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ISSN:2688-6146

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IF/分区:1.2/Q4

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共收录本刊相关文章索引1303
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Louise J Potter,Roochi Trikha,Shreyans Gandhi et al. Louise J Potter et al.
A 28-year-old male with paroxysmal nocturnal haemoglobinuria (PNH) presented with headache, nasal bridge discomfort and haemoglobinuria. He developed a macular-papular rash which rapidly progressed into purpura, necrosis and peri-orbital oe...
Sandra M Frey,Ferras Alashkar,H Christian Reinhardt et al. Sandra M Frey et al.
Introduction: Aplastic anemia (AA) is a rare bone marrow failure syndrome with pancytopenia, mainly due to immune-mediated stem cell destruction. First-line therapy for acquired severe AA ≥ 50 years/non-severe AA (NSAA) ...
Mobina Shrestha,Salina Dahal,Asis Shrestha et al. Mobina Shrestha et al.
Background: Older adults with acute myeloid leukemia (AML) have inferior outcomes, yet current genetic risk models do not explicitly account for how age modifies the prognostic impact of molecular features. We hypothesize...
Davide Marcolongo,Alessandra Bressan,Elisabetta Zanatta et al. Davide Marcolongo et al.
Background: Cutaneous monoclonal gammopathy of clinical significance (MGCS) is rare and may present with scleredema-like fibrosing skin disease. Case: ...
Laetitia Largeaud,Charlotte Syrykh,Julie Vial et al. Laetitia Largeaud et al.
Introduction: Histiocytic sarcoma (HS) is a rare neoplasm derived from non-Langerhans histiocytic cells, exceptionally arising from B-ALL. Methods: ...
Akshat Jain,Lisa Roberts,Safiye Sahin Akshat Jain
Introduction: Sickle cell disease (SCD) is a chronic genetic disorder causing severe pain, anemia, and systemic complications that negatively affect patients' physical and mental well-being. The aim of this global cross-s...
Shakirat Gold-Olufadi,Kayode Ogunniyi,Adeleke Oluwaseun Dorcas et al. Shakirat Gold-Olufadi et al.
Introduction: Sickle cell disease (SCD) is a hematologic disorder characterized by chronic hemolysis, vaso-occlusion, and end-organ dysfunction. Patients with SCD may experience acute episodes known as sickle cell crises,...
Xin Kong,Jingjing Han,Yin Liu et al. Xin Kong et al.
Objectives: Studies on the efficacy and safety of haploidentical hematopoietic stem cell transplantation (haplo-SCT) with anti-thymocyte globulin (ATG) in patients aged ≥ 60 years remain limited. ...