Volume: 28  Issue: 4 - 2011
Show Abstracts | << Back
REVIEW
1.	The importance of studying inherited hematological disorders in ancient Anatolian populations Yeşim Doğan Alakoç, Nejat Akar doi: 10.5152/tjh.2011.43  Pages 257 - 263 Abstract | Full Text PDF
RESEARCH ARTICLE
2.	Beta-globin gene mutations in children with beta-thalassemia major from Şanlıurfa province, Turkey Ali Ayçiçek, Ahmet Koç, Zeynep Canan Özdemir, Hasan Bilinç, Abdurrahim Koçyiğit, Fuat Dilmeç doi: 10.5152/tjh.2011.86  Pages 264 - 268 Abstract | Full Text PDF
COMMENTARY
3.	Tracing the footsteps of IVS-I-130 G-C mutation of the human hemoglobin beta globin gene: From Şanlıurfa to Askeriye, Burdur, Turkey Çiğdem Altay doi: 10.5152/tjh.2011.99  Pages 269 - 270 Abstract | Full Text PDF
RESEARCH ARTICLE
4.	Antifungal prophylaxis in stem cell transplantation centers in Turkey Hamdi Akan doi: 10.5152/tjh.2011.81  Pages 271 - 275 Abstract | Full Text PDF
5.	The effects of Ankaferd® Blood Stopper on transcription factors in HUVEC and the erythrocyte protein profile Erkan Yılmaz, Şükrü Güleç, Didem Torun, İbrahim Celalettin Haznedaroğlu, Nejat Akar doi: 10.5152/tjh.2011.39  Pages 276 - 285 Abstract | Full Text PDF
6.	Long-term outcome in children with nutritional vitamin B12 deficiency Melike Sezgin Evim, Şahin Erdöl, Özlem Özdemir, Birol Baytan, Adalet Meral Güneş doi: 10.5152/tjh.2011.82  Pages 286 - 293 Abstract | Full Text PDF
7.	Clinical investigation of oral findings in inherited disorders of platelet function Müjgan Güngör Hatipoglu, Özden Kansu, Yahya Büyükaşık doi: 10.5152/tjh.2011.83  Pages 294 - 298 Abstract | Full Text PDF
8.	Factor V G1691A (Leiden) is a major etiological factor in Egyptian Budd-Chiari syndrome patients Tawhida Y. Abdel Ghaffar, Solaf M. Elsayed, Mohamed A. Sakr, Ezzat S. Elsobky, Sara M. Abdelhakam, Said Yousuf, Yonca Eğin, Nejat Akar doi: 10.5152/tjh.2011.84  Pages 299 - 305 Abstract | Full Text PDF
9.	Factor V G1691A (Leiden) and prothrombiG20210A gene mutation status, and thrombosis in patients with chronic myeloproliferative disorders Nur Soyer, Ali Şahin Küçükarslan, Fahri Şahin, Demet Çekdemir, Buket Kosova, Zuhal Eroğlu, Mahmut Töbü, Murat Tombuloğlu, Seçkin Çağırgan, Ayhan Dönmez, Filiz Vural, Güray Saydam doi: 10.5152/tjh.2011.85  Pages 306 - 311 Abstract | Full Text PDF
CASE REPORT
10.	Plasmacytoid dendritic cell tumor: A case report Füruzan Kacar Döger, Emel Dikicioğlu Çetin, Mine Hekimgil, Meltem Özdoğan Uslu, Gürhan Kadıköylü, Nazan Özsan, Ekin Şavk, Zahit Bolaman doi: 10.5152/tjh.2011.87  Pages 312 - 316 Abstract | Full Text PDF
11.	Involuntary movement in infants during vitamin B12 treatment Ayşe Tosun, Yusuf Ziya Aral, Emre Çeçen, Ayvaz Aydoğdu, Bilin Çetinkaya Çakmak doi: 10.5152/tjh.2011.18  Pages 317 - 322 Abstract | Full Text PDF
12.	Two rare hemoglobin variants in the Çukurova Region of Turkey: Hb E-Saskatoon and Hb G-Coushatta Ahmet Genç, Mehmet Akif Çürük doi: 10.5152/tjh.2011.88  Pages 323 - 326 Abstract | Full Text PDF
13.	Malignant lymphoma associated with Behçet’s disease: A report of 2 cases Ahmet Deniz Meydan, Bilge Gürsel, Nilgün Özbek, Bilge Can, Bedri Kandemir doi: 10.5152/tjh.2011.90  Pages 327 - 334 Abstract | Full Text PDF
LETTER TO EDITOR
14.	A survey of hematologists on compulsory health service in Turkey Zeynep Arzu Yegin, Mutlu Arat doi: 10.5152/tjh.2011.91  Pages 335 - 336 Abstract | Full Text PDF
15.	Unusual presentation of adrenal lymphoma observed with PET-CT Zeynep Gözde Özkan, Cüneyt Türkmen, Yasemin Şanlı, Mustafa Nuri Yenerel, Işık Adalet doi: 10.5152/tjh.2011.92  Pages 337 - 338 Abstract | Full Text PDF
16.	Scrotal abscess extending into the inguinal canal: A rare complication of multipl myeloma Fuat Özkan, Bülent Altınoluk, Sefa Resim, Mustafa Eren, Nazım Kankılıç doi: 10.5152/tjh.2011.93  Pages 339 - 340 Abstract | Full Text PDF
17.	Double heterozygosity of the thalassemic mutations term. Cd +6 C→G and IVS-I-110 in a Greek woman: A case presentation Stamatia Theodoridou, Vasilios Perifanis, Stella Kotsiopoulou, Olga Karakasidou, Vasiliki Aletra, Michael Alemayehou doi: 10.5152/tjh.2011.94  Pages 341 - 342 Abstract | Full Text PDF
18.	First report from Turkey of a rare frameshift mutation [codons 9/10 (+T)] in the beta-globin gene Ramazan Güneşaçar, M. Murat Çelik doi: 10.5152/tjh.2011.95  Pages 343 - 345 Abstract | Full Text PDF
19.	First observation of hemoglobin Crete [Beta129(H7) Ala>Pro] in the Turkish population Çiğdem Arslan, Selda Kahraman, Hayri Özsan, Nejat Akar doi: 10.5152/tjh.2011.48  Pages 346 - 347 Abstract | Full Text PDF
20.	The frequency of Factor V G1691A (Leiden) mutation in Iraqi Turks Arjan Esmael, Yonca Eğin, Nejat Akar doi: 10.5152/tjh.2011.46  Pages 348 - 349 Abstract | Full Text PDF
21.	Acute thrombotic complication of essential thrombocythemia Selami Koçak Toprak, Sema Karakuş, Feride İffet Şahin doi: 10.5152/tjh.2011.70  Pages 350 - 351 Abstract | Full Text PDF
22.	The frequency of factor V G1691A (Leiden) mutation in the healthy Kazakh population Hakkı Taştan doi: 10.5152/tjh.2011.96  Pages 352 - 353 Abstract | Full Text PDF
23.	A novel 110-bp insertion in a patient with homocysteinuria Didem Torun, Talia İleri, Kaan Gündüz, Nejat Akar doi: 10.5152/tjh.2011.44  Pages 354 - 356 Abstract | Full Text PDF
IMAGES IN HEMATOLOGY
24.	Overwhelming bone marrow Leishmaniasis Raihan Sajid, Adnan Qureshi doi: 10.5152/tjh.2011.97  Pages 357 - 358 Abstract | Full Text PDF

 

In authors and institutes In titles and abstracts In keywords In all