Journal of Hematology

ISSN 1927-1212 print
ISSN 1927-1220 online
Frequency: Quarterly
Journal Access: Open Access
Journal scope: Journal of Hematology is an international, peer-reviewed journal, publishing original contributions describing basic research and clinical investigation of hematology and transfusion medicine, on the cellular, molecular, prevention, diagnosis, therapy and prognosis aspects.
Indexed and covered by: Chemical Abstract (CA); Directory of Open Access Journals (DOAJ);
Worldcat; Google; Google Scholar; JournalTOCs; PubMed: selected citations.
Journal archiving and digital preservation: Portico


  • Associations Between Initial Presentation of Multiple Myeloma and Renal Function: the Experience of Two European Centers

    This study aimed to describe the baseline renal, histopathological and hematological characteristics and any clinical or biochemical associations of patients with a first coded diagnosis of multiple myeloma (MM).

  • Treatment of Anemia Owing to Increased Menstrual Blood Loss: Activity of Physiological Modulators

    Heavy menstrual bleeding can lead to iron-deficiency anemia. The objective was to ascertain whether daily administration of a formula containing iron, essential amino acids, ascorbic acid and B-group vitamins for 28 days will increase hemoglobin levels by 0.5 g/dL and reduce menstrual bleeding.

  • Concurrent Presentation of High-Grade Lymphoma and Metastatic Pancreatic Neuroendocrine Tumor 14 Years After Renal Transplant

    The development of malignancy, especially lymphoma, is common after solid organ transplant. However, concurrent malignancies are rare and result in a diagnostic and treatment dilemma, particularly in the post-transplant setting.

  • Arterial and Venous Estimation of Hemoglobin: A Correlational Study

    The objective of this study was to identify the correlation between arterial blood gas (ABG) hemoglobin and venous hemoglobin in acutely ill patients.

  • A Rare Variant of Aggressive T-Cell Large Granular Lymphocyte Leukemia Associated With Hepatic Fibrosis and Trisomy 8

    Aggressive T-cell large granular lymphocytic leukemia (T-LGL) is a rare entity with a poor prognosis, the main clinical findings being splenomegaly, lymphadenopathy, thrombocytopenia and a CD3+/CD56+ phenotype.

  • Mobile Thrombus in the Ascending Aorta Associated With Acute Myocardial Infarction

    The presence of thrombus in the ascending aorta is uncommon but it has been implicated in systemic thromboembolism.





Featured Article


Potential Benefits of Metformin Use in Sickle Cell Anemia
Sickle cell anemia (SCA) is one of the most important genetic disorders known to mankind. Even with the impressive advances in medical science, effective treatment and cure remain challenging. Currently available treatments including hydroxyurea, which is the only FDA approved drug for SCA, and hemopoietic stem cell transplantation all have significant limitations, so the search for new therapeutic options continues. Read the Full Text

Beta-Globin Haplotypes and Alpha-Thalassemia 3.7 kb Deletion in Sickle Cell Disease Patients From the Occidental Brazilian Amazon
Sickle cell disease (SCD) includes a group of inherited red blood cell disorders. SCD patients vary widely from person to person. We describe βS and βC haplotypes and α-thalassemia 3.7 kb genotypes from SCD patients Fundacao Hospitalar de Hematologia e Hemoterapia do Amazonas, Manaus, AM. Our survey included 139 HbSS and 11 HbSC patients. Molecular genotypes have been identified by PCR-RFLP and α-thalassemia 3.7 kb deletion by ASO-PCR. Male/female distribution was 42.3%/57.7%. Read the Full Text


Ebstein-Barr Virus-Negative Clonal Plasma Cell Proliferations Associated With Systemic Involvement of Primary Cutaneous T-Cell Lymphoma
We describe a 66-year-old man with a long-standing history of squamous cell carcinoma of the head and neck region who developed nodular-sclerosing subtype of classical Hodgkin lymphoma and primary cutaneous CD8-positive, cytotoxic variant of mycosis fungoides over a 1-year period of time. Within a few months of his diagnosis of primary cutaneous T-cell lymphoma, he developed systemic involvement of T-cell lymphoma in an axillary lymph node, bone marrow and lung. Full Text

Current Issue

Past Issues

Vol. 6, No. 1, Mar 2017

Table of Contents

Original Article

Experimental Research of Blood Collected From the Peripheral Side of the Fluid Infusion Site That Is Not Affected by Fluid Infusion Abstract HTML PDF
Shotaro Koike, Toshiaki Takeda 1-5
Reference Value Profile for Healthy Individuals From the Aljouf region of Saudi Arabia Abstract HTML PDF
Abozer Y. Elderdery, Abdulaziz S. Alshaiban 6-11
Warm Autoimmune Hemolytic Anemia: Clinical Profile and Management Abstract HTML PDF
Sreenivasa Rao Sudulagunta, Monica Kumbhat, Mahesh Babu Sodalagunta, Aravinda Settikere Nataraju, Shiva Kumar Bangalore Raja, Keshava Chandra Thejaswi, Raj Deepak, Asif Hussain Mohammed, Sony P. Sunny, Amulya Visweswar, Mikita Suvarna, Rashmi Nanjappa 12-20

Case Report

A Unique Neuropsychiatric Syndrome in Variant Hereditary Coproporphyria: Case Report and Review of the Literature Abstract HTML PDF
Alex Baumgartner, Peter J. Quesenberry 21-24
Transient Abnormal Myelopoiesis: A Varied Spectrum of Clinical Presentation Abstract HTML PDF
Amitabh Singh, Anirban Mandal, Vijay Guru, Sindhu Srinivasan, Rachna Seth 25-28
Multiple Myeloma-Induced Hyperammonemic Encephalopathy Abstract HTML PDF
Ghulam Murtaza, Hannah Lu, Anadil Faqah, Nicholas Konowitz, Aneesh Kuruvilla, Sujeen Adhikari 29-31
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Journal of Hematology, quarterly, ISSN 1927-1212 (print), 1927-1220 (online), published by Elmer Press Inc.            
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