Recent advances in the diagnosis and treatment of hemophagocytic lymphohistiocytosis.
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Hemophagocytic lymphohistiocytosis: An unusual complication in disseminated Mycobacterium tuberculosisHematopoietic cell transplantation for hemophagocytic lymphohistiocytosis: recent advances and controversiesCervical lymph node diseases in childrenDevelopment and validation of the HScore, a score for the diagnosis of reactive hemophagocytic syndromeHemophagocytic syndrome with atypical presentation in an adolescent.Clinical characteristics and follow-up analysis of adult-onset Still's disease complicated by hemophagocytic lymphohistiocytosis.Clinical presentation of hemophagocytic lymphohistiocytosis in adults is less typical than in childrenAutoinflammatory periodic fever, immunodeficiency, and thrombocytopenia (PFIT) caused by mutation in actin-regulatory gene WDR1Importance of hyperbilirubinemia in differentiation of primary and secondary hemophagocytic lymphohistiocytosis in pediatric cases.Hemophagocytic Lymphohistiocytosis: an Unusual Complication of Orientia tsutsugamushi Disease (Scrub Typhus)Clinical characteristics and prognostic factors of adult hemophagocytic syndrome patients: a retrospective study of increasing awareness of a disease from a single-center in China.An uncommon presentation of EBV-driven HLH. Primary or secondary? An ongoing dilemmaAcute myeloid leukemia following etoposide therapy for EBV-associated hemophagocytic lymphohistiocytosis: a case report and a brief review of the literature.Expert consensus on dynamics of laboratory tests for diagnosis of macrophage activation syndrome complicating systemic juvenile idiopathic arthritis.Whole-Exome Sequencing Reveals Mutations in Genes Linked to Hemophagocytic Lymphohistiocytosis and Macrophage Activation Syndrome in Fatal Cases of H1N1 Influenza.The risk of hemophagocytic lymphohistiocytosis in Hermansky-Pudlak syndrome type 2The Prognostic Significance of Beta2 Microglobulin in Patients with Hemophagocytic LymphohistiocytosisEvaluation of the plasma micro RNA expression levels in secondary hemophagocytic lymphohistiocytosis.Diagnostic evaluation of patients with suspected haemophagocytic lymphohistiocytosis.Macrophage activation syndrome and cytokine-directed therapies.Hereditary and acquired hemophagocytic lymphohistiocytosis.Pathogenesis of macrophage activation syndrome and potential for cytokine- directed therapies.2016 Classification Criteria for Macrophage Activation Syndrome Complicating Systemic Juvenile Idiopathic Arthritis: A European League Against Rheumatism/American College of Rheumatology/Paediatric Rheumatology International Trials Organisation CollDiagnosing haemophagocytic syndrome.Perforin gene transfer into hematopoietic stem cells improves immune dysregulation in murine models of perforin deficiencyClinical features, treatment, and outcome of macrophage activation syndrome complicating systemic juvenile idiopathic arthritis: a multinational, multicenter study of 362 patients.Fludarabine-based reduced-intensity conditioning regimen for hematopoietic stem cell transplantation in primary hemophagocytic lymphohistiocytosis.[Fever during blood transfusion. A case of coincidence instead of causality].Haemophagocytic lymphohistiocytosis presenting as liver failure following Epstein-Barr and prior hepatitis A infections.Brain damage resembling acute necrotizing encephalopathy as a specific manifestation of haemophagocytic lymphohistiocytosis - induced by hypersensitivity.Clinical significance of lymphocyte subset changes in hemophagocytic lymphohistiocytosis of children.Hemophagocytic lymphohistiocytosis in association with primary cutaneous anaplastic large cell lymphoma.Case of hemophagocytic lymphohistiocytosis with leishmaniasis.Acquired hemophagocytic syndrome: comment to the case report.Adult-onset immunodeficiency--why is it important in rheumatology?Risk of tuberculosis among Alabama children and adolescents treated with tumor necrosis factor inhibitors: a retrospective study.Performance of current guidelines for diagnosis of macrophage activation syndrome complicating systemic juvenile idiopathic arthritis.Rescue of Cytokine Storm Due to HLH by Hemoadsorption in a CTLA4-Deficient Patient.Increase of bone marrow macrophages and CD8+ T lymphocytes predict graft failure after allogeneic bone marrow or cord blood transplantation.A CD57+ CTL Degranulation Assay Effectively Identifies Familial Hemophagocytic Lymphohistiocytosis Type 3 Patients.
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Recent advances in the diagnosis and treatment of hemophagocytic lymphohistiocytosis.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
Recent advances in the diagnosis and treatment of hemophagocytic lymphohistiocytosis.
@ast
Recent advances in the diagnosis and treatment of hemophagocytic lymphohistiocytosis.
@en
type
label
Recent advances in the diagnosis and treatment of hemophagocytic lymphohistiocytosis.
@ast
Recent advances in the diagnosis and treatment of hemophagocytic lymphohistiocytosis.
@en
prefLabel
Recent advances in the diagnosis and treatment of hemophagocytic lymphohistiocytosis.
@ast
Recent advances in the diagnosis and treatment of hemophagocytic lymphohistiocytosis.
@en
P2093
P2860
P356
P1476
Recent advances in the diagnosis and treatment of hemophagocytic lymphohistiocytosis
@en
P2093
Andrea Maul-Pavicic
Gritta Janka
Kai Lehmberg
Stephan Ehl
Thomas Vraetz
Udo Zur Stadt
P2860
P2888
P356
10.1186/AR3843
P577
2012-06-08T00:00:00Z
P5875
P6179
1033988231