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Jurnal

Journal of Applied Hematology

Scopus

ISSN 1658-5127 · Wolters Kluwer Medknow Publications · 546 artikel di indeks

  1. Artikel Jurnal

    Methemoglobinemia with an Oxygen Saturation Gap Secondary to Favism in a Newly Diagnosed Glucose-6-Phosphate Dehydrogenase Deficiency

    Arwa El-Dhuwaib; Deepika Gandhi

    Journal of Applied Hematology, Vol. 17 No. 2 · 2026 · Inggris · DOAJ Scopus

    Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common enzyme deficiency worldwide, with the highest prevalence in African, Asian, and Mediterranean populations, typically presenting with hemolytic anemia. On the other hand, methemoglobinemia is a potentially life-threatening…

  2. Artikel Jurnal

    Red Blood Cell Metabolism in Hemoglobinopathies of Sickle Cell Disorder and Thalassemia Patients in the State of Odisha

    Apratim Sai Rajesh; Atanu Kumar Thakur; Nayan Kumar Patel dkk.

    Journal of Applied Hematology, Vol. 17 No. 2 · 2026 · Inggris · DOAJ Scopus

    BACKGROUND: Hemoglobinopathies are highly prevalent in Odisha, India and are associated with red blood cell (RBC) physiology through chronic hemolysis, oxidative stress, and altered energy metabolism. However, data on RBC glucose metabolism and redox status on hemoglobin variants are limited. AIMS…

  3. Artikel Jurnal

    ABO and Rh Blood Groups Association with Hemoglobin and Serum Ferritin Levels in Patients with Iron Deficiency Anemia: A Cross-Sectional Study

    Hanan B. Saadon

    Journal of Applied Hematology, Vol. 17 No. 2 · 2026 · Inggris · DOAJ Scopus

    BACKGROUND: Iron-deficiency anemia (IDA) is a common and widespread disease; but the role of blood groups ABO and Rh in affecting haemoglobin (Hb) and ferritin is unclear and has yet to be found. OBJECTIVE: To explore the relationship between ABO and Rh blood group systems and serum Hb and ferritin…

  4. Artikel Jurnal

    Case Report of Severe Clostridium difficile Infection Presenting with Incidental Finding of Isolated Pulmonary Embolism

    Wafa Alnofal

    Journal of Applied Hematology, Vol. 17 No. 2 · 2026 · Inggris · DOAJ Scopus

    Clostridium difficile infection is a leading cause of healthcare-associated diarrhea with significant morbidity and mortality, particularly in immunocompromised and elderly patients. Due to inflammation-induced hypercoagulability and depletion of anticoagulant proteins, emerging links to…

  5. Artikel Jurnal

    Prevalence of Stroke and Outcome in Relation to Risk Factors and Comorbidities in Children with Sickle Cell Disease

    Rehab Alluqmani; Fawaz Al-Kasim; Fauzia R Azmet dkk.

    Journal of Applied Hematology, Vol. 17 No. 2 · 2026 · Inggris · DOAJ Scopus

    BACKGROUND: Stroke is a major cause of morbidity in children with sickle cell disease (SCD). We aimed to characterize clinical and demographic features, risk factors, and outcomes of pediatric SCD patients who developed stroke at a tertiary center in Saudi Arabia. METHODOLOGY: We conducted a…

  6. Artikel Jurnal

    A 2-year Review of Hemoglobinopathies using High-performance Liquid Chromatography at a Single Tertiary Center in Baghdad, Iraq

    Taif Ali Khaleel Al-Attafi; Mustafa Jasim Alwan; Husham Raad Abbas dkk.

    Journal of Applied Hematology, Vol. 17 No. 2 · 2026 · Inggris · DOAJ Scopus

    BACKGROUND: Hemoglobinopathies are among the most common inherited disorders worldwide and represent a significant health burden in Iraq. High-performance liquid chromatography (HPLC) is considered a reliable and fast method for screening and diagnosis of β-thalassemia and hemoglobin variants. This…

  7. Artikel Jurnal

    Predictive Utility of a Noninvasive Serum Biomarker Panel for the Diagnosis of Myelodysplastic Syndrome

    Teeb M. Jaafar Al-Khafaji; Mohammed Ali Al-Jabory; Liqaa Mohammed Al-Sharifi

    Journal of Applied Hematology, Vol. 17 No. 2 · 2026 · Inggris · DOAJ Scopus

    BACKGROUND: Myelodysplastic syndrome (MDS) is a clonal hematopoietic stem cell disorder that predominantly affects the elderly and is characterized by bone marrow dysplasticity and cytopenia of the peripheral blood. Prompt and accurate diagnosis is essential for effective management and improvement…

  8. Artikel Jurnal

    Pediatric Familial Erythrocytosis Type 2 due to a Homozygous von Hippel–Lindau Variant Presenting with Cerebral Infarcts

    Sagar Venkatesh; Usha Bangalore Kantharajanna; Dhanalakshmi Kumble dkk.

    Journal of Applied Hematology, Vol. 17 No. 2 · 2026 · Inggris · DOAJ Scopus

    Familial erythrocytosis type 2 (ECYT2), also known as Chuvash polycythemia, is a rare autosomal recessive disorder caused by pathogenic variants in the von Hippel–Lindau (VHL) gene, resulting in dysregulated oxygen sensing and increased erythropoietin (EPO) production. Pediatric cases are uncommon…

  9. Artikel Jurnal

    Effect of Interleukin 6 Levels on Allogeneic Stem Cell Transplantation

    Ahmet Kaya; Mehmet Ali Erkurt; Irfan Kuku dkk.

    Journal of Applied Hematology, Vol. 17 No. 2 · 2026 · Inggris · DOAJ Scopus

    BACKGROUND: Interleukin (IL)-6 has been shown to be an inducer of the acute phase response and to play a role in the pathogenesis of several diseases, including graft versus host disease (GVHD) after allogeneic hematopoietic stem cell transplantation (HSCT). MATERIALS AND METHODS: The relationship…

  10. Artikel Jurnal

    Revisiting the “1 g/dL Rule:” Physiological Variability in Hemoglobin Increment after Single-Unit Red Blood Cell Transfusion

    Ritika Agarkar; Rudraksh Kesharwani; Shubhangi Nagpal dkk.

    Journal of Applied Hematology, Vol. 17 No. 2 · 2026 · Inggris · DOAJ Scopus

    BACKGROUND: Red blood cell (RBC) transfusion is commonly expected to increase hemoglobin concentration by approximately 1 g/dL/unit transfused. However, considerable variability in posttransfusion hemoglobin response is observed in routine clinical practice. Understanding the physiological factors…

  11. Artikel Jurnal

    Serum Cytokeratin-18 as a Noninvasive Biomarker of Hepatocellular Injury in Patients with β-thalassemia

    Hussein Yusuf Khanyab; Ihsan Shakir Mahmood; Enass Abdul Kareem Dagher

    Journal of Applied Hematology, Vol. 17 No. 2 · 2026 · Inggris · DOAJ Scopus

    BACKGROUND: Chronic transfusion therapy in β-thalassemia causes progressive iron overload and oxidative hepatocellular injury. Conventional markers, such as serum ferritin and aminotransferases, are limited by their lack of specificity, highlighting the need for reliable, noninvasive biomarkers of…

  12. Artikel Jurnal

    Biochemical and Statistical Predictors of Iron-deficiency Anemia among Patients with Normochromic Normocytic Anemia

    Farah A. Mohammed; Ola Salah Qasim Zoori; Rusul Najah Abdulkadhim

    Journal of Applied Hematology, Vol. 17 No. 2 · 2026 · Inggris · DOAJ Scopus

    BACKGROUND: The chronic illness anemia is often mild-to-moderate normocytic normochromic anemia, which changes with time to become hypochromic or microcytic. OBJECTIVE: The objective of this study was to identify the biochemical and statistical predictors of iron-deficiency anemia (IDA) among…

  13. Artikel Jurnal

    Assessing Iron-deficiency Anemia among Female University Students in a Single Center

    Hind AlHumaidan; Wasaef Alharbi; Ayomi Jayathilake dkk.

    Journal of Applied Hematology, Vol. 17 No. 2 · 2026 · Inggris · DOAJ Scopus

    BACKGROUND: Gynecological and nutritional factors are key contributors to the development of iron deficiency anemia (IDA) in women. OBJECTIVE: This study was conducted to assess IDA among female university students in Saudi Arabia. DESIGN: Cross-sectional study. SETTING: University. PATIENTS AND…

  14. Artikel Jurnal

    B-cell Maturation Antigen-directed Therapies versus Standard Regimens in Lenalidomide-refractory Relapsed or Refractory Multiple Myeloma After 1-3 Prior Lines: A Systematic Review and Network Meta-analysis of Phase 3 Trials

    Carlos Camargo; Carlos A. Corona-Arias; Yeimy Carolina Chaparro Sandoval dkk.

    Journal of Applied Hematology, Vol. 17 No. 2 · 2026 · Inggris · DOAJ Scopus

    The therapeutic landscape for relapsed or refractory multiple myeloma (RRMM) has evolved with the introduction of B-cell maturation antigen (BCMA)-directed agents and novel triplet combinations; however, robust comparative evidence in lenalidomide-refractory patients with early relapse remains…

  15. Artikel Jurnal

    The Correlation between Helicobacter pylori Chronic Gastritis in Adults and Anemia in GIT Center in Baghdad City

    Sarab Hesham Moulod; Nada H. A. Al-Mudallal

    Journal of Applied Hematology, Vol. 17 No. 2 · 2026 · Inggris · DOAJ Scopus

    BACKGROUND: Helicobacter pylori is a widespread gastric bacterium that is linked to ulcers, chronic gastritis, and iron deficiency anemia (IDA); this paper examines its connection with anemia and determines the diagnostic value of histopathological biopsy in patients with a Baghdad GIT Center in…

  16. Artikel Jurnal

    Clinical Safety and Legal Accountability of Artificial Intelligence in Hematology Diagnostic Laboratories: Risks, Failure Modes, Medicolegal Challenges, and Budgeting for Implementation

    Asaad Ma. Babker

    Journal of Applied Hematology, Vol. 17 No. 2 · 2026 · Inggris · DOAJ Scopus

    BACKGROUND: Artificial intelligence (AI) is increasingly embedded in hematology diagnostic laboratories, where it supports blood smear interpretation, flow cytometry, genomic analysis, and clinical decision support. While these tools can enhance efficiency and diagnostic accuracy, their deployment…

  17. Artikel Jurnal

    Cancer-associated Microangiopathic Hemolytic Anemia in Lung Adenocarcinoma with Bone Marrow Metastasis

    Majed Abdul Basit Momin

    Journal of Applied Hematology, Vol. 17 No. 1 · 2026 · Inggris · DOAJ Scopus

    A 60-year-old woman with previous lung adenocarcinoma had bicytopenia and fragmented red blood cells (schistocytes) on a peripheral blood smear, indicating microangiopathic hemolytic anemia (MAHA). A bone marrow biopsy revealed metastatic adenocarcinoma. The identification of cancer-associated MAHA…

  18. Artikel Jurnal

    Data Driven Prediction of EuroQol Five-dimension Five-level Outcomes in Hemophilia through Algorithmic Modeling of Quality of Life

    Nitya Krishnasamy; K. Hema Shree; Sameep Shetty dkk.

    Journal of Applied Hematology, Vol. 17 No. 1 · 2026 · Inggris · DOAJ Scopus

    BACKGROUND: Hemophilia is an inherited X-linked bleeding disorder, characterized by the deficiency of coagulation factor VIII (hemophilia A) or factor IX (hemophilia B), leading to recurrent bleeding, chronic joint damage, and functional impairment. Beyond clinical manifestations, hemophilia…

  19. Artikel Jurnal

    Hematological Abnormalities among Pediatric Patients with Helicobacter pylori Infection: A Retrospective Study from Jazan, Saudi Arabia

    Abdulmalik A. Najmi; Mohammed Y. Suhaqi; Salihah M. Ghazwani dkk.

    Journal of Applied Hematology, Vol. 17 No. 1 · 2026 · Inggris · DOAJ Scopus

    OBJECTIVES: To describe hematological abnormalities, particularly anemia and related red blood cell indices, among pediatric patients with biopsy-confirmed Helicobacter pylori infection. METHODS: A retrospective, single-center, and cross-sectional study was conducted at King Fahad Central Hospital…