ISSN: 1300-7777 E-ISSN: 1308-5263
Turk J Hematol: 28 (4)
Volume: 28  Issue: 4 - 2011
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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 (1929 accesses)

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 (2256 accesses)

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 (1276 accesses)
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 (1702 accesses)

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 (3038 accesses)

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 (2121 accesses)

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 (1450 accesses)

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 (1733 accesses)

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 (1853 accesses)

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 (1488 accesses)

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 (2687 accesses)

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 (1877 accesses)

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 (1697 accesses)

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 (1421 accesses)
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 (1345 accesses)
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 (1510 accesses)
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 (1212 accesses)
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 (1367 accesses)
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 (1443 accesses)
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 (1536 accesses)
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 (1413 accesses)
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 (1235 accesses)
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 (1448 accesses)
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 (1387 accesses)
Abstract | Full Text PDF

 



Impact Factor (2016) = 0.686