听力与言语-语言病理学

行为科学

医学伦理学

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  • Continuous complete hematological and cytogenetic remission with molecular minimal residual disease 9 years after discontinuation of interferon-alpha in a patient with Philadelphia chromosome-positive chronic myeloid leukemia.

    abstract::Interferon-alpha has been used as standard therapy for patients with Philadelphia-positive chronic myeloid leukemia (CML) for more than 20 years. Recently randomized trials have shown a superiority of the tyrosine kinase inhibitor imatinib in respect to its efficacy to induce complete hematological and cytogenetic rem...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000089476

    authors: Verbeek W,König H,Boehm J,Kohl D,Lange C,Heuer T,Scheibenbogen C,Reis HE,Hochhaus A,Graeven U

    更新日期:2006-01-01 00:00:00

  • Bortezomib-induced rhabdomyolysis in multiple myeloma.

    abstract::Although multiple myeloma (MM) remains an incurable disease, its treatment has improved over the past decade. This improvement has been at least in part due to the introduction of novel antimyeloma agents with new mechanisms of action, including those that target both myeloma cells and the tumor microenvironment, with...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000094682

    authors: Cibeira MT,Mercadal S,Arenillas L,Muntañola A,Salamero O,Bladé J

    更新日期:2006-01-01 00:00:00

  • CD56-positive acute lymphoblastic leukemia.

    abstract::We report a patient with lung cancer who developed CD56-positive acute lymphoblastic leukemia. He was referred to our hospital for thrombocytopenia. Atypical cells were found in the blood and the bone marrow. These cells were immunophenotypically positive for CD3epsilon, CD56, and terminal deoxynucleotidyl transferase...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000087891

    authors: Matano S,Terahata S,Nakamura S,Kobayashi K,Sugimoto T

    更新日期:2005-01-01 00:00:00

  • Maternal, neonatal and collection factors influencing the haematopoietic content of cord blood units.

    abstract:BACKGROUND AND OBJECTIVES:Umbilical cord blood (UCB) contains haematopoietic stem cells and can be used as an alternative to bone marrow transplantation in certain cases. Engraftment was dependent upon the haematopoietic progenitor cell content of the cord blood units. This study was designed to investigate the influen...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000084677

    authors: Solves P,Perales A,Moraga R,Saucedo E,Soler MA,Monleon J

    更新日期:2005-01-01 00:00:00

  • A case of pure red cell aplasia complicated with diffuse large B cell lymphoma, T-cell-rich/histiocyte-rich variant: effectiveness of rituximab and implications for a common immunopathogenic role of B lymphocytes.

    abstract::Diffuse large B cell lymphoma, T-cell-rich/histiocyte-rich variant (DLBL-TH), is characterized by the presence of neoplastic B cells set in a background containing numerous non-neoplastic T lymphocytes and histiocytes. We report here the case of a patient with DLBL-TH who developed overt pure red cell aplasia (PRCA) f...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000084450

    authors: Oyaizu N,Kozai Y,Kodo H,Sunaga S,Iwabuchi K,Higashihara M,Mori S

    更新日期:2005-01-01 00:00:00

  • Future directions in haematology: beyond multiple myeloma.

    abstract::Thalidomide acts on the microenvironment of myelodysplastic syndromes (MDS) by influencing cytokine networks, and growing evidence supports thalidomide's usefulness in the management of haematological malignancies, such as MDS. The European Collaboration Group on Myelofibrosis with Myeloid Metaplasia reviewed patients...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000087042

    authors: Prentice HG,Sacchi S,Russell N

    更新日期:2005-01-01 00:00:00

  • Comparative measurement of anti-factor VIII antibody by Bethesda assay and ELISA reveals restricted isotype profile and epitope specificity.

    abstract::Factor VIII (FVIII) inhibitor antibodies are produced against functional epitopes of FVIII in about 30% of severe hemophilia A patients leading to inhibition of its procoagulant activity. The Bethesda assay, the most commonly used method to measure FVIII inhibitors, based on inhibition of coagulant activity of FVIII, ...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000086580

    authors: Towfighi F,Gharagozlou S,Sharifian RA,Kazemnejad A,Esmailzadeh K,Managhchi MR,Shokri F

    更新日期:2005-01-01 00:00:00

  • The significance of minimal residual disease in stem cell grafts and the role of purging: is it better to purge in vivo or in vitro?

    abstract::Contamination of autologous graft by tumor, in addition to incomplete tumor eradication, can partly explain why relapse remains the commonest cause of treatment failure after autologous stem cell transplantation (ASCT) in patients with malignant hematologic disorders. Monitoring of minimal residual disease (MRD) is no...

    journal_title:Acta haematologica

    pub_type: 杂志文章,评审

    doi:10.1159/000088411

    authors: Melillo L,Cascavilla N,Lerma E,Corsetti MT,Carella AM

    更新日期:2005-01-01 00:00:00

  • Absence of gene mutation in TRAIL receptor 1 (TRAIL-R1) and TRAIL receptor 2 (TRAIL-R2) in chronic myelogenous leukemia and myelodysplastic syndrome, and analysis of mRNA Expressions of TRAIL and TRAIL-related genes in chronic myelogenous leukemia.

    abstract::Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) is an interferon (IFN)-induced molecule with apoptotic activity. We examined gene mutations in the death domains of TRAIL receptor 1 (TRAIL-R1) and TRAIL receptor 2 (TRAIL-R2), and in the TRAIL gene promoter in 46 chronic myelogenous leukemia (CML) patien...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000083449

    authors: Liu LG,Tanaka H,Ito K,Ito T,Sultana TA,Kyo T,Kimura A

    更新日期:2005-01-01 00:00:00

  • Strategies and clinical implications of chimerism diagnostics after allogeneic hematopoietic stem cell transplantation.

    abstract::Analysis of donor chimerism has become a routine method for the documentation of engraftment after allogeneic hematopoietic stem cell transplantation (HSCT). In recent years several groups have also focused on the application of this technique for the detection of relapsing disease after allogeneic HSCT. This review a...

    journal_title:Acta haematologica

    pub_type: 杂志文章,评审

    doi:10.1159/000077555

    authors: Thiede C,Bornhäuser M,Ehninger G

    更新日期:2004-01-01 00:00:00

  • Molecular and clinical follow-up after treatment of multiple myeloma.

    abstract::Multiple myeloma (MM) is a B cell malignancy characterized by accumulation of plasma cells (PCs) in the bone marrow. Traditional methods for the detection of minimal residual disease (MRD) measure the presence of monoclonal immunoglobulin protein secreted by the malignant PCs. However, changes in the level of MRD in M...

    journal_title:Acta haematologica

    pub_type: 杂志文章,评审

    doi:10.1159/000077565

    authors: Rasmussen T,Knudsen LM,Huynh TK,Johnsen HE

    更新日期:2004-01-01 00:00:00

  • T cell prolymphocytic leukemia with new chromosome rearrangements.

    abstract::A 77-year-old woman presented to the outpatient hematology clinic in August 2001 with leukocytosis, recurrent bacterial infections, sweating and weight loss. Bone marrow biopsy showed 80% infiltration with lymphoid cells having a prolymphocytic morphology. Flow-cytometric immunophenotype analysis showed that over 80% ...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000076527

    authors: Zver S,Kokalj Vokac N,Zagradisnik B,Erjavec A,Zagorac A,Zupan IP,Cernelc P

    更新日期:2004-01-01 00:00:00

  • Eosinophilic gastroenteritis or eosinophilic chloroma?

    abstract::Granulocytic sarcoma of the small intestine preceding or as the presenting feature of acute myelogenous leukemia with chromosome 16 abnormalities has been observed in at least 4 patients. We report the case of a patient initially diagnosed with eosinophilic gastroenteritis, responding to corticosteroid treatment for 2...

    journal_title:Acta haematologica

    pub_type: 杂志文章,评审

    doi:10.1159/000079729

    authors: Julia A,Nomdedeu JF

    更新日期:2004-01-01 00:00:00

  • Treatment of beta-thalassemia patients with recombinant human erythropoietin: effect on transfusion requirements and soluble adhesion molecules.

    abstract::The most common single genetic disorder and a major public health issue in Greece and other Mediterranean countries is beta-thalassemia. Current therapeutic approaches for homozygous beta-thalassemia entail blood transfusions and iron chelation therapy with deferoxamine or deferiprone for preventing tissue hemosideros...

    journal_title:Acta haematologica

    pub_type: 临床试验,杂志文章

    doi:10.1159/000077551

    authors: Chaidos A,Makis A,Hatzimichael E,Tsiara S,Gouva M,Tzouvara E,Bourantas KL

    更新日期:2004-01-01 00:00:00

  • Mediastinal bulky tumour in Hodgkin's disease and prognostic value of positron emission tomography in the evaluation of post-treatment residual masses.

    abstract::Among the 193 patients (82 female, 111 male) treated primarily for Hodgkin's disease at our clinic between 1990 and 2001 and followed up until 2003, 42 (22%) had mediastinal bulky tumours (MBTs) by the Cotswolds criteria. The rate of MBT diagnosis was significantly greater in the early stage of the disease, these pati...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000081271

    authors: Keresztes K,Lengyel Z,Devenyi K,Vadasz G,Miltenyi Z,Illes A

    更新日期:2004-01-01 00:00:00

  • Gene therapy targeting hematopoietic cells: better not leave it to chance.

    abstract::Gene therapy targeting hematopoietic cells has arrived at a new stage of potency. While the potential for curing inherited disorders of the immune system has been demonstrated in clinical trials, we were also confronted with the first serious adverse events related to random insertion of foreign DNA into cellular chro...

    journal_title:Acta haematologica

    pub_type: 杂志文章,评审

    doi:10.1159/000072459

    authors: Baum C,von Kalle C

    更新日期:2003-01-01 00:00:00

  • Cytokine gene expression in regenerating haematopoietic tissues of mice after cyclophosphamide treatment.

    abstract::The goal of the study was to investigate changes in expression of selected growth factors tentatively involved in regeneration of haematopoietic tissues (bone marrow and spleen) following cyclophosphamide (CY) damage in the mouse. The bone marrow (BM) and spleen were examined separately, since the regenerating pattern...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000068490

    authors: Psenák O,Sefc L,Sýkora V,Chang KT,Necas E

    更新日期:2003-01-01 00:00:00

  • Apoptosis in relation to CD34 antigen expression in normal and myelodysplastic bone marrow.

    abstract::An increased bone marrow (BM) apoptosis is one of the mechanisms responsible for the ineffective hematopoiesis of myelodysplastic syndromes (MDS). It is controversial whether the excessive apoptosis in myelodysplasia predominantly involves the subset of progenitor cells or of maturing cells. We investigated the degree...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000067275

    authors: Pecci A,Travaglino E,Klersy C,Invernizzi R

    更新日期:2003-01-01 00:00:00

  • Avascular necrosis of the femoral head in adult Kuwaiti sickle cell disease patients.

    abstract::While sickle cell disease (SCD) is generally mild in most Kuwaitis, because of their elevated fetal Hb levels, avascular necrosis of the femoral head (AVNFH) appears to be a common complication. It was recently documented in 26.7% of Kuwaiti children with SCD. There have, however, been no previous studies of adult pat...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000072406

    authors: Marouf R,Gupta R,Haider MZ,Al-Wazzan H,Adekile AD

    更新日期:2003-01-01 00:00:00

  • Utility of a prognostic scoring system for allogeneic stem cell transplantation in patients with chronic myeloid leukemia.

    abstract::Allogeneic stem cell transplantation (SCT) is the treatment of choice for selected patients with chronic myeloid leukemia (CML). However, it is associated with a high risk of treatment-related mortality (TRM) and morbidity. To assist in decision making about transplantation, a simple scoring system to assess the risk ...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000069283

    authors: Qazilbash MH,Devetten MP,Abraham J,Lynch JP,Beall CL,Weisenborn R,Bunner P,Ericson SG

    更新日期:2003-01-01 00:00:00

  • Intermediate-dose cyclophosphamide and granulocyte colony-stimulating factor is a valid alternative to high-dose cyclophosphamide for mobilizing peripheral blood CD34+ cells in patients with multiple myeloma.

    abstract::Peripheral blood stem cells (PBSC) are widely used in the setting of dose-intensive chemotherapies in patients with multiple myeloma (MM). Although the granulocyte colony-stimulating factor (G-CSF), following chemotherapy or not, is considered the standard growth factor for mobilizing PBSC, the optimal chemotherapeuti...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000070967

    authors: Petrucci MT,Avvisati G,La Verde G,De Fabritiis P,Ribersani M,Palumbo G,De Felice L,Rusignuolo A,Simone F,Meloni G,Mandelli F

    更新日期:2003-01-01 00:00:00

  • High-dose therapy and autologous stem cell transplantation in relapsed and refractory Hodgkin's disease: outcome based on a prognostic model.

    abstract::We evaluated the results of high-dose therapy (HDT) and autologous hematopoietic stem cell transplantation (ASCT) in patients with relapsed or primary refractory Hodgkin's disease (HD), using a previously reported prognostic model based on the presence of three poor prognostic factors at the start of salvage therapy/p...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000074220

    authors: Qazilbash MH,Devetten MP,Abraham J,Lynch JP,Beall CL,Auber M,Weisenborn R,Bunner P,Ericson SG

    更新日期:2003-01-01 00:00:00

  • Chronic haemolytic anaemia and glucose-6 phosphate dehydrogenase deficiency. Case report and review of the literature.

    abstract::Deficiency in glucose-6-phosphate dehydrogenase (G6PD) is the most common enzymopathy, and more than 125 different mutations causing G6PD deficiency have been identified. Chronic haemolytic anaemia (CHA) associated with G6PD deficiency is rare, but there is a cluster of mutations causing CHA between amino acids 361-42...

    journal_title:Acta haematologica

    pub_type: 杂志文章,评审

    doi:10.1159/000064749

    authors: Hundsdoerfer P,Vetter B,Kulozik AE

    更新日期:2002-01-01 00:00:00

  • Roles of hematopoietic transcription factors GATA-1 and GATA-2 in the development of red blood cell lineage.

    abstract::The transcription factors GATA-1 and GATA-2 play key roles in gene regulation during erythropoiesis. Gene ablation studies in mouse revealed that GATA-2 is crucial for the maintenance and proliferation of immature hematopoietic progenitors, whereas GATA-1 is essential for the survival of erythroid progenitors as well ...

    journal_title:Acta haematologica

    pub_type: 杂志文章,评审

    doi:10.1159/000065660

    authors: Ohneda K,Yamamoto M

    更新日期:2002-01-01 00:00:00

  • Remission induction of refractory anaemia with excess blasts in transformation by sole treatment with granulocyte colony-stimulating factor with persistent chromosomal abnormality.

    abstract::We report a patient with myelodysplastic syndrome (MDS), refractory anaemia with excess blasts in transformation, in whom complete remission (CR) was achieved with the administration of granulocyte colony-stimulating factor (G-CSF). The 76-year-old patient was admitted to our hospital with a fever and a productive cou...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000057637

    authors: Kondo H,Kasahara Y,Mori A

    更新日期:2002-01-01 00:00:00

  • A fourth case of 8p11 myeloproliferative disorder transforming to B-lineage acute lymphoblastic leukaemia. A case report.

    abstract::A 56-year-old male presented with inguinal lymphadenopathy and leucocytosis (WBC 98 x 10(9)/l). Bone marrow morphology showed myeloid hyperplasia, with eosinophilia. Cytogenetic analysis showed no evidence of the Philadelphia chromosome, and fluorescence in situ hybridisation studies for the BCR/ABL fusion were negati...

    journal_title:Acta haematologica

    pub_type: 杂志文章,评审

    doi:10.1159/000046638

    authors: JabbarAl-Obaidi M,Rymes N,White P,Pomfret M,Smith H,Starczynski J,Johnson R

    更新日期:2002-01-01 00:00:00

  • Bacteria in blood smears: overwhelming sepsis or trivial contamination.

    abstract::It is unusual to find microorganisms in peripheral blood smears, and their presence is frequently associated with overwhelming sepsis and consequently a poor prognosis. In this report, we demonstrate 4 cases with bacteria in blood smears. Two of them had a fatal outcome, but the other 2 were caused by a contamination ...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000058318

    authors: van der Meer W,Verwiel JM,Gidding CE,de Metz M,de Keijzer MH

    更新日期:2002-01-01 00:00:00

  • Mesenteric panniculitis presenting with autoimmune haemolytic anaemia.

    abstract::Mesenteric panniculitis is a rare idiopathic inflammatory disorder that can lead to sclerosis. We describe a patient with mesenteric panniculitis presenting with abdominal symptoms and autoimmune haemolytic anaemia. The symptoms remitted after splenectomy and gradual steroid taper. This may suggest an autoimmune compo...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000046627

    authors: Vidarsson B,Matthíasson P,Agnarsson BA,Onundarson PT

    更新日期:2002-01-01 00:00:00

  • Routine screening of (--(SEA)) alpha-thalassemia deletion by an enzyme-linked immunosorbent assay for embryonic zeta-globin chains.

    abstract::We evaluated an enzyme-linked immunosorbent assay (ELISA) for embryonic zeta-globin chains as a routine screening test for (--(SEA)) alpha-thalassemia deletion (SEA deletion). A total of 174 consecutive patient samples with a request for Hb analysis were recruited. The ELISA method was evaluated against a polymerase c...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000063060

    authors: Ma SK,Ma V,Chan AY,Chan LC,Chui DH

    更新日期:2002-01-01 00:00:00

  • Avascular necrosis of the hip in children with sickle cell disease and high Hb F: magnetic resonance imaging findings and influence of alpha-thalassemia trait.

    abstract::Avascular necrosis (AVN) of the hip is a common cause of morbidity in sickle cell disease (SCD). Its prevalence increases with age and predisposing factors include coexistent alpha-thalassemia trait, frequent vaso-occlusive crisis and a high hematocrit (Hct). SCD is relatively mild among Kuwaiti patients because of th...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000046529

    authors: Adekile AD,Gupta R,Yacoub F,Sinan T,Al-Bloushi M,Haider MZ

    更新日期:2001-01-01 00:00:00

  • Mesenchymal differentiation and organ distribution of established human stromal cell lines in NOD/SCID mice.

    abstract::Two human stromal cell lines were established previously from bone marrow-derived primary long-term cultures by immortalization using the SV40 large T antigen and cellular cloning. After irradiation, the fibroblast-like cell lines L87/4 and L88/5 support hematopoietic differentiation of allogeneic cord blood cells in ...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000046559

    authors: Thalmeier K,Meissner P,Moosmann S,Sagebiel S,Wiest I,Huss R

    更新日期:2001-01-01 00:00:00

  • Monocytoid B cell lymphoma associated with antibodies to myelin-associated glycoprotein and sulphated glucuronyl paragloboside.

    abstract::Monocytoid B cell lymphoma (MBCL) is an immunologically and morphologically well-defined low-grade lymphoma with a predilection for lymph nodes of the parotid region. We describe an association of MBCL with anti-myelin-associated glycoprotein (MAG) polyneuropathy in a 53-year-old male. The diagnosis of stage IV MBCL w...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000046603

    authors: Donfrid M,Apostolski S,Suvajdzić N,Janković G,Cemerikić-Martinović V,Atkinson HD,Colovic M

    更新日期:2001-01-01 00:00:00

  • Increased proportion of HLA-class-I-specific natural killer cell receptors (CD94) on peripheral blood mononuclear cells after allogeneic bone marrow transplantation.

    abstract::In the present study, we investigated the inhibitory natural killer cell receptor (NKR) expression of CD94/NKG2A on PBMC after allogeneic bone marrow transplantation (BMT). The proportion of CD94 expression on PBMC was higher in patients without chronic graft-versus-host disease (cGVHD) and also in cGVHD patients with...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000046540

    authors: Tanaka J,Tutumi Y,Zhang L,Mori A,Kahata K,Toyoshima N,Ohta S,Kobayashi S,Hashino S,Asaka M,Imamura M

    更新日期:2001-01-01 00:00:00

  • Thromboprophylaxis in the cancer patient.

    abstract::Cancer patients not undergoing treatment and without a history of venous thrombosis do not, as a general rule, require prophylaxis. However, venous thromboembolism is of sufficient magnitude in patients undergoing treatment for cancer for thromboprophylaxis to be routinely employed. The mainstay of primary prevention ...

    journal_title:Acta haematologica

    pub_type: 杂志文章,评审

    doi:10.1159/000046592

    authors: Thodiyil PA,Walsh DC,Kakkar AK

    更新日期:2001-01-01 00:00:00

  • Gene rearrangements in bone marrow cells of patients with acute myelogenous leukemia.

    abstract::At diagnosis, clonal gene rearrangement probes [retinoic acid receptor (RAR)-alpha, major breakpoint cluster region (M-bcr), immunoglobulin (Ig)-JH, T cell receptor (TcR)-beta, myeloid lymphoid leukemia (MLL) or cytokine genes (GM-CSF, G-CSF, IL-3)] were detected in bone marrow samples from 71 of 153 patients with acu...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000041035

    authors: Schmetzer HM,Braun S,Wiesner D,Duell T,Gerhartz HH,Mittermueller J

    更新日期:2000-01-01 00:00:00

  • Are haemochromatosis mutations related to the severity of liver disease in hepatitis C virus infection?

    abstract::It has been proposed that iron overload may adversely affect liver disease outcome. The recent identification of 2 mutations in the HFE gene related to hereditary haemochromatosis (Cys282Tyr and His63Asp) provided an opportunity to test whether they are associated with hepatic iron accumulation and the activity and se...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000040991

    authors: Martinelli AL,Franco RF,Villanova MG,Figueiredo JF,Secaf M,Tavella MH,Ramalho LN,Zucoloto S,Zago MA

    更新日期:2000-01-01 00:00:00

  • Predictive factors for cure after immunosuppressive therapy of aplastic anemia.

    abstract::In a previous study, we evaluated efficacy of repeated antilymphocyte globulin (ALG) treatment for patients with severe aplastic anemia not responding to an initial ALG treatment or relapsing after initial response to ALG. We now searched in the same cohort of patients for differences between patients who responded to...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000041005

    authors: Viollier R,Tichelli A

    更新日期:2000-01-01 00:00:00

  • Influence of alpha-thalassemia trait on the prevalence and severity of anemia in pregnancy among women in Kuwait.

    abstract::Alpha-thalassemia is very common in the Kuwaiti population, but its influence on anemia of pregnancy has not been previously investigated. We have screened a group of 59 anemic (Hb < 11 g/dl) pregnant women for the alpha-thal-2 (-alpha-3.7 kb) deletion which is the commonest alpha-thal allele in this community, using ...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000039757

    authors: Diejomaoh FM,Haider MZ,Dalal H,Abdulaziz A,D'Souza TM,Adekile AD

    更新日期:2000-01-01 00:00:00

  • Littoral cell angioma associated with portal hypertension and resected colon cancer.

    abstract::Littoral cell angioma (LCA) is a rare vascular tumor of the spleen with an unknown etiology and unclear natural history. An association with synchronous malignancy has been described. We report the case of a 54-year-old woman who had progressive splenomegaly over 3 years following resection of a colon adenocarcinoma. ...

    journal_title:Acta haematologica

    pub_type: 杂志文章,评审

    doi:10.1159/000039747

    authors: Steensma DP,Morice WG

    更新日期:2000-01-01 00:00:00

  • Granulocytic sarcoma with breast and skin presentation: a report of a case successfully treated by local radiation and systemic chemotherapy.

    abstract::Granulocytic sarcoma (GS) is a rare extramedullary tumor composed of immature myeloid cells. It is usually associated with leukemia or other myeloproliferative disorders, but can also occur without overt hematologic disease, i.e. in patients with a normal bone marrow and no history of acute myelogenous leukemia. This ...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000041067

    authors: Breccia M,Petti MC,Fraternali-Orcioni G,Monarca B,Latagliata R,D'Elia GM,Mandelli F,Pileri SA

    更新日期:2000-01-01 00:00:00

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