- Attempts to treat patients with hemophilia, the "royal disease"
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Park R
- KMID: 2172866
- Blood Res.
- 2013 Dec;48(4):235-236.
- doi: 10.5045/br.2013.48.4.235
No abstract available. -
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- A new paradigm in the diagnosis of hereditary hemolytic anemia
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Jung HL
- KMID: 2172867
- Blood Res.
- 2013 Dec;48(4):237-239.
- doi: 10.5045/br.2013.48.4.237
No abstract available. -
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- Late but effective long-term response to splenectomy in the treatment of immune thrombocytopenia
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Scaramucci L, Giovannini M, Tendas A, Niscola P, de Fabritiis P
- KMID: 2172881
- Blood Res.
- 2013 Dec;48(4):297-298.
- doi: 10.5045/br.2013.48.4.297
No abstract available. -
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- Acute promyelocytic leukemia with an unusual presentation of secondary postpartum hemorrhage
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Sharma S, Pujani M, Tejwani N
- KMID: 2172882
- Blood Res.
- 2013 Dec;48(4):299-300.
- doi: 10.5045/br.2013.48.4.299
No abstract available. -
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- Relapsed intravascular large B-cell lymphoma
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Jo KI, Park R, Won JH
- KMID: 2172868
- Blood Res.
- 2013 Dec;48(4):240-240.
- doi: 10.5045/br.2013.48.4.240
No abstract available. -
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- Primary mixed-type autoimmune hemolytic anemia concomitant with acute splanchnic venous thrombosis of idiopathic origin in a young woman: an unexplained association
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Scaramucci L, Giovannini M, Niscola P, Perrotti A, de Fabritiis P
- KMID: 2172878
- Blood Res.
- 2013 Dec;48(4):292-293.
- doi: 10.5045/br.2013.48.4.292
No abstract available. -
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- Lymphoplasmacytic non-Hodgkin lymphoma/Waldenstrom's macroglobulinemia with CD5+, CD23+, and CD10-
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D'Angelo G, Hotz AM, Monti M
- KMID: 2172883
- Blood Res.
- 2013 Dec;48(4):300-303.
- doi: 10.5045/br.2013.48.4.300
No abstract available. -
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- Chronic myeloid leukemia with marked splenomegaly and pseudo-Gaucher cells
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Yang HS, Cho KS, Park TS
- KMID: 2172869
- Blood Res.
- 2013 Dec;48(4):241-241.
- doi: 10.5045/br.2013.48.4.241
No abstract available. -
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- Primary diffuse large B-cell lymphoma of the bone marrow in a frail and elderly patient successfully treated with rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone
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Niscola P, Palombi M, Fratoni S, Perrotti A, de Fabritiis P
- KMID: 2172880
- Blood Res.
- 2013 Dec;48(4):296-297.
- doi: 10.5045/br.2013.48.4.296
No abstract available. -
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- Successful treatment of steroid resistant hypereosinophilic syndrome with low-dose CsA
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Jung YH, Han SB, Park YJ, Woo IS, Cho BK, Han CW
- KMID: 2172879
- Blood Res.
- 2013 Dec;48(4):293-295.
- doi: 10.5045/br.2013.48.4.293
No abstract available. -
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- Comparison of laboratory characteristics between acute promyelocytic leukemia and other subtypes of acute myeloid leukemia with disseminated intravascular coagulation
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Lee HJ, Park HJ, Kim HW, Park SG
- KMID: 2172871
- Blood Res.
- 2013 Dec;48(4):250-253.
- doi: 10.5045/br.2013.48.4.250
BACKGROUND: Acute promyelocytic leukemia (APL) is an acute myeloid leukemia (AML) subtype with distinctive cell morphology, molecular presentation, clinical course, and treatment. About 90% of APL patients present with hemorrhagic... -
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- Sequential therapy with activated prothrombin complex concentrates and recombinant activated factor VII to treat unresponsive bleeding in patients with hemophilia and inhibitors: a single center experience
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Han MH, Park YS
- KMID: 2172876
- Blood Res.
- 2013 Dec;48(4):282-286.
- doi: 10.5045/br.2013.48.4.282
BACKGROUND: Currently, the greatest challenge in hemophilia treatment is managing hemophilia patients with inhibitors. The two main bypassing agents that are used to treat hemophilia patients with inhibitors are activated... -
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- Nodular lymphoid hyperplasia of the stomach in a patient with multiple submucosal tumors
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Jeon JY, Lim SG, Kim JH, Lee KM, Cho SR, Han JH
- KMID: 2172877
- Blood Res.
- 2013 Dec;48(4):287-291.
- doi: 10.5045/br.2013.48.4.287
Nodular lymphoid hyperplasia of the stomach is a rare lymphoproliferative disorder. Here, we report a 38-year-old man who presented with multiple submucosal tumors of the stomach. Histologically, the lesions were... -
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- Next generation sequencing: new tools in immunology and hematology
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Mori A, Deola S, Xumerle L, Mijatovic , Malerba G, Monsurro V
- KMID: 2172870
- Blood Res.
- 2013 Dec;48(4):242-249.
- doi: 10.5045/br.2013.48.4.242
One of the hallmarks of the adaptive immune system is the specificity of B and T cell receptors. Thanks to somatic recombination, a large repertoire of receptors can be generated... -
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- Sequential chemotherapy followed by radiotherapy versus concurrent chemoradiotherapy in patients with stage I/II extranodal natural killer/T-cell lymphoma, nasal type
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Lee J, Kim CY, Park YJ, Lee NK
- KMID: 2172875
- Blood Res.
- 2013 Dec;48(4):274-281.
- doi: 10.5045/br.2013.48.4.274
BACKGROUND: The purpose of this report is to summarize our clinical experience of patients with stage I/II extranodal natural killer (NK)/T-cell lymphoma, nasal type, treated using sequential chemotherapy followed by... -
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- Posterior reversible encephalopathy syndrome in pediatric patients undergoing treatment for hemophagocytic lymphohistiocytosis: clinical outcomes and putative risk factors
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Lee G, Lee SE, Ryu KH, Yoo ES
- KMID: 2172873
- Blood Res.
- 2013 Dec;48(4):258-265.
- doi: 10.5045/br.2013.48.4.258
BACKGROUND: Hemophagocytic lymphohistiocytosis (HLH) is a rare multiorgan disease of toxic immune activation caused by the interaction of cytotoxic T cells and innate immune cells and frequently involves the central... -
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- Prognostic value of immunohistochemical algorithms in gastrointestinal diffuse large B-cell lymphoma
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Hwang HS, Yoon DH, Suh C, Park CS, Huh J
- KMID: 2172874
- Blood Res.
- 2013 Dec;48(4):266-273.
- doi: 10.5045/br.2013.48.4.266
BACKGROUND: Diffuse large B-cell lymphoma (DLBCL) is a heterogeneous clinicopathological entity, and its molecular classification into germinal center B cell-like (GCB) and activated B cell-like (ABC) subtypes using gene expression... -
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- Clinical characteristics of hemophagocytic lymphohistiocytosis following Kawasaki disease: differentiation from recurrent Kawasaki disease
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Kang HR, Kwon YH, Yoo ES, Ryu KH, Kim JY, Kim HS, Kim HM, Lee YH
- KMID: 2172872
- Blood Res.
- 2013 Dec;48(4):254-257.
- doi: 10.5045/br.2013.48.4.254
BACKGROUND: Our aim was to investigate the clinical pattern of hemophagocytic lymphohistiocytosis following Kawasaki disease (HLH-KD), to enable differentiation of HLH from recurrent or refractory KD and facilitate early diagnosis. METHODS:... -
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