日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Genetic heterogeneity in childhood leukemia/lymphoma: a Turkish cohort with strong predisposition

儿童白血病/淋巴瘤的遗传异质性:一项具有强烈易感性的土耳其队列研究

Onder, Gizem; Ozdemir, Ozkan; Taylan, Fulya; Canpolat, Cengiz; Yalcin, Koray; Erbey, Fatih; Sozmen, Banu Oflaz; Asarcikli, Fikret; Bayhan, Turan; Akcabelen, Yunus Murat; Yarali, Nese; Ozbek, Namik Yasar; Bozkaya, Ikbal Ok; Kacar, Dilek; Ergun, Berk; Akkus, Alper; Albayrak, Davut; Ince, Elif; Demirsoy, Ugur; Ozdemir, Gul Nihal; Dogru, Omer; Aras, Seda; Aydin, Eylul; Unal, Busra; Amanvermez, Ufuk; Dogan, Ozlem Akgun; Akyoney, Sezer; Sayitoglu, Muge; Nordgren, Ann; Bugra Agaoglu, Nihat; Ozbek, Ugur; Ng, Ozden Hatirnaz

A Multicenter Retrospective Study Comparing Immunosuppressive Therapy Combined with Eltrombopag to Immunosuppressive Therapy Alone as Frontline Treatment for Pediatric Severe Aplastic Anemia

一项多中心回顾性研究比较了免疫抑制疗法联合艾曲波帕与单独使用免疫抑制疗法作为儿童重型再生障碍性贫血一线治疗方案的疗效。

Atay, Didem; Yılmaz Karapınar, Deniz; Kaçar, Gonca; Karadaş, Nihal; Apak, Hilmi; Çakmaklı, Hasan Fatih; Gadashova, Aysha; Aksu, Tekin; Celkan, Tiraje; Yaralı, Neşe; Orhan, Mehmet Fatih; Özcan, Alper; Ertem, Mehmet; Aytaç, Selin; Ören, Hale; Akbayram, Sinan; Işık, Melek; Yılmaz, Şebnem; İleri, Talia; Büyükavcı, Mustafa; Karakükcü, Musa; Karapınar, Tuba Hilkay; Erbey, Fatih; Eker, İbrahim; Albayrak, Davut; Ünal, Şule

Retrospective analysis of hemophilia B in Turkey: identifying main characteristics and treatment options

土耳其B型血友病回顾性分析:主要特征及治疗方案的确定

Zülfikar, Bülent; Koç, Başak; Şahin, Fahri; Şaşmaz, Hatice İlgen; Kavaklı, Kaan; Balkan, Can; Antmen, Ali Bülent; Akbayram, Sinan; Güvenç, Birol; Okan, Vahap; Türkkan, Emine; Albayrak, Canan; Albayrak, Davut; Sarper, Nazan; Celkan, Tülin Tiraje; Ayyıldız, Orhan; Aksu, Salih; Patıroğlu, Türkan; Şalcıoğlu, Zafer; Güneş, Adalet Meral; Torun, Yasemin Altuner; Çalışkan, Ümran; Tokgöz, Hüseyin; Ay, Yılmaz; Özdemir, Gül Nihal; Sönmez, Mehmet; Ünal, Ekrem; Öner, Ahmet Fayik; Güler, Nil; Küpesiz, Osman Alphan; Ören, Hale; Karaman, Serap; Ünüvar, Ayşegül; Dağlı, Mehmet; Demir, Ahmet Muzaffer; Söker, Murat; Alioğlu, Bülent; Kaya, Zühre; Ayhan, Aylin Canbolat; Bıçakçı, Zafer; Aral, Yusuf Ziya; Ar, Muhlis Cem

Risk factors for neurologic sequelae in children and adolescents with hemophilia after intracranial hemorrhage

血友病患儿及青少年颅内出血后神经系统后遗症的危险因素

Evim, Melike Sezgin; Ünüvar, Ayşegül; Albayrak, Canan; Zengin, Emine; Yılmaz, Ebru; Kaya, Zühre; Karadaş, Nihal; Ertekin, Mehtap; Üzel, Hülya; Özdemir, Gül Nihal; Albayrak, Davut; Küpesiz, Funda Tayfun; Bahadır, Ayşenur; Tokgöz, Hüseyin; Karaman, Kamuran; Yılmaz, Barış; Akbayram, Sinan; Güneş, Burçak Tatlı; Apak, Burcu Belen; Acıpayam, Can; Aral, Yusuf Ziya; Karaman, Serap; Ören, Hale

Corrigendum to "Expanding the clinical and immunological phenotypes of PAX1-deficient SCID and CID patients" [Clinical Immunology 255 (2023) 109757]

对“扩展 PAX1 缺陷型 SCID 和 CID 患者的临床和免疫表型”的更正 [临床免疫学 255 (2023) 109757]

Yakici, Nalan; Kreins, Alexandra Y; Catak, Mehmet Cihangir; Babayeva, Royala; Erman, Baran; Kenney, Heather; Eke-Gungor, Hatice; Cea, Pablo A; Kawai, Tomoki; Bosticardo, Marita; Delmonte, Ottavia Maria; Adams, Stuart; Fan, Yu-Tong; Pala, Francesca; Turkyilmaz, Ayberk; Howley, Evey; Worth, Austen; Kot, Hakan; Sefer, Asena Pinar; Kara, Altan; Bulutoglu, Alper; Bilgic-Eltan, Sevgi; Yorgun Altunbas, Melek; Bayram Catak, Feyza; Karakus, Ibrahim Serhat; Karatay, Emrah; Tekeoglu, Sidem Didar; Eser, Metin; Albayrak, Davut; Citli, Senol; Kiykim, Ayca; Karakoc-Aydiner, Elif; Ozen, Ahmet; Ghosh, Sujal; Gohlke, Holger; Orhan, Fazil; Notarangelo, Luigi D; Davies, E Graham; Baris, Safa

Spontaneus Triplet Birth After Acute Lymphoblastic Leukemia Treatment

急性淋巴细胞白血病治疗后自然分娩三胞胎

Albayrak, Canan; Albayrak, Davut

Juvenile Myelomonocytic Leukemia in Turkey: A Retrospective Analysis of Sixty-five Patients

土耳其幼年型骨髓单核细胞白血病:65例患者的回顾性分析

Tüfekçi, Özlem; Koçak, Ülker; Kaya, Zühre; Yenicesu, İdil; Albayrak, Canan; Albayrak, Davut; Yılmaz Bengoa, Şebnem; Patıroğlu, Türkan; Karakükçü, Musa; Ünal, Ekrem; Ünal İnce, Elif; İleri, Talia; Ertem, Mehmet; Celkan, Tiraje; Özdemir, Gül Nihal; Sarper, Nazan; Kaçar, Dilek; Yaralı, Neşe; Özbek, Namık Yaşar; Küpesiz, Alphan; Karapınar, Tuba; Vergin, Canan; Çalışkan, Ümran; Tokgöz, Hüseyin; Sezgin Evim, Melike; Baytan, Birol; Güneş, Adalet Meral; Yılmaz Karapınar, Deniz; Karaman, Serap; Uygun, Vedat; Karasu, Gülsun; Yeşilipek, Mehmet Akif; Koç, Ahmet; Erduran, Erol; Atabay, Berna; Öniz, Haldun; Ören, Hale

Marked overlap of four genetic syndromes with dyskeratosis congenita confounds clinical diagnosis.

四种遗传综合征与先天性角化不良症有明显的重叠,这给临床诊断带来了困难

Walne Amanda J, Collopy Laura, Cardoso Shirleny, Ellison Alicia, Plagnol Vincent, Albayrak Canan, Albayrak Davut, Kilic Sara Sebnem, Patıroglu Turkan, Akar Haluk, Godfrey Keith, Carter Tina, Marafie Makia, Vora Ajay, Sundin Mikael, Vulliamy Thomas, Tummala Hemanth, Dokal Inderjeet