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收藏分享 收藏 Genetic and clinical characterization of factor VII deficiency: insights from 34 Turkish patients因子Ⅶ缺乏症的遗传与临床特征：来自34例土耳其患者的见解
Atik, Tahir; Durmus Ozen, Basak; Isik, Esra; Avci Durmusalioglu, Enise; Sarper, Nazan; Albayrak, Canan; Kupesiz, Alphan; Sezgin Evim, Melike; Azizoglu, Mehmet; Albayrak, Davut; Kupesiz, Funda Tayfun; Tuysuz Kintrup, Gulen; Unal, Ekrem; Ozcan, Alper; Kavakli, Kaan; Ozkinay, Ferda 分享 收藏 Risk factors for neurologic sequelae in children and adolescents with hemophilia after intracranial hemorrhage儿童青少年血友病颅内出血后神经系统后遗症的危险因素分析Evim, Melike Sezgin; Unuvar, Aysegul; Albayrak, Canan; Zengin, Emine; Yilmaz, Ebru; Kaya, Zuhre; Karadas, Nihal; Ertekin, Mehtap; Uzel, Hulya; Ozdemir, Gul Nihal; Albayrak, Davut; Kupesiz, Funda Tayfun; Bahadir, Aysenur; Tokgoz, Huseyin; Karaman, Kamuran; Yilmaz, Baris; Akbayram, Sinan; Gunes, Burcak Tatli; Apak, Burcu Belen; Acipayam, Can; Aral, Yusuf Ziya; Karaman, Serap; Oren, Hale 分享 收藏 Retrospective analysis of hemophilia B in Turkey: identifying main characteristics and treatment optionsZulfikar, Bulent; Koc, Basak; Sahin, Fahri; Sasmaz, Hatice Ilgen; Kavakli, Kaan; Balkan, Can; Antmen, Ali Buelent; Akbayram, Sinan; Guvenc, Birol; Okan, Vahap; Turkkan, Emine; Albayrak, Canan; Albayrak, Davut; Sarper, Nazan; Celkan, Tuelin Tiraje; Ayyildiz, Orhan; Aksu, Salih; Patiroglu, Tuerkan; Salcioglu, Zafer; Gunes, Adalet Meral; Torun, Yasemin Altuner; Caliskan, Umran; Tokgoz, Huseyin; Ay, Yilmaz; Ozdemir, Gul Nihal; Sonmez, Mehmet; Unal, Ekrem; Oner, Ahmet Fayik; Guler, Nil; Kupesiz, Osman Alphan; Oren, Hale; Karaman, Serap; Unuvar, Ayegul; Dagli, Mehmet; Demir, Ahmet Muzaffer; Soker, Murat; Alioglu, Buelent; Kaya, Zuehre; Ayhan, Aylin Canbolat; Bicakci, Zafer; Aral, Yusuf Ziya; Ar, Muhlis Cem 分享 收藏 Different Kinetics and Risk Factors for Isolated Extramedullary Relapse after Allogeneic Hematopoietic Stem Cell Transplantation in Children with Acute Leukemia儿童急性白血病异基因造血干细胞移植后孤立性髓外复发的不同动力学及危险因素Hazar, Volkan; Ozturk, Gulyuz; Yalcin, Koray; Uygun, Vedat; Aksoylar, Serap; Kupesiz, A.; Bozkaya, Ikbal Ok; Karagun, Barbaros Sahin; Bozkurt, Ceyhun; Ileri, Talia; Atay, Didem; Kocak, Ulker; Karasu, Gulsun Tezcan; Yesilipek, Akif; Gokce, Muge; Kansoy, Savas; Kintrup, Gulen Tuysuz; Karakukcu, Musa; Okur, Fatma Visal; Ertem, Mehmet; Kaya, Zuhre; Gursel, Orhan; Yaman, Yontem; Ozbek, Namik; Antmen, Bulent; Tufekci, Ozlem; Albayrak, Canan; Aksoy, Basak Adakli; Sezgin, Gulay; Albayrak, Davut; Evim, Melike Sezgin; Zengin, Emine; Pekpak, Esra 分享 收藏 Marked overlap of four genetic syndromes with dyskeratosis congenita confounds clinical diagnosisWalne, Amanda J.; Collopy, Laura; Cardoso, Shirleny; Ellison, Alicia; Plagnol, Vincent; Albayrak, Canan; Albayrak, Davut; Kilic, Sara Sebnem; Patiroglu, Turkan; Akar, Haluk; Godfrey, Keith; Carter, Tina; Marafie, Makia; Vora, Ajay; Sundin, Mikael; Vulliamy, Thomas; Tummala, Hemanth; Dokal, Inderjeet 分享 收藏 Bleeding and non-bleeding phenotypes in patients with GGCX gene mutationsWatzka, Matthias; Geisen, Christof; Scheer, Monika; Wieland, Regina; Wiegering, Verena; Doerner, Thomas; Laws, Hans-Juergen; Guemruek, Fatma; Hanalioglu, Sahin; Uenal, Sule; Albayrak, Davut; Oldenburg, Johannes 分享 收藏 SNX10 Mutations Define a Subgroup of Human Autosomal Recessive Osteopetrosis With Variable Clinical SeveritySNX10突变定义了具有可变临床严重程度的人类常染色体隐性骨硬化症亚组Pangrazio, Alessandra; Fasth, Anders; Sbardellati, Andrea; Orchard, Paul J.; Kasow, Kimberly A.; Raza, Jamal; Albayrak, Canan; Albayrak, Davut; Vanakker, Olivier M.; De Moerloose, Barbara; Vellodi, Ashok; Notarangelo, Luigi D.; Schlack, Claire; Strauss, Gabriele; Kuehl, Joern-Sven; Caldana, Elena; Lo Iacono, Nadia; Susani, Lucia; Kornak, Uwe; Schulz, Ansgar; Vezzoni, Paolo; Villa, Anna; Sobacchi, Cristina 分享 收藏 分享 收藏 分享 收藏 分享 收藏 分享 收藏 
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