E-ISSN: 1308-5263
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After papers have been accepted for publication, manuscript files are forwarded to the statistical and English language editors before publishing. Editors will make changes to the manuscript to ensure it adheres to TJH requirements. Significant changes or concerns are referred to corresponding authors for editing. 

Turk J Hematol: ()
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REVIEW
1.Late Effects of Therapy in Childhood Acute Lymphoblastic Leukemia Survivors
Hande Kızılocak, Fatih Okçu
doi: 10.4274/tjh.2018.0150  Page 

RESEARCH ARTICLE
2.A novel ATP6V0A2 mutation causing recessive cutis laxa with unusual manifestations of bleeding diathesis and defective wound healing
İlker Karacan, Reyhan Diz Küçükkaya, Fatma Nur Karakuş, Seyhun Solakoğlu, Aslıhan Tolun, Veysel Sabri Hançer, Eda Tahir Turanlı
doi: 10.4274/tjh.2018.0325  Page 

3.Different presentations of patients with transcobalamin II deficiency: A single center experience from Turkey
Selma Ünal, Feryal Karahan, Tuğba Arıkoğlu, Asuman Akar, Semanur Kuyucu
doi: 10.4274/tjh.2018.0230  Page 

4.Evaluation of Cardiac Parameters in Bone Marrow Transplant Patients: Effect of pulmonary artery pressure on survival
Ali Caner Özdöver, İlknur Gündeş, Melya Pelin Kırık, Handan Haydaroğlu Şahin, Murat Sucu, Mustafa Pehlivan
doi: 10.4274/tjh.2018.0015  Page 

5.Frequent Mutation in the FTL Gene Causing Hyperferritinemia Cataract Syndrome in Turkish Population is c.-160 A>G
Burhan Balta, Murat Erdoğan, Aslıhan Kiraz, Serdal Korkmaz, Alperen Ağadayı
doi: 10.4274/tjh.2018.0194  Page 

6.Long-term Dental Anomalies After Pediatric Cancer Treatment in Children
Gülser Kılınç, Gülçin Bulut, Fahinur Ertuğrul, Hale Ören, Bengü Demirağ, Ayşe Demiral, Serap Aksoylar, Emine Serra Kamer, Hülya Ellidokuz, Nur Olgun
doi: 10.4274/tjh.2018.0248  Page 

7.The Investigation of Relationship Between Fok1 and Col1A1 Gene Polymorphisms and Development of Treatment-Related Bone Complications in Children with Acute Lymphoblastic Leukemia
Melek Erdem, Özlem Tüfekçi, Sefa Kızıldağ, Şebnem Yılmaz, Deniz Kızmazoğlu, Berna Eroğlu Filibeli, Hale Ören
doi: 10.4274/tjh.2018.0221  Page 

8.Tumor Necrosis Factor Alpha (TNF-α) –308G/A Polymorphism and the Risk of Multiple Myeloma: A Meta-analysis of Pooled Data from 12 Case-control Studies
Yingchao Li, Yong Lin
doi: 10.4274/Tjh.2018.0238  Page 

IMAGES IN HEMATOLOGY
9.A case of SF3B1 positive myelodysplastic/myeloproliferative neoplasm with ring sideroblasts and thrombocytosis
Alejandro Lazo-langner, Bekim Sadikovic
doi: 10.4274/tjh.2018.0267  Page 

10.Rare Presentation of Herpes Virus Lesions in a Case with Acute Pre-B Lymphoblastic Leukemia
Eylem Kaymaz, Zeliha Güzelküçük, Melek Işık, Neşe Yaralı
doi: 10.4274/tjh.2018.0372  Page 

11.Auer Rod-Like Inclusions in B-cell prolymphocytic leukemia
Yantian Zhao, Juan Lv
doi: 10.4274/tjh.2018.0192  Page 

12.Peutz–Jeghers syndrome:  A very rare cause of iron deficiency anemia
Fatma Demir Yenigürbüz, Uğur Deveci, Ebru Tuncez
doi: 10.4274/tjh.2018.0164  Page 

13.Vacuolization in Myeloid and Erythroid Precursors in a child with Menkes Disease
Seçil Sayın, Şule Ünal, Mualla Çetin, Fatma Gümrük
doi: 10.4274/tjh.2018.0104  Page 

LETTER TO EDITOR
14.A Successful Coronary Artery Bypass Operation with Intermittent Factor VIII Administration in a Hemophilia A Patient who Applied with Acute Myocardial Infarction: a rare and difficult case
Ulaş Serkan Topaloğlu, Rıfat Özmen, Recep Civan Yüksel, Murat Çetin, Gülşah Akyol
doi: 10.4274/tjh.2018.0271  Page 

15.Bendamustine and Rituximab Treatment, Chronic Lymphocytic Leukemia, Direct Antiglobulin Test, and false negative
Won Sriwijitalai, Viroj Wiwanitkit
doi: 10.4274/tjh.2018.0397  Page 

16.Wilm’s tumor-1 (WT1) rs16754 polymorphism and clinical outcome in acute myeloid leukemia
Mani Ramzi, Mohamad Moghadam, Nader Cohan
doi: 10.4274/tjh.2018.0277  Page 

17.Wilm's tumor-1 (WT1) rs16754 polymorphism
Pathum Sookaromdee, Viroj Wiwanitkit
doi: 10.4274/tjh.2018.0407  Page 

18.A Case of Blastic Plasmacytoid Dendritic Cell Neoplasm With Unusual Presentation
S. Dhariwal, M. Gupta
doi: 10.4274/tjh.2018.0181  Page 

19.A Novel Mutation In A Child With Atypical Wiskott-Aldrich Syndrome Complicated by Cytomegalovirus Infection
Zühre Kaya, Cansu Muluk, Şule Hakoloğlu, Lale Ş. Tufan
doi: 10.4274/tjh.2018.0187  Page 

20.Aggressive Clinicopathological Course Of Myeloma With t(3;16)(q21;q22) Cytogenetic Abnormality
Süreyya Bozkurt, Müfide Okay, C. İbrahim Haznedaroğlu
doi: 10.4274/tjh.2018.0049  Page 

21.Atypical Radiologic Image Characterized by Cavitary Lun Lesions In a Case With Hodgkin Lymphoma
Mahmut Buyuksimsek, Semra Paydas, Derya Gumurdulu, Cem Mirili, Ali Ogul, Abdullah Evren Yetisir, Mert Tohumcuoglu
doi: 10.4274/tjh.2018.0115  Page 

22.Clonal evolution of acute myeloid leukemia with CEBPA double mutations after long-term remission: case report and a literature review
Ying Li, Long Su
doi: 10.4274/tjh.2018.0215  Page 

23.EBV-related Diffuse Large B-cell lymphoma in a Patient with Angioimmunoblastic T Cell Lymphoma: A Case Presentation
Cem Şimşek, Başak Bostankolu, Ece Özoğul, Arzu Sağlam Ayhan, Ayşegül Üner, Yahya Büyükaşık
doi: 10.4274/tjh.2018.0023  Page 

24.Investigation Of Mdm2 Oncogene Copy Number Alterations in Cases With Chronic Lymphocytic Leukemia
Şule Darbas, Çiğdem Aydın, Ozan Salim, Sibel Berker Karauzum
doi: 10.4274/tjh.2018.0270  Page 

25.Kasabach-Merritt Syndrome in an Adult: A Comment
Sevgi Gözdaşoğlu
doi: 10.4274/tjh.2018.0356  Page 

26.Light chain myeloma with highly atypical plasma cells and extensive Auer rod-like inclusions
Dietmar Enko, Gernot Kriegshäuser
doi: 10.4274/tjh.2018.0197  Page 

27.Pediatric Deep Venous Thrombosis and Pulmonary Embolism: Can It Be Antiphospholipid Syndrome?
Fatma Demir Yenigürbüz, Hale Ören
doi: 10.4274/tjh.2018.0214  Page 

28.Prospective Evaluation of the Non-Compliant Severe Hemophilia Patients
Mehmet Can Uğur, Kaan Kavaklı
doi: 10.4274/tjh.2018.0281  Page 

29.The Coexistence of Chronic Lymphocytic Leukemia and Multiple Myeloma
Ceren Hangül, Orhan Kemal Yücel, Bahar Akkaya, Levent Undar, Sibel Berker Karaüzüm
doi: 10.4274/tjh.2018.0096  Page 

30.The impact of DNMT3A/FLT3-ITD/NPM1 on patients with acute myeloid leukemia after allogeneic hematopoietic stem cell transplantation
Long Su
doi: 10.4274/tjh.2018.0274  Page 

31.Bleomycin-induced flagellate dermatitis
Esra Turan Erkek, Ceren Nur Karaali, Güven Yılmaz, Emine Gültürk
doi: 10.4274/Tjh.2018.0317  Page 

32.Remarks on Myeloid Sarcoma in Children

doi: 10.4274/tjh.2019.0002  Page 

33.Venous thromboembolism in a young girl with duplication of inferior vena cava and protein S deficiency
Wei-li Liao, Ming-yang Shih, Jiaan-der Wang
doi: 10.4274/tjh.2018.0332  Page 

BRIEF REPORT
34.Assessment of Health-Related Quality of Life in Pediatric Acute Lymphoblastic Leukemia Survivors: Perceptions of Children, Siblings, and Parent
Deniz Kızmazoğlu, Seher Sarı, Melike Evim Sezgin, Arzu Kantarcıoğlu, Özlem Tüfekçi, Fatma Demir Yenigürbüz, Birol Baytan, Şebnem Yılmaz, Adalet Meral Güneş, Hale Ören
doi: 10.4274/tjh.2018.0351  Page 

35.Thalidomide for the Management of Bleeding Episodes in Patients with Hereditary Hemorrhagic Telangiectasia, Effects on Epistaxis Severity Score and Quality of Life
Mehmet Baysal, Elif G Ümit, Hakkı Onur Kırkızlar, Ali Caner Özdöver, Ahmet Muzaffer Demir
doi: 10.4274/tjh.2018.0190  Page 

 



Impact Factor (2017) = 0.650