla R, Menegatti M, Cairo A, Lecchi A, Casini A, Neerman-Arbez M, Asselta R, Scardo S, Siboni SM, Blatny J, Zapletal O, Schved JF, Giansily-Blaizot M, Halimeh S, Daoud MA, Platokouki H, Pergantou H, Schutgens REG, Van Haaften-Spoor M, Brons P, Laros-van Gorkom B, Van Pinxten E, Borhany M, Fatima N, Mikovic D, Saracevic M, Özdemir GN, Ay Y, Makris M, Lockley C, Mumford A, Harvey A, Austin S, Shapiro A, Williamson A, McGuinn C, Goldberg I, De Moerloose P, Peyvandi F. Mohsenian S, et al. Among authors: ay y. Blood Adv. 2024 Mar 26;8(6):1392-1404. doi: 10.1182/bloodadvances.2023012186. Blood Adv. 2024. PMID: 38286442 Free PMC article.
Central nervous system thrombosis in pediatric acute lymphoblastic leukemia in Turkey: A multicenter study.
Guzelkucuk Z, Karapınar DY, Gelen SA, Tokgoz H, Ozcan A, Ay Y, Bahadır A, Ozbek NY, Oren AC, Ayhan AC, Akyay A, Akıncı B, Karadas N, Unuvar A, Oren H, Fettah A, Kaya Z, Isık B, Eker İ, Karaman S, Yıldırım AT, Orhan MF, Oymak Y, Timur C, Yazici N, Simsek A, Karakurt N, Toret E, Evim MS. Guzelkucuk Z, et al. Among authors: ay y. Pediatr Blood Cancer. 2023 Aug;70(8):e30425. doi: 10.1002/pbc.30425. Epub 2023 May 17. Pediatr Blood Cancer. 2023. PMID: 37194482
Tension Pneumothorax in Prehospital Setting.
Ay Y, Canakci ME. Ay Y, et al. Prehosp Disaster Med. 2021 Aug;36(4):498. doi: 10.1017/S1049023X21000479. Epub 2021 Jun 2. Prehosp Disaster Med. 2021. PMID: 34074351 No abstract available.
82 results