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  1. Patients receiving anticoagulant drugs must be carefully screened for drug-related problems, as such medications, including warfarin have narrow therapeutic ranges and a high potential for complications. Thus,...

    Authors: Fekede Bekele Daba, Fisihatsion Tadesse and Ephrem Engidawork
    Citation: BMC Hematology 2016 16:2
  2. High levels of fetal haemoglobin (HbF) decrease sickle cell anaemia (SCA) severity and leads to improved survival. According to in vivo and in vitro studies, butyrate increases HbF production. Its utilization ...

    Authors: Lamis Kaddam, Imad FdleAlmula, Omer Ali Eisawi, Haydar Awad Abdelrazig, Mustafa Elnimeiri, Florian Lang and Amal M. Saeed
    Citation: BMC Hematology 2015 15:19
  3. An individual with visceral Leishmaniasis (VL) commonly present with anemia and one of the VL treatment center in northwest Ethiopia has been recommended iron-folic acid supplementation to these patients. But ...

    Authors: Tadele Mulaw, Amare Tariku, Adino Tesfahun Tsegaye and Zegeye Abebe
    Citation: BMC Hematology 2018 18:29
  4. Infection is a major complication in aplastic anemia (AA) patients. Primary objectives of this study were to determine the prevalence of infections and to determine types of pathogens associated with infection...

    Authors: Rapee Lertpongpiroon, Ekarat Rattarittamrong, Thanawat Rattanathammethee, Chatree Chai-Adisaksopha, Adisak Tantiworawit, Parichat Salee and Lalita Norasetthada
    Citation: BMC Hematology 2018 18:35
  5. In pregnancy, hematological changes occur in order to meet the demands of the developing fetus and placenta, with major alterations in blood volume. Abnormal hematological profile affects pregnancy and its out...

    Authors: Angesom Gebreweld, Delayehu Bekele and Aster Tsegaye
    Citation: BMC Hematology 2018 18:15
  6. The serum ferritin assay is recommended in Sickle Cell Anemia (SCA) patients receiving regular transfusions. According to several authors, elevated iron stores indicating iron chelation corresponds to hyperfer...

    Authors: Jean-Robert Makulo, Karen Efombola Itokua, Rosette Kevani Lepira, Gloire Mavinga Bundutidi, Michel Ntetani Aloni, René Makuala Ngiyulu, Jean Lambert Gini and François Bompeka Lepira
    Citation: BMC Hematology 2019 19:3
  7. Langerhans cells (LC) are bone marrow-derived cells in the skin. The LC donor/recipient chimerism is assumed to influence the incidence and severity of graft-versus-host disease (GVHD) after hematopoietic stem...

    Authors: Sabrina Peters, Christian Junghanss, Anne Knueppel, Hugo Murua Escobar, Catrin Roolf, Gudrun Knuebel, Anett Sekora, Iris Lindner, Ludwig Jonas, Mathias Freund and Sandra Lange
    Citation: BMC Hematology 2016 16:11
  8. Hypertension is a major health problem worldwide. It can lead to cardiovascular disease and also leads to functional disturbances including hematological parameters. The abnormalities of haematological paramet...

    Authors: Bamlaku Enawgaw, Nigist Adane, Betelihem Terefe, Fikir Asrie and Mulugeta Melku
    Citation: BMC Hematology 2017 17:21
  9. Hemophilia A (HA) is an X-linked inherited bleeding disorder, resulting from a qualitative or quantitative deficiency of clotting factor VIII (FVIII). Antibodies against FVIII, also called inhibitors, block th...

    Authors: Amanda CO Silveira, Marcio AP Santana, Isabella G Ribeiro, Daniel G Chaves and Olindo A Martins-Filho
    Citation: BMC Hematology 2015 15:1
  10. Ethiopia is one of the most seriously HIV affected countries in Sub-Saharan Africa. Anemia is a known predictor of disease progression and death among HIV infected patients. In this study, we investigated the ...

    Authors: Muluken Assefa, Woldaregay Erku Abegaz, Aster Shewamare, Girmay Medhin and Mulugeta Belay
    Citation: BMC Hematology 2015 15:6
  11. At the time of diagnosis, Multiple Myeloma is commonly associated with renal impairment. Renal tubular acidosis without overt renal insufficiency is an uncommon disease presentation of myeloma. Among tubular a...

    Authors: Chathuranga Lakmal Fonseka, Sampath Rukshani Galappaththi, Jeewandarage Dhanushka Karunarathna, Dayakshi Dushyantha Kumarihami Abeyaratne and Nirmali Tissera
    Citation: BMC Hematology 2016 16:8
  12. It has been reported that patients with SCD do have an abnormal coagulation profile. Coagulopathy is thought to be one of the key factors that contribute to the vaso-occlusive crisis that characterises sickle ...

    Authors: Shiekh Awoda, Ahmed A. Daak, Nazik Elmalaika Husain, Kebreab Ghebremeskel and Mustafa I. Elbashir
    Citation: BMC Hematology 2017 17:18
  13. Anemia is a strong predictor of mortality and poor quality of life among persons with either renal impairment or HIV infection. In this study, we investigated the prevalence of anemia and its association with ...

    Authors: Temesgen Fiseha, Zemenu Tamir, Abdurahaman Seid and Wondmagegn Demsiss
    Citation: BMC Hematology 2017 17:1
  14. Chromosomal abnormalities are diagnostic and prognostic key factors in acute myeloid leukemia (AML) patients, as they play a central role for risk stratification algorithms. High hyperdiploidy (HH), a rare cyt...

    Authors: Abdulsamad Wafa, Suher ALmedania, Abdulmunim Aljapawe, Thomas Liehr, Soulaiman E. Soulaiman, Raja Mouna, Moneeb A. K. Othman and Walid ALachkar
    Citation: BMC Hematology 2018 18:21
  15. A high prevalence of neutropenia has been reported in several ethnic groups amongst whom many healthy individuals with low neutrophil counts undergo unnecessary investigations. This study aims to ascertain the...

    Authors: Srdjan Denic, Hassib Narchi, Lolowa A. Al Mekaini, Suleiman Al-Hammadi, Omar N. Al Jabri and Abdul-Kader Souid
    Citation: BMC Hematology 2016 16:15
  16. Africa is the most affected continent with 200,000 new born affected by sickle cell anemia annually with of 5% of under five deaths. Nigeria has the largest sickle cell gene pool in the world with about 2% of ...

    Authors: Olorunfemi Emmanuel Amoran, Ahmed Babatunde Jimoh, Omotola Ojo and Temitope Kuponiyi
    Citation: BMC Hematology 2017 17:6
  17. Familial and acquired thrombophilia are often etiologic for idiopathic hip and jaw osteonecrosis (ON), and testosterone therapy (TT) can interact with thrombophilia, worsening ON.

    Authors: Michael Ian Jarman, Kevin Lee, Ariel Kanevsky, Sarah Min, Ilana Schlam, Chris Mahida, Ali Huda, Alexander Milgrom, Naila Goldenberg, Charles J. Glueck and Ping Wang
    Citation: BMC Hematology 2017 17:5
  18. Anemia is the most common hematological abnormality in Human immunodeficiency virus (HIV) positive patients and a significant predictor of its progression to AIDS or death. This study was aimed to assess the p...

    Authors: Gashaw Garedew Woldeamanuel and Diresibachew Haile Wondimu
    Citation: BMC Hematology 2018 18:7
  19. Idiopathic (immune) thrombocytopenic purpura (ITP) is an acquired disorder characterized by autoantibodies against platelet membrane antigens. Several studies found an association between Helicobacter Pylori i...

    Authors: Sara Aljarad, Ahmad Alhamid, Ahmad Sankari Tarabishi, Ameen Suliman and Ziad Aljarad
    Citation: BMC Hematology 2018 18:28

    The Correction to this article has been published in BMC Hematology 2019 19:11

  20. Anemia in pregnancy may not only be associated with maternal morbidity and mortality but can also be detrimental to the fetus. A definitive diagnosis of anemia is a pre-requisite to unravelling possible cause(...

    Authors: Benjamin Ahenkorah, Kwabena Nsiah, Peter Baffoe and Enoch Odame Anto
    Citation: BMC Hematology 2018 18:27
  21. Iron deficiency anemia is highly prevalent in patients with chronic kidney disease and is often treated with intravenous iron. There are few trials directly comparing the safety and efficacy of different intra...

    Authors: William E. Strauss, Naomi V. Dahl, Zhu Li, Gloria Lau and Lee F. Allen
    Citation: BMC Hematology 2016 16:20
  22. Although a state of anemia is perceived to be associated with spaceflight, to date a peripheral blood hematologic assessment of red blood cell (RBC) indices has not been performed during long-duration space mi...

    Authors: Hawley Kunz, Heather Quiriarte, Richard J. Simpson, Robert Ploutz-Snyder, Kathleen McMonigal, Clarence Sams and Brian Crucian
    Citation: BMC Hematology 2017 17:12
  23. Massive bleeding is one of the commonest salvageable causes of death. The search for an ideal haemostatic agent during massive bleeding is still ongoing. One of the novel haemostatic medications is recombinant...

    Authors: Nurfatin Mohd Shah, Soon Eu Chong, Syahirah Mohamed Yusoff, Mohd Zulfakar Mazlan, Khairul Bariah Johan, Nizuwan Azman, Jo Anne Lim, Siti Mardhiana Mohamad, Siti Salmah Noordin, Zainab Abdul Ghaffar, Mohd Hasyizan Hassan, Muhammad Azrul Zabidi and Nur Arzuar Abdul Rahim
    Citation: BMC Hematology 2018 18:34
  24. Tumor lysis syndrome (TLS) is a life-threatening emergency disorder, caused by an abrupt release of intracellular metabolites after tumor cell death. It is characterized by a series of metabolic manifestations...

    Authors: Haileleul Micho, Yasin Mohammed, Daniel Hailu and Solomon Genet
    Citation: BMC Hematology 2018 18:22
  25. Despite the public health significance of anaemia in African children, its broader and often preventable risk factors remain largely under described. This study investigated, for the first time, the prevalence...

    Authors: Ismail Dragon Legason, Alex Atiku, Ronald Ssenyonga, Peter Olupot-Olupot and John Banson Barugahare
    Citation: BMC Hematology 2017 17:10
  26. Since the discovery of specific histocompatibility, literature has associated genes involved in the immune response, like the Human Leucocyte Antigen (HLA), with a better prognosis in transplantation. However,...

    Authors: Daniele Kazue Sugioka, Carlos Eduardo Ibaldo Gonçalves and Maria da Graça Bicalho
    Citation: BMC Hematology 2016 16:25
  27. In this study, we evaluate the association of different clinical profiles, laboratory and genetic biomarkers in patients with sickle cell anemia (SCA) and hemoglobin SC disease (HbSC) in attempt to characteriz...

    Authors: Milena Magalhães Aleluia, Teresa Cristina Cardoso Fonseca, Regiana Quinto Souza, Fábia Idalina Neves, Caroline Conceição da Guarda, Rayra Pereira Santiago, Bruna Laís Almeida Cunha, Camylla Villas Boas Figueiredo, Sânzio Silva Santana, Silvana Sousa da Paz, Júnia Raquel Dutra Ferreira, Bruno Antônio Veloso Cerqueira and Marilda de Souza Gonçalves
    Citation: BMC Hematology 2017 17:15
  28. Tuberculosis (TB) treatment may present significant hematological disorder and some anti-TB drugs also have serious side effects. Although many other diseases may be reflected by the blood and its constituents...

    Authors: Eyuel Kassa, Bamlaku Enawgaw, Aschalew Gelaw and Baye Gelaw
    Citation: BMC Hematology 2016 16:1
  29. Anemia affects a significant part of the population in nearly every country in the globe. Iron requirements are greatest at ages 6–23 months when growth is extremely rapid and critically essential in critical ...

    Authors: Bereket Geze Malako, Melese Sinaga Teshome and Tefera Belachew
    Citation: BMC Hematology 2018 18:14
  30. Fibrin provides a temporary matrix at the site of vascular injury. The aims of the present work were (1) to follow fibrin formation and lysis onto the surface of human dermal microvascular endothelial cells (H...

    Authors: O. Castillo, H. Rojas, Z. Domínguez, E. Anglés-Cano and R. Marchi
    Citation: BMC Hematology 2016 16:9
  31. Active and passive theories have been advanced to explain splenomegaly and cytopenias in liver disease. Dameshek proposed active downregulation of hematopoiesis. Doan proposed passive trapping of blood compone...

    Authors: John M. Gemery, Andrew R. Forauer, Anne M. Silas and Eric K. Hoffer
    Citation: BMC Hematology 2016 16:3
  32. Anemia is a significant wide spread public health threat especially among the adolescent girls who are more vulnerable towards low level of hemoglobin particularly of low and middle income countries (LMICs). W...

    Authors: Sabuj Kanti Mistry, Fatema Tuz Jhohura, Fouzia Khanam, Fahmida Akter, Safayet Khan, Fakir Md Yunus, Md Belal Hossain, Kaosar Afsana, Md Raisul Haque and Mahfuzar Rahman
    Citation: BMC Hematology 2017 17:13
  33. Anemia is a common hematologic disorder among human Immunodeficiency virus (HIV) infected adult Individuals. However, there is no concrete scientific evidence established at national level in Ethiopia. Hence, ...

    Authors: Ayenew Negesse, Temesgen Getaneh, Habtamu Temesgen, Tesfahun Taddege, Dube Jara and Zeleke Abebaw
    Citation: BMC Hematology 2018 18:32
  34. Evidence-based guidelines for sickle cell disease (SCD) health maintenance and management have been developed for primary health care providers, but not for individuals with SCD. To improve the quality of care...

    Authors: Robert Michael Cronin, Tilicia L. Mayo-Gamble, Sarah-Jo Stimpson, Sherif M. Badawy, Lori E. Crosby, Jeannie Byrd, Emmanuel J. Volanakis, Adetola A. Kassim, Jean L. Raphael, Velma M. Murry and Michael R. DeBaun
    Citation: BMC Hematology 2018 18:12
  35. Africa has the highest burden of Sickle cell disease (SCD) but there are few large, systematic studies providing reliable descriptions of the disease spectrum. Tanzania, with 11,000 SCD births annually, establ...

    Authors: Julie Makani, Furahini Tluway, Abel Makubi, Deogratius Soka, Siana Nkya, Raphael Sangeda, Josephine Mgaya, Stella Rwezaula, Fenella J. Kirkham, Christina Kindole, Elisha Osati, Elineema Meda, Robert W. Snow, Charles R. Newton, David Roberts, Muhsin Aboud…
    Citation: BMC Hematology 2018 18:33
  36. Multiple myeloma is a plasma cell tumour with an annual incidence in the UK of approximately 40–50 per million i.e. about 4500 new cases per annum. The triple combination cyclophosphamide, bortezomib (Velcade®...

    Authors: Sarah Brown, Samantha Hinsley, Mónica Ballesteros, Sue Bourne, Paul McGarry, Debbie Sherratt, Louise Flanagan, Walter Gregory, Jamie Cavenagh, Roger Owen, Cathy Williams, Martin Kaiser, Eric Low and Kwee Yong
    Citation: BMC Hematology 2016 16:14
  37. Transfusion-transmissible infections pose a major health risk in developing countries, including Eritrea. In the present study, we sought to determine the prevalence of specific transfusion transmitted infecti...

    Authors: Yacob Tesfamichael Keleta, Oliver Okoth Achila, Absera Woldu Haile, Bereket Habteslasie Gebrecherkos, Danait Tareke Tesfaldet, Kibrom Solomon Teklu, Mesuda Abrhum Mohammed and Selihom Tesfaslase Ghedel
    Citation: BMC Hematology 2019 19:5
  38. This study was undertaken to explore the longitudinal patterns of health-related quality of life (HRQoL) among youth and young adults with Hemophilia A (HA) over a 3-year period. This report presents the basel...

    Authors: J. St-Louis, D. J. Urajnik, F. Ménard, S. Cloutier, R. J. Klaassen, B. Ritchie, G. E. Rivard, M. Warner, V. Blanchette and N. L. Young
    Citation: BMC Hematology 2016 16:13
  39. Immunophenotypic analysis of the bone marrow (BM) cells has proven to be helpful in the diagnosis of Myelodysplastic Syndromes (MDS). However, the usefulness of flow cytometry (FCM) for the detection of myelod...

    Authors: Ana Aires, Maria dos Anjos Teixeira, Catarina Lau, Cláudia Moreira, Ana Spínola, Alexandra Mota, Inês Freitas, Jorge Coutinho and Margarida Lima
    Citation: BMC Hematology 2018 18:6
  40. CC-486 is an oral formulation of the epigenetic modifier azacitidine. In an expanded phase 1 trial, CC-486 demonstrated clinical and biological activity in patients with International Prognostic Scoring System...

    Authors: Guillermo Garcia-Manero, Antonio Almeida, Aristoteles Giagounidis, Uwe Platzbecker, Regina Garcia, Maria Teresa Voso, Stephen R. Larsen, David Valcarcel, Lewis R. Silverman, Barry Skikne and Valeria Santini
    Citation: BMC Hematology 2016 16:12
  41. Sickle cell disease (SCD) accounts for 5% of mortality in African children aged < 5 years. Improving the care management and quality of life of patients with SCD requires a reliable diagnosis in resource-limit...

    Authors: Akueté Yvon Segbena, Aldiouma Guindo, Romain Buono, Irénée Kueviakoe, Dapa A. Diallo, Gregory Guernec, Mouhoudine Yerima, Pierre Guindo, Emilie Lauressergues, Aude Mondeilh, Valentina Picot and Valériane Leroy
    Citation: BMC Hematology 2018 18:26
  42. Zinc protoporphyrin (ZPP) has been used to screen and manage iron deficiency in individual children, but it has also been recommended to assess population iron status. The diagnostic utility of ZPP used in com...

    Authors: Emily M. Teshome, Andrew M. Prentice, Ayşe Y. Demir, Pauline E.A. Andang’o and Hans Verhoef
    Citation: BMC Hematology 2017 17:11