• A case of adrenal Castleman disease combined with liver cirrhosis and splenomegaly
• A case report of hemophagocytic lymphohistiocytosis induced by toripalimab plus chemoradiotherapy in cervical cancer
• A diagnostic dilemma: distinguishing a sulfasalazine induced DRESS hypersensitivity syndrome from a CD30 + lymphoma in a young patient
• A Novel Frameshift Mutation of <em>HBB</em> Causing Dominant β-Thalassemia in a Chinese Individual
• A patient-based murine model recapitulates human STAT3 gain-of-function syndrome
• A Rare Case of Bone Marrow Sarcoidosis
• A rare case report of splenic infarction in a previously healthy teenager caused by acute infectious mononucleosis
• A rare differential diagnosis of inflammatory bowel disease in a young male patient; a challenging case report
• A Real Gut Punch: An Unexpected Diagnosis of Spontaneous Splenic Rupture
• A Stellar Case of Splenic Hydatid Cyst
• Acute splenic pathology on CT in patients with babesiosis
• Aleukemic variant of T-cell large granular lymphocyte leukemia in patients with rheumatoid arthritis - diagnostically challenging subtype
• Allogeneic stem cell transplant in primary hemophagocytic lymphohistiocytosis - a single-center experience
• Association Between Diagnostic Delays and Spinal Involvement in Human Brucellosis: A Retrospective Case-Control Study
• Asymptomatic cirrhosis in a 35-year-old female
• Atypical presentation of Felty syndrome: Successful management with rituximab therapy-A case report and review of literature
• Autoimmune hepatitis presenting as severe anemia
• Berberine HCl and diacerein loaded dual delivery transferosomes: Formulation and optimization using Box-Behnken design
• Beyond the Usual Suspects: Unraveling Spleen Mastocytosis in Hypersplenism Differential Diagnosis
• Characteristics of large granular lymphocyte leukemia associated with variable common immunodeficiency disorders: A study of 12 cases
• Clinical features and prognostic factors of advanced myelodysplastic syndromes in children
• Clinical features of blastic plasmacytoid dendritic neoplasm in Chile: report of 10 cases
• Clinical Features of Cytokine Storm Syndrome
• Clinical Validation of the Somatic FANCD2 Mutation (c.2022-5C&gt;T) as a Novel Molecular Biomarker for Early Disease Progression in Chronic Myeloid Leukemia: A Case-Control Study
• Combination Therapy with Ruxolitinib and Pegylated Interferon-alpha2a in Newly Diagnosed Patients with Polycythemia Vera
• Comorbidities and complications in adult and paediatric patients with pyruvate kinase deficiency: Analysis from the Peak Registry
• Computed Tomography Finding of Crusty Thrombosed Arteries: An Appearance of Lower Extremity Vascular Pythiosis
• Concurrent squamous cell carcinoma and non-hodgkin lymphoma: a rare case report and multidisciplinary approach
• Congenital Cytomegalovirus in a Resource-Limited Setting: A Case Report
• Cumulative Donor-Specific Antibody Threshold Predicts Platelet Transfusion Response in HLA-Alloimmunized Patients
• Cytokine Storm Syndrome as a Manifestation of Primary HIV Infection
• DARS expression in BCR/ABL1-negative myeloproliferative neoplasms and its association with the immune microenvironment
• Deletion of the Mitochondrial Membrane Protein Fam210b Is Associated with the Development of Systemic Lupus Erythematosus
• Detection of HbD Punjab Trait in Saurashtra Region of Gujarat by HPLC Method
• Development and validation of a nomogram based on Lasso-Logistic regression for predicting splenomegaly secondary to acute pancreatitis
• Diagnostic Detection of H7N3 Low Pathogenicity Avian Influenza in a Commercial Game Bird Flock
• Does a subset of mature T-cell leukemias with features akin to T-cell prolymphocytic leukemia but lacking rearrangement of the <em>TCL1</em> represent peripheral T-cell lymphoma, NOS in a leukemic phase?
• Effective Prevention and Treatment of Acute Leukemias in Mice by Activation of Thermogenic Adipose Tissues
• Effects of Jianpi Huayu Decoction on Th1/Th2 Immune Balance in Mice With Liver Cancer-Related Fatigue via the IL- 27/STAT1 Signaling Pathway
• Etiologies of Splenic Venous Hypertension: A Review
• Evaluating the Impact of Low-Pathogenicity Avian Influenza H6N1 Outbreaks in United Kingdom and Republic of Ireland Poultry Farms during 2020
• Evolution of splenomegaly in liver cirrhosis: simulation using an electronic circuit
• Extramedullary Paravertebral Mass: An Unusual Presentation of Hairy Cell Leukaemia
• Factors associated with signs of congenital syphilis in newborns
• Familial Hemophagocytic Lymphohistiocytosis Screening in Neonatal Sepsis
• FRACTION: protocol of a phase II study of Fedratinib and Nivolumab combination in patients with myelofibrosis and resistance or suboptimal response to JAK-inhibitor treatment of the German MPN study group (GSG-MPN)
• Further Clinical Delineation of Prolidase Deficiency Associated with c.1103T&gt;G Variant
• Gamma-delta T-cell large granular lymphocytic leukemia in the setting of rheumatologic diseases
• Genetic Testing in Patients with Autoimmune Lymphoproliferative Syndrome: Experience of 802 Patients at Cincinnati Children's Hospital Medical Center
• Haemophagocytic lymphohistiocytosis (HLH) secondary to disseminated histoplasmosis infection in a patient with HIV
• Hepatic Sinusoidal Disorders
• Hepatic Veno-Occlusive Disease and Colorectal Cancer: Expect the Unexpected
• Histoplasmosis in a fingolimod-treated patient: case report and scoping review
• Hyperimmune malarial splenomegaly in a malaria-endemic area of southwest Burkina Faso: case of Bobo-Dioulasso
• Identification of Risk Factors for Relapse in Childhood Leukemia Using Penalized Semi-parametric Mixture Cure Competing Risks Model
• Identifying disease-modifying potential in myelofibrosis clinical trials
• Infection-associated hemophagocytic lymphohistiocytosis: a case report
• Infective endocarditis in HIV-infected patients. Analysis of a national cohort
• Initial Respiratory System Involvement in Juvenile Idiopathic Arthritis with Systemic Onset Is a Marker of Interstitial Lung Disease: The Results of Retrospective Cohort Study Analysis
• IRAK4 is an immunological checkpoint in neuropsychiatric systemic lupus erythematosus
• Leishmania donovani infection mimicking ulcerative colitis in an immuno-competent patient
• Lessons learned from follow up of spleen-preserving distal pancreatectomy with artery saving and vein sacrificing
• Lymphopenia in the Adult Population With Fontan Physiology: A Potential New Marker for Disease Assessment
• Momelotinib - a promising advancement in the management of myelofibrosis in adults with anemia
• Momelotinib versus ruxolitinib in JAK inhibitor-naïve patients with myelofibrosis: an efficacy/safety analysis in the Japanese subgroup of the phase 3 randomized SIMPLIFY-1 trial
• MoReLife - real-life data support the potential of momelotinib as a safe and effective treatment option for cytopenic myelofibrosis patients
• Myelofibrosis and anemia: A German claims data analysis to describe epidemiology and current treatment
• Natural disease course of chronic visceral acid sphingomyelinase deficiency in adults: A first step toward treatment criteria
• Navigating Portal Hypertension and Splenomegaly: A Clinical Encounter With an Unusual Variant of Cruveilhier-Baumgarten Syndrome
• Non-random distribution of Plasmodium Species infections and associated clinical features in children in the lake Victoria region, Kenya, 2012-2018
• Outbreak of <em>Chlamydia psittaci</em> Infection in a Commercial Psittacine Breeding Aviary in Argentina
• Pathogenesis of Experimental Infection of Nile Tilapia (Oreochromis niloticus) with Nucleospora Braziliensis Pathology and Proteomic of Microsporidia
• Pattern of Clinical Presentation in Patients With Lymphoma
• Point Shear Wave Elastography for Splenic Assessment: A Comparative Study of Splenomegaly and Normal Spleens
• Poorly Controlled New-Onset Diabetes Mellitus and Other Atypical Signs as an Early Sign of Pancreatic Adenocarcinoma
• Quantifying and visualizing abdominal hemodynamics in patients with Fontan circulation by 4D phase-contrast flow magnetic resonance imaging at 1.5 T
• Sarcoidosis presenting as isolated massive splenomegaly: A case report
• Solitary splenic neoplasm as an unusual presentation in an adolescent with sporadic Burkitt lymphoma
• Spinal extramedullary hematopoiesis mimicking an epidural tumor in a patient with high-risk polycythemia vera: illustrative case
• Splenectomy as definitive surgical treatment for hemophagocytic lymphohistiocytosis
• Splenectomy in Thalassemia: The Role of Surgery as an Adjunct to Medical Management
• Splenic abscess secondary to COVID-19 acute infection: A case report and literature review
• Splenic complications in pediatric sickle cell disease: A retrospective cohort review
• Splenomegaly and Response to Splenectomy in Immune Thrombocytopenia
• Still's Disease Onset in Older Adults: Clinical Features, Diagnosis, and Management
• Survival and Disease Progression in Older Adult Patients With Cirrhosis: A Retrospective Study
• Systemic autoinflammatory disease, IgA glomerulonephritis and renal cortical necrosis: coincidence or causation?
• Systemic Lupus Erythematosus and Cytokine Storm
• The assessment of health-related quality of life in patients with polycythemia vera
• The clinical and immunological characteristics of common variable immunodeficiency in adults and older adults
• The clinical picture of Castleman disease-a systematic review and meta-analysis
• Treatment outcomes between cyclosporin and chemotherapy in adult subcutaneous panniculitis-like T-cell lymphoma: a report from nation-wide Thai lymphoma study group registry
• Unlocking milk thistle's anti-psoriatic potential in mice: Targeting PI3K/AKT/mTOR and KEAP1/NRF2/NF-κB pathways to modulate inflammation and oxidative stress
• Unveiling Neglected Concerns: Possible Severe Hepatic Complications after Nephrectomy in Autosomal Dominant Polycystic Kidney Disease - A Case Report
• Update on ocular manifestations of the main monogenic and polygenic autoinflammatory diseases
• Utilization of a Single-Site Port as an Adjunct for Multi-Port Robotic-Assisted Surgery in Children
• Valoctocogene roxaparvovec gene therapy provides durable haemostatic control for up to 7 years for haemophilia A
• Venetoclax combined with azacitidine in blastic plasmacytoid dendritic cell neoplasm: a case report and comprehensive review on the current and future treatment
• Visceral Leishmaniasis: A Case Confirmed by Metagenomic Next-Generation Sequencing from Northwestern China
• Vitamin B12 Deficiency Manifesting As Pancytopenia, Lymphadenopathy, and Fever: A Clinical Mimic of Hematologic Malignancies