| scholarly article | Q13442814 |
| P356 | DOI | 10.1007/S12185-014-1591-1 |
| P698 | PubMed publication ID | 24827398 |
| P50 | author | Osamu Ohara | Q38155071 |
| P2093 | author name string | Noriko Nakajima | |
| Hiroshi Moritake | |||
| Hiroyuki Nunoi | |||
| Hideki Nakayama | |||
| Jun Okamura | |||
| Masakatsu Yanagimachi | |||
| Yasuhiro Okamoto | |||
| Yoshifumi Kawano | |||
| Jiro Inagaki | |||
| Hiroko Inada | |||
| Nobuyoshi Itonaga | |||
| Noriko Hotta | |||
| Yasufumi Hidaka | |||
| Yuichi Shinkoda | |||
| Aiko Suminoe | |||
| Sachiyo Kamimura | |||
| Maiko Shimomura | |||
| Fumio Yanai | |||
| P2860 | cites work | Nationwide survey of hemophagocytic lymphohistiocytosis in Japan. | Q51104436 |
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| A novel real-time PCR system for simultaneous detection of human viruses in clinical samples from patients with uncertain diagnoses. | Q54395819 | ||
| Successful treatment of cytomegalovirus-associated haemophagocytic syndrome following paediatric orthotopic liver transplantation | Q57080442 | ||
| Soluble interleukin-2 receptor: a useful prognostic factor for patients with hemophagocytic lymphohistiocytosis | Q70837551 | ||
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| Association of IRF5 polymorphisms with susceptibility to hemophagocytic lymphohistiocytosis in children | Q84903977 | ||
| Munc18-2 deficiency causes familial hemophagocytic lymphohistiocytosis type 5 and impairs cytotoxic granule exocytosis in patient NK cells | Q24313947 | ||
| Familial hemophagocytic lymphohistiocytosis type 5 (FHL-5) is caused by mutations in Munc18-2 and impaired binding to syntaxin 11 | Q24321783 | ||
| Macrophage activation syndrome in patients with systemic juvenile idiopathic arthritis is associated with MUNC13-4 polymorphisms | Q24654925 | ||
| Mutations of syntaxin 11 and SNAP23 genes as causes of familial hemophagocytic lymphohistiocytosis were not found in Japanese people | Q28273676 | ||
| Linkage of familial hemophagocytic lymphohistiocytosis (FHL) type-4 to chromosome 6q24 and identification of mutations in syntaxin 11 | Q28306712 | ||
| Cytomegalovirus infection-associated hemophagocytic syndrome | Q33372036 | ||
| A haemophagocytic lymphohistiocytosis (HLH)-like picture following breastmilk transmitted cytomegalovirus infection in a preterm infant | Q33374591 | ||
| HLH-2004: Diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis. | Q34561113 | ||
| Infections associated with haemophagocytic syndrome. | Q37018227 | ||
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| Familial and acquired hemophagocytic lymphohistiocytosis | Q40493224 | ||
| Cytomegalovirus-associated hemophagocytic syndrome in a patient with adult onset Still's disease. | Q40512288 | ||
| Granzyme B and perforin lytic proteins are expressed in CD34+ peripheral blood progenitor cells mobilized by chemotherapy and granulocyte colony-stimulating factor | Q41278655 | ||
| B-chronic lymphocytic leukemia cells and other B cells can produce granzyme B and gain cytotoxic potential after interleukin-21-based activation. | Q42742024 | ||
| Cytomegalovirus Retinitis During Chemotherapy With Rituximab Plus Hyperfractionated Cyclophosphamide, Vincristine, Doxorubicin, and Dexamethasone | Q42882396 | ||
| Randomized trial to compare LSA2L2-type maintenance therapy to daily 6-mercaptopurine and weekly methotrexate with vincristine and dexamethasone pulse for children with acute lymphoblastic leukemia | Q43003728 | ||
| Human B cells secrete granzyme B when recognizing viral antigens in the context of the acute phase cytokine IL-21. | Q43517682 | ||
| Cytomegalovirus retinitis as an adverse immunological effect of pulses of vincristine and dexamethasone in maintenance therapy for childhood acute lymphoblastic leukemia | Q44651799 | ||
| Histiocytosis following T-acute lymphoblastic leukemia: a BFM study. | Q46786369 | ||
| Munc13-4 is essential for cytolytic granules fusion and is mutated in a form of familial hemophagocytic lymphohistiocytosis (FHL3). | Q48219972 | ||
| Distinct mutations in STXBP2 are associated with variable clinical presentations in patients with familial hemophagocytic lymphohistiocytosis type 5 (FHL5). | Q50431126 | ||
| P433 | issue | 1 | |
| P921 | main subject | lymphoblastic leukemia | Q18553852 |
| hemophagocytic lymphohistiocytosis | Q1642170 | ||
| P304 | page(s) | 70-78 | |
| P577 | publication date | 2014-05-15 | |
| P1433 | published in | International Journal of Hematology | Q6051416 |
| P1476 | title | Clinical characteristics and genetic analysis of childhood acute lymphoblastic leukemia with hemophagocytic lymphohistiocytosis: a Japanese retrospective study by the Kyushu-Yamaguchi Children's Cancer Study Group | |
| P478 | volume | 100 |
| Q38473148 | A review of blood diseases and cytopenias associated with human parvovirus B19 infection |
| Q41709035 | A systematic review of malignancy-associated hemophagocytic lymphohistiocytosis that needs more attentions |
| Q26798093 | B-acute lymphoblastic leukemia/lymphoblastic lymphoma |
| Q42015092 | Hemophagocytosis by Leukemic Blasts in T Cell Acute Lymphoblastic Leukemia: An Unusual Finding |
| Q36833380 | Periconceptional folate consumption is associated with neonatal DNA methylation modifications in neural crest regulatory and cancer development genes |
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