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• An unusual cause of anemia and encephalopathy

  Sanjeev Kumar Sharma, Dharma Choudhary, Anil Handoo, Gaurav Dhamija, Gaurav Kharya, Vipin Khandelwal, Mayank Dhamija, Sweta Kothari

  e2015036

  2015-04-24

  https://doi.org/10.4084/mjhid.2015.036

  4125

  PDF: 887

  HTML: 1537

• Life-threatening autoimmune hemolytic anemia and idiopathic thrombocytopenic purpura: successful seletive splenic artery embolization

  matteo molica, Fulvio Massaro, Giorgia Annechini, Erminia Baldacci, Gianna maria D'elia, Riccardo Rosati, Silvia maria trisolini, Paola Volpicelli, Robin Foà, Saveria Capria

  e2016020

  2016-04-10

  https://doi.org/10.4084/mjhid.2016.020

  3676

  PDF: 1037

  HTML: 2367

• A CASE OF CONGENITAL DYSERYTHROPOIETIC ANEMIA MASKED BY HEMOGLOBIN H DISEASE

  Xiaolin Yin

  e2024059

  2024-06-29

  https://doi.org/10.4084/MJHID.2024.059

  788

  PDF: 894

  HTML: 118

• MYELODYSPLASTIC SYNDROMES AND IRON CHELATION THERAPY

  Emanuele Angelucci, Silvana Anna Maria Urru, Federica Pilo, Alberto Piperno

  e2017021

  2017-03-01

  https://doi.org/10.4084/mjhid.2017.021

  3771

  PDF: 1338

  HTML: 2167

  Fig.1: 236

  Fig. 2: 230

• PREDISPOSING FACTORS TO INFECTIONS IN THALASSEMIA SYNDROME PATIENTS

  Eman M Mansory, Lina M. Abdulrahman, Balsam Osman, Sawsan M. Sawsan, Assil F. Ruckn, Marwa Aljedaani, Nemmat Hassan, Ahmed S. Barefah, Hatem M. Alahwal, Yassir Daghistani, Salem M. Bahashwan, Abdullah T. Almohammadi, Osman O. Radhwi

  e2025055

  2025-08-31

  https://doi.org/10.4084/MJHID.2025.055

  1906

  PDF: 1573

  HTML: 497

• INVASIVE FUNGAL INFECTION IN CHILDREN WITH ACUTE LEUKEMIA AND SEVERE APLASTIC ANEMIA IFI in Children with Acute Leukemia and SAA

  Sutatta Supatharawanich, Nattee Narkbunnam, Nassawee Vathana, Chayamon Takpradit, Kamon Phuakpet, Bunchoo Pongtanakul, Sasima Tongsai, Phakatip Sinlapamongkolkul, Popchai Ngamskulrungroj, Wanatpreeya Phongsamart, Kleebsabai Sanpakit , Jassada Buaboonnam

  e2021039

  2021-06-28

  https://doi.org/10.4084/MJHID.2021.039

  2879

  PDF: 942

  HTML: 296

• A novel ALAS2 mutation causes congenital sideroblastic anemia

  Kun Yang

  e2023062

  2023-10-30

  https://doi.org/10.4084/MJHID.2023.062

  774

  PDF: 597

  HTML: 184

• A Rare Case of Rosai-Dorfman Disease in an Adult Male Associated with Auto-immune Hemolytic Anemia.

  Mickey Sachdeva, Haifaa Abdulhaq

  e2013022

  2013-04-10

  https://doi.org/10.4084/mjhid.2013.022

  1444

  PDF: 956

  HTML: 1674

  Figure 1: 195

• GROUP-BASED TRAJECTORY MODELING OF PLATELET IN PATIENTS WITH APLASTIC ANEMIA: A STUDY BASED ON THE MIMIC DATABASE

  Lang Peng, Lixin Zou, Xiaoliu Liu

  e2025012

  2025-02-27

  https://doi.org/10.4084/MJHID.2025.012

  1093

  PDF: 1060

  Suppl. Files: 662

  HTML: 186

• THALIDOMIDE AMELIORATES ERYTHROPOIESIS AND IRON HOMEOSTASIS IN TRANSFUSION-DEPENDENT β-THALASSEMIA Thalidomide ameliorates erythropoiesis and iron homeostasis

  Kun Yang, Jian Xiao

  e2024001

  2024-01-01

  https://doi.org/10.4084/MJHID.2024.001

  1501

  PDF: 1470

  PDF: 1045

  HTML: 231

• USE OF HEMATOPOIETIC GROWTH FACTOR IN THE MANAGEMENT OF HEMATOLOGICAL SIDE EFFECTS ASSOCIATED TO ANTIVIRAL TREATMENT FOR HCV HEPATITIS

  Paola Mancino, Katia Falasca, Claudio Ucciferri, Eligio Pizzigallo, Jacopo Vecchiet

  e2010003

  2010-03-26

  https://doi.org/10.4084/mjhid.2010.003

  1186

  PDF: 554

  HTML: 957

• Microangiopathic Hemolytic Anemia in 57-year-old woman with Borderline Serous Tumor of the Ovary:Real-Time Management of Common Pathways of Hemostatic Failure

  Gloria Joan Morris

  e2012030

  2012-05-06

  https://doi.org/10.4084/mjhid.2012.030

  1284

  PDF: 864

  HTML: 12854

• IRON CHELATION THERAPY WITH DEFERASIROX IN THE MANAGEMENT OF IRON OVERLOAD IN PRIMARY MYELOFIBROSIS

  Elena Maria Elli, Angelo Belotti, Andrea Aroldi, Matteo Parma, Pietro Pioltelli, Enrico Maria Pogliani

  e2014042

  2014-05-30

  https://doi.org/10.4084/mjhid.2014.042

  2214

  PDF: 1195

  HTML: 2017

• Respiratory function in pediatric African SCA patients underwent bone marrow transplantation

  Antonella Isgrò, Javid Gaziev, Marco Marziali, Katia Paciaroni, Gioia De Angelis, Cecilia Alfieri, Michela Ribersani, Festus Olusola Olowoselu, Guido Lucarelli

  e2017030

  2017-04-15

  https://doi.org/10.4084/mjhid.2017.030

  2190

  PDF: 806

  HTML: 1076

  Spirometry in SCA patients before transplant: 229

  Spirometry in SCA patients post transplant: 200

• WALDENSTRÖM MACROGLOBULINEMIA - A STATE-OF-THE-ART REVIEW: PART 1: EPIDEMIOLOGY, PATHOGENESIS, CLINICOPATHOLOGIC CHARACTERISTICS, DIFFERENTIAL DIAGNOSIS, RISK STRATIFICATION, AND CLINICAL PROBLEMS

  Michele Bibas, Shayna Sarosiek, Jorge J. Castillo

  e2024061

  2024-06-29

  https://doi.org/10.4084/MJHID.2024.061

  3083

  PDF: 3343

  HTML: 748

• RECENT ADVANCES IN THE 5Q- SYNDROME

  Andrea Pellagatti, Jacqueline Boultwood

  e2015037

  2015-05-20

  https://doi.org/10.4084/mjhid.2015.037

  2963

  PDF: 1896

  HTML: 3815

  Pellagatti Fig 1: 247

  Pellagatti Fig. 2: 240

• IMPORTANCE OF CLASSICAL MORPHOLOGY IN THE DIAGNOSIS OF MYELODYSPLASTIC SYNDROME

  Rosangela Invernizzi, Federica Quaglia, Matteo Giovanni Della Porta

  e2015035

  2015-04-26

  https://doi.org/10.4084/mjhid.2015.035

  3526

  PDF: 2317

  HTML: 23492

  Untitled: 232

  Untitled: 243

  Untitled: 250

• ACUTE LUNG INJURY COMPLICATING BLOOD TRANSFUSION IN POST-PARTUM HEMORRHAGE: INCIDENCE AND RISK FACTORS.

  Luciana Teofili, Maria Bianchi, Bruno A Zanfini, Stefano Catarci, Rossella Sicuranza, Serena Spartano, Gina Zini, Gaetano Draisci

  e2014069

  2014-10-22

  https://doi.org/10.4084/mjhid.2014.069

  2535

  PDF: 1299

  HTML: 3617

  Acute lung injury complicating blood transfusion in post-partum hemorrhage: incidence and risk factors.: 437

• SERUM TOTAL BILIRUBIN, NOT CHOLELITHIASIS, IS INFLUENCED BY UGT1A1 POLYMORPHISM, ALPHA THALASSEMIA AND ?S GENOTYPE: FIRST REPORT ON COMPARISON BETWEEN ARAB-INDIAN AND AFRICAN ?S GENES

  Said Y ALkindi, Anil Pathare, Salam Alkindi

  e2015060

  2015-10-20

  https://doi.org/10.4084/mjhid.2015.060

  1798

  PDF: 955

  HTML: 1621

• COMPARATIVE EVALUATION OF BONE MARROW ASPIRATE WITH TREPHINE BIOPSY IN HEMATOLOGICAL DISORDERS AND DETERMINATION OF OPTIMUM TREPHINE LENGTH IN LYMPHOMA INFILTRATION

  Surbhi Goyal, Usha Rani Singh, Usha Rusia

  e2014002

  2013-12-31

  https://doi.org/10.4084/mjhid.2014.002

  2087

  PDF: 1109

  HTML: 51889

• MODULATING EFFECT OF THE ?158 G? (C?T) XMN-1 POLYMORPHISM IN INDIAN SICKLE CELL PATIENTS

  Sanjay Pandey, Sweta Pandey, Rahasya Mani Mishra, Renu Saxena

  e2012001

  2012-01-15

  https://doi.org/10.4084/mjhid.2012.001

  1630

  PDF: 930

  HTML: 1446

  Table: 214

• PATHOGENESIS OF MALARIA IN TISSUES AND BLOOD

  Beatrice Autino, Yolanda Corbett, Francesco Castelli, Donatella Taramelli

  e2012061

  2012-10-04

  https://doi.org/10.4084/mjhid.2012.061

  4671

  PDF: 1991

  HTML: 18161

• TREOSULFAN-BASED CONDITIONING REGIMEN IN SIBLING AND ALTERNATIVE DONOR HEMATOPOIETIC STEM CELL TRANSPLANTATION FOR CHILDREN WITH SICKLE CELL DISEASE

  Antonio Marzollo, Elisabetta Calore, Manuela Tumino, Marta Pillon, Maria Vittoria Gazzola, Roberta Destro, Raffaella Colombatti, Piero Marson, Tiziana Tison, Anna Colpo, Chiara Mainardi, Maria Gabelli, Maria Paola Boaro, Sara Rossin, Aurora Strano, Nadia Quaglia, Federica Menzato, Giuseppe Basso, Laura Sainati, Chiara Messina

  e2017014

  2017-02-15

  https://doi.org/10.4084/mjhid.2017.014

  4416

  PDF: 1581

  HTML: 1256

• OUTLINE OF IRON METABOLISM, WITH EMPHASIS TO ERYTHROID CELLS iron Metabolism

  Ugo Testa, Elvira Pelosi, Germana Castelli

  e2025067

  2025-08-31

  https://doi.org/10.4084/MJHID.2025.067

  2390

  PDF: 1179

  Html: 964

• TRANSFUSION PRACTICE, POST-TRANSFUSION COMPLICATIONS AND RISK FACTORS IN SICKLE CELL DISEASE IN SENEGAL, WEST AFRICA.

  Moussa Seck, Alioune Badara Senghor, Mossane Loum, Sokhna Aissatou Touré, Blaise Félix Faye, Alioune Badara Diallo, Mohamed Keita, Elimane Seydi Bousso, Sérigne Mourtalla Guèye, Macoura Gadji, Abibatou Sall, Awa Oumar Touré, Saliou Diop

  e2022004

  2022-01-01

  https://doi.org/10.4084/MJHID.2022.004

  1981

  PDF: 1127

  HTML: 474

• AUTOIMMUNE CYTOPENIAS IN CHRONIC LYMPHOCYTIC LEUKEMIA, FACTS AND MYTHS

  Pavankumar Tandra, Jairam Krishnamurthy, Vijaya Bhatt, Kam Newman, James O Armitage, Mojtaba Akhtari

  e2013068

  2013-11-04

  https://doi.org/10.4084/mjhid.2013.068

  2438

  PDF: 1241

  HTML: 3898

• The INFLUENCE OF NUTRITION ON DISEASE SEVERITY AND HEALTH-RELATED QUALITY OF LIFE IN ADULTS WITH SICKLE CELL DISEASE A Prospective Longitudinal Study

  Sanaa Kamal, Moheyeldeen Mohamed Naghib, Jamaan Al Zahrani, Huda Hassan, Karim Abdel Aziz Moawado, Omar Arrahman

  e2021007

  2021-01-01

  https://doi.org/10.4084/mjhid.2021.007

  2512

  PDF: 992

  HTML: 349

• EARLY PREDICTORS OF RENAL DYSFUNCTION IN ?-THALASSEMIA MAJOR AND INTERMEDIA PATIENTS

  Azza A.G. Tantawy, Nagham El Bablawy, Amira A. M Adly, Fatma S E Ebeid

  e2014057

  2004-09-01

  https://doi.org/10.4084/mjhid.2014.057

  2031

  PDF: 979

  HTML: 3892

• PATHOPHISIOLOGY OF SICKLE CELL DISEASE AND NEW DRUGS FOR THE TREATMENT

  Lucia De Franceschi

  e2009024

  2009-12-26

  1110

  PDF: 671

  HTML: 11185

• INFECTIONS IN THALASSEMIA AND HEMOGLOBINOPATHIES

  Bianca Maria Ricerca, Arturo Di Girolamo, Deborah Rund

  e2009028

  2009-12-28

  1439

  PDF: 654

  HTML: 4456

• PERIOPERATIVE MANAGEMENT OF SICKLE CELL DISEASE: A NARRATIVE REVIEW

  Kwame Ofori Adjepong, Folashade Otegbeye, Yaw Amoateng ADJEPONG

  e2018032

  2018-05-01

  https://doi.org/10.4084/mjhid.2018.032

  10306

  PDF: 3330

  HTML: 1621

• PREVALENCE AND AETIOLOGY OF BACTEREMIA IN FEBRILE CHILDREN WITH SICKLE CELL DISEASE AT A NIGERIA TERTIARY HOSPITAL

  Biobele Jotham Brown, Hannah O Dada-Adegbola, Catherine Trippe, Olufunmilayo Olopade

  e2017039

  2017-06-20

  https://doi.org/10.4084/mjhid.2017.039

  3048

  PDF: 1360

  HTML: 1101

• CARDIAC FUNCTION AND IRON CHELATION IN THALASSEMIA MAJOR AND INTERMEDIA: A REVIEW OF THE UNDERLYING PATHOPHYSIOLOGY AND APPROACH TO CHELATION MANAGEMENT

  Athanasios Aessopos, Vasilios Berdoukas

  e2009002

  2009-07-18

  1647

  PDF: 499

  HTML: 1564

• Congenital Thrombotic Thrombocytopenic Purpura: Atypical Presentation And First ADAMTS 13 Mutation In A Tunisian Child

  aida borgi

  e2013041

  2013-06-03

  https://doi.org/10.4084/mjhid.2013.041

  1208

  PDF: 671

  HTML: 1751

• ALLOIMMUNIZATION IN PATIENTS WITH SICKLE CELL DISEASE AND THALASSAEMIA: EXPERIENCE OF SINGLE CENTRE FROM OMAN

  Anil Pathare, Salam Alkindi

  e2017013

  2017-02-15

  https://doi.org/10.4084/mjhid.2017.013

  2824

  PDF: 1333

  HTML: 1878

• COVID-19-associated cold agglutinin syndrome and hemophagocytic phenomenon in a patient with monoclonal gammopathy of undetermined significance COVID-19-associated cold agglutinin syndrome and hemophagocytic phenomenon

  Kun Yang

  e2025024

  2025-02-27

  https://doi.org/10.4084/MJHID.2025.024

  1189

  PDF: 880

  HTML: 602

• Microangiopathic Anemia of Acute Brucellosis – is it a True TTP?

  Amir Kuperman

  e2010031

  2010-10-01

  https://doi.org/10.4084/mjhid.2010.031

  1244

  PDF: 824

  HTML: 1786

• A PROSPECTIVE STUDY OF BRUCELLOSIS IN CHILDREN: RELATIVE FREQUENCY OF PANCYTOPENIA

  Mohamed El Koumi, Mona Afify, Salha Al-Zahrani

  e2013011

  2013-02-16

  https://doi.org/10.4084/mjhid.2013.011

  2285

  PDF: 877

  HTML: 4033

• Major Artery Occlusion: a Rare Complication of Sickle Cell Disease

  Adnan Agha

  e2010007

  https://doi.org/10.4084/mjhid.2010.007

  1414

  PDF: 1077

  HTML: 4670

• The IMPACT OF SUPEROXIDE DISMUTASE GENETIC POLYMORPHISM (SOD2 VAL16ALA) AND SUPEROXIDE DISMUTASE LEVEL ON DISEASE SEVERITY IN A COHORT OF EGYPTIAN SICKLE CELL DISEASE PATIENTS IN EGYPT SOD and SCD in Egypt

  Mervat Khorshied, Iman A, Shaheen, Yasmeen M.M Selim, Asmaa O. Elshahawy, Ilham Youssry

  e2022037

  2022-04-28

  https://doi.org/10.4084/MJHID.2022.037

  1188

  PDF: 633

  HTML: 499

• Thalassemia carrier detection among pregnant women Thalassemia carrier detection among pregnant women

  Edhyana Sahiratmadja, Merry M.V. Seu, Ita M. Nainggolan, Johanes C. Mose, Ramdan Panigoro

  e2021003

  2021-01-01

  https://doi.org/10.4084/mjhid.2021.003

  2030

  PDF: 696

  HTML: 296

• STUDY OF SERUM HAPTOGLOBIN LEVEL AND ITS RELATION TO ERYTHROPOIETIC ACTIVITY IN BETA THALASSEMIA CHILDREN .

  Seham Ragab, Manal A. Safan, Eman A. Badr

  e2015019

  2015-02-12

  https://doi.org/10.4084/mjhid.2015.019

  2342

  PDF: 1201

  HTML: 2606

  Study of serum haptoglobin level in thalassemia: 384

  Figures: 210

• THE BROAD-RANGING PANORAMA OF SYSTEMIC AUTOINFLAMMATORY DISORDERS WITH SPECIFIC FOCUS ON ACUTE PAINFUL SYMPTOMS AND HEMATOLOGIC MANIFESTATIONS IN CHILDREN

  Donato Rigante

  e2018067

  2018-10-30

  https://doi.org/10.4084/mjhid.2018.067

  2175

  PDF: 1352

  HTML: 1004

• SICKLE CELL DISEASE AND PREGNANCY

  Dipty Jain, Pooja Lodha, Roshan Colah, Prachi Atmapoojya, Prachi Atmapoojya

  e2019040

  2019-06-24

  https://doi.org/10.4084/mjhid.2019.040

  6268

  PDF: 3796

  HTML: 456

• Acute Hemolytic Anemia Following Rasburicase in a Very Late Post-Transplant Relapse of Acute Myeloid Leukemia

  Gianluca Cavallaro, Federico Lussana, Marco Frigeni, Maria Caterina Micò, Alessandra Algarotti, Anna Grassi, Orietta Spinelli, Chiara Pavoni, Elena Oldani, Alessandro Rambaldi

  e2026003

  2026-01-01

  https://doi.org/10.4084/MJHID.2026.003

  661

  PDF: 586

  Html: 246

• Genetic modulators of diversity in biological expression of sickle cell anemia in patients from democratic republic of Congo

  MAMY NGOLE, MAMY NGOLE, GLOIRE MBAYABO, PAUL LUMBALA, VALERIE RACE, NONO MVUAMA, STEPHANIE DEMAN, ERIKA SOUCHE, PROSPER TSHILOBO LUKUSA, CHRIS VAN GEET, KOENRAAD DEVRIENDT, GERT MATTHIJS, AIME LUMAKA, ISABELLE CLEYNEN

  e2025001

  2024-12-31

  https://doi.org/10.4084/MJHID.2025.001

  1971

  HTML: 336

  PDF: 1505

• ADULT SICKLE CELL ANAEMIA PATIENTS IN BONE PAIN CRISIS HAVE ELEVATED PRO-INFLAMMATORY CYTOKINES

  Adekunle Emmanuel Alagbe, John Ayodele Olaniyi, Oladapo Wale Aworanti

  e2018017

  2018-03-01

  https://doi.org/10.4084/mjhid.2018.017

  3051

  PDF: 940

  HTML: 550

• ?-THALASSEMIA DISTRIBUTION IN THE OLD WORLD: A HISTORICAL STANDPOINT OF AN ANCIENT DISEASE

  Vincenzo De Sanctis

  e2017018

  2017-02-20

  https://doi.org/10.4084/mjhid.2017.018

  11558

  PDF: 4451

  HTML: 4887

• THE HEMATOLOGICAL PARAMETERS AND BIOCHEMICAL MARKERS OF IRON STATUS IN ALFA-THALASSEMIA 3.7KB DELETION FROM METROPOLITAN REGION OF MANAUS, AMAZONAS, BRAZIL. alfa-Thalassemia 3.7 deletion From Amazonas, Brazil.

  Fernanda Cozendey Anselmo, Abdou Gafar Soumanou , Cleidiane de Aguiar Ferreira , Flora Maia Viga Sobrinha, Ana Caroline Santos Castro, Rafael Oliveira Brito, Adolfo José Mota, Marilda de Souza Gonçalves, Jose Pereira Moura Neto

  e2021001

  2021-01-01

  https://doi.org/10.4084/MJHID.2021.001

  4228

  PDF: 665

  HTML: 464

• A 9month-old-boy with atypical hemophagocytic lymphohistiocytosis

  Monia Ouederni, MONIA BEN KHALED, Samia Rekaya, Ilhem Ben Fraj, Fethi Mellouli, Mohamed Bejaoui

  e2017057

  2017-10-16

  https://doi.org/10.4084/mjhid.2017.057

  2101

  PDF: 839

  HTML: 1226