Identification of Hb Q-India (alpha64 Asp-->His) in Thailand.

Abstract:

:More than 30 different hemoglobin variants either affecting alpha or beta globin chains have been identified in Thailand. The large variety in the different forms of hemoglobinopathy contributes to several complicated interactions, since different types of defective globin alleles are prevalent in Thailand and nearly 30-40% of the population are carriers of either alpha or beta thalassemia (thal). Many rare and novel abnormal globin variants in Thai subjects have been identified in our laboratory within the past few years; including Hb Lepore-Hollandia, homozygous Hb Tak, Hb Dhonburi, Hb G-Makassar, Hb G-Coushatta, Hb New York, Hb Paksè and Hb Pak Num Po. In addition to these, here we report, for the first time, the identification of Hb Q-India, an innocuous alpha globin variant, in a Thai family with Indian ancestry. This report highlights the complexity associated with identifying unknown globin variants within a population that has a heterogeneous repertoire of globin chain disorders.

journal_name

Hematology

authors

Viprakasit V,Chinchang W,Pung-Amritt P,Tanphaichitr VS

doi

10.1080/10245330310001652455

subject

Has Abstract

pub_date

2004-04-01 00:00:00

pages

151-5

issue

2

eissn

1024-5332

issn

1607-8454

pii

6QLFGLDMELTCN5AD

journal_volume

9

pub_type

杂志文章

相关文献

文献大全
  • Erythropoiesis: Short Report: Translation of Analysis Results between Serum Ferritin Assays, Ferritin RIA AmershamTM and Abbott AxSYMTM Ferritin.

    abstract::The serum ferritin assays, Ferritin RIA Amersham(TM) and Abbott AxSYM(TM) Ferritin were compared in order to translate values from one assay to the other. Serum ferritin was analysed with both assays in 102 samples. Logarithmic transformation of the results was performed in order to stabilize the variance. The relatio...

    journal_title:Hematology (Amsterdam, Netherlands)

    pub_type: 杂志文章

    doi:

    authors: Milman N,Byg KE,Juul-Jørgensen B,Weis Bentzon M

    更新日期:1999-01-01 00:00:00

  • Malignancy: X-Linked Cytochrome B Positive Chronic Granulomatous Disease treated by Bone Marrow Transplantation.

    abstract::Chronic granulomatous disease is caused by a genetic defect in the oxidase of phagocytic cells which results in increased susceptibility to recurrent infections. Conventional treatment includes the use of antimicrobials and interpheron-gamma. This study was performed to assess the clinical efficacy of allogeneic bone ...

    journal_title:Hematology (Amsterdam, Netherlands)

    pub_type: 杂志文章

    doi:10.1080/10245332.1999.11746454

    authors: Di Bartolomeo P,Papalinetti G,Olioso P,Di Girolamo G,Bavaro P,De Mattia D,Manzionna MM,Schettini F,Torlontano G

    更新日期:1999-01-01 00:00:00

  • Malignancy: 2'-Chlorodeoxyadenosine Effectively Induces Complete Remission in Hairy Cell Leukaemia.

    abstract::Hairy cell leukaemia, previously known as leukaemic reticuloendotheliosis, is an indolent lymphoproliferative disorder of unknown etiology. It typically affects males, causes marked splenomegaly and moderate enlargement of the liver, whilst lymphadenopathy is inconspicuous. Pancytopenia is characteristic with unusuall...

    journal_title:Hematology (Amsterdam, Netherlands)

    pub_type: 杂志文章

    doi:

    authors: Jacobs P,Wood L,Mansvelt EP,Gartrell K

    更新日期:2000-01-01 00:00:00

  • Malignancy: Case report: Myelodysplasia Following Treatment of Chronic Lymphocytic Leukaemia with Fludarabine.

    abstract::Recently there has been an increased awareness of a possible link between the use of purine nucleoside analogues and myelodysplasia. We report the case of a patient who developed myelodysplasia with complex cytogenetic changes after receiving fludarabine. We review the literature, discuss the possible links between my...

    journal_title:Hematology (Amsterdam, Netherlands)

    pub_type: 杂志文章

    doi:

    authors: Hennessy BJ,Ryley S,Kasprzyk A,Reid CD

    更新日期:2000-01-01 00:00:00

  • BMT: Bone Marrow Transplant Associated Thrombotic Microangiopathy.

    abstract::Thrombotic microangiopathy is a severe microvascular disorder which may occur in up to 70% of patients undergoing bone marrow transplant. Clinically the term thrombotic microangiopathy encompasses a wide spectrum of syndromes, most importantly the thrombotic thrombocytopenic purpura (TTP) and hemolytic uremic syndrome...

    journal_title:Hematology (Amsterdam, Netherlands)

    pub_type: 杂志文章

    doi:10.1080/10245332.2000.11746488

    authors: Busca A,Uderzo C

    更新日期:2000-01-01 00:00:00

  • Therapy: Hyperbaric Oxygen as the Only Effective Treatment in Mutilating and Resistant Systemic Vasculitis.

    abstract::A forty year old man was seen in 1984 with a four year history of a painful vasculitis that responded transiently to plasma exchange. Diagnosis was revised to atypical pyoderma gangrenosum with further temporary benefit from lamprene and continuing maximally tolerated corticosteroids. The course fluctuated over the ne...

    journal_title:Hematology (Amsterdam, Netherlands)

    pub_type: 杂志文章

    doi:10.1080/10245332.2000.11746504

    authors: Jacobs P,Wood L,Van Niekerk GD

    更新日期:2000-01-01 00:00:00

  • Pentoxifylline, Ciprofloxacin and Dexamethasone Improve the Ineffective Hematopoiesis in Myelodysplastic Syndrome Patients; Malignancy.

    abstract::Twenty-five patients with a diagnosis of myelodysplastic syndromes (MDS) were randomized to either begin therapy with pentoxifylline, ciprofloxacin and dexamethasone (PCD) immediately (10 patients) or after a 12 week observation period (control arm, 15 patients). PCD was administered with the goal of suppressing cytok...

    journal_title:Hematology (Amsterdam, Netherlands)

    pub_type: 杂志文章

    doi:10.1080/10245332.2000.11746517

    authors: Raza A,Qawi H,Andric T,Dar S,Lisak L,Huang RW,Venugopal P,Gezer S,Gregory SA,Hsu WT,Loew J,Robin E,Rifkin S,Shah R,Divgi A,Taylor R,Grosset A

    更新日期:2000-01-01 00:00:00

  • Cephalosporin-induced Hemolytic Anemia in a Sicilian Child; Erythropoiesis.

    abstract::A 27-month-old child developed acute hemolysis on two occasions after the administration of cephalosporin. On the first occasion, hemolysis was intravascular and was due to the formation of complexes between antibodies and the drug, which bound to red blood cells and caused severe hemolysis. On the second occasion, he...

    journal_title:Hematology (Amsterdam, Netherlands)

    pub_type: 杂志文章

    doi:

    authors: Malaponte G,Arcidiacono C,Mazzarino C,Pelligra S,Li Volti G,Bevelacqua V,Li Volti S

    更新日期:2000-01-01 00:00:00

  • Circulating thrombopoietin in clonal versus reactive thrombocytosis.

    abstract:INTRODUCTION:The aim of this study is to assess circulating thrombopoietin concentrations in patients with both clonal and reactive thrombocytosis (RT), which are two distinct categories of extreme platelet production circumstances. Investigation of the thrombopoietin levels in clonal versus reactive thrombocytosis may...

    journal_title:Hematology (Amsterdam, Netherlands)

    pub_type: 杂志文章

    doi:10.1080/10245330290020081

    authors: Karakuş S,Ozcebe OI,Haznedaroğlu IC,Göker H,Ozatli D,Koşar A,BüyükaşIk Y,Ertuğrul D,SayInalp N,KirazlI S,Dündar SV

    更新日期:2002-02-01 00:00:00

  • MCP-1, MIP-1, IL-8 and ischemic cerebral tissue enhance human bone marrow stromal cell migration in interface culture.

    abstract::Bone marrow stromal cells (MSCs) administered intravenously are effective in reducing neurological deficits after stroke in the rodent. These cells appear to selectively migrate and express neural phenotypes in ischemic brain. To elucidate the mechanisms targeting MSC migration into the ischemic brain, we measured, us...

    journal_title:Hematology (Amsterdam, Netherlands)

    pub_type: 杂志文章

    doi:10.1080/10245330290028588

    authors: Wang L,Li Y,Chen X,Chen J,Gautam SC,Xu Y,Chopp M

    更新日期:2002-04-01 00:00:00

  • Troxacitabine activity in extramedullary myeloid leukemia.

    abstract::Troxacitabine is a novel L-enantiomer nucleoside analog with unique properties in terms of its structure, pharmacokinetics, intracellular transport, and susceptibility to mechanisms of resistance. Troxacitabine has significant activity in patients with refractory myeloid leukemias, both as a single agent and when comb...

    journal_title:Hematology (Amsterdam, Netherlands)

    pub_type: 临床试验,杂志文章

    doi:10.1080/1024533021000008155

    authors: Alvarado Y,Kantarjian HM,Cortes JE,Apostolidou E,Bivins C,Giles FJ

    更新日期:2002-06-01 00:00:00

  • "Pawn Ball Megakaryocytes": from the marvellous medici and dear Old Saint Nick to the unsanctified marrow of myelodysplasia.

    abstract::The worlds of biology and medicine in general, and the discipline of hematology in particular, enjoy a rich lexicon full of fascinating etymologies. The term "Pawn Ball Megakaryocytes" has been used to describe a peculiar type of abnormal cell that can be found in bone marrow samples taken from some patients with the ...

    journal_title:Hematology (Amsterdam, Netherlands)

    pub_type: 传,历史文章,杂志文章

    doi:10.1080/1024533031000081397

    authors: Steensma DP

    更新日期:2003-02-01 00:00:00

  • c-Myc oncogene and Cdc25A cell activating phosphatase expression in non-Hodgkin's lymphoma.

    abstract:UNLABELLED:The product of proto-oncogene c-Myc is a potent activator of cell proliferation. The prognostic importance of the over expression of c-Myc and its transcriptional target Cdc25A in non-Hodgkin lymphoma (NHL) patients remains to be elucidated. To determine the role and the prognostic relevance of c-Myc and Cdc...

    journal_title:Hematology (Amsterdam, Netherlands)

    pub_type: 杂志文章

    doi:10.1080/1024533031000090829

    authors: Aref S,Fouda M,El-Dosoky E,Menessy A,Mabed M,Saleeb M,Zalata K

    更新日期:2003-06-01 00:00:00

  • Eradication of invasive mucormycosis--effectiveness of the Echinocandin FK463.

    abstract:BACKGROUND:Invasive rhinocerebral mucormycosis is a rare and often fatal opportunistic fungal infection. It is encountered in immunocompromised hosts exemplified by those with diabetes, human immunodeficiency viruses and particularly haematologic malignancies typically after high-dose chemotherapy and stem cell transpl...

    journal_title:Hematology (Amsterdam, Netherlands)

    pub_type: 杂志文章

    doi:10.1080/1024533031000090810

    authors: Jacobs P,Wood L,Du Toit A,Esterhuizen K

    更新日期:2003-04-01 00:00:00

  • Evaluating the effectiveness of epoetin alfa in community oncology practices.

    abstract:PURPOSE:This retrospective case-series review studied the effectiveness of epoetin alfa in community oncology practices, which until now has not been well documented. METHODS:We reviewed the medical records of 118 cancer patients treated between 1999 and 2001 with cyclic chemotherapy plus epoetin alfa in 27 US communi...

    journal_title:Hematology (Amsterdam, Netherlands)

    pub_type: 杂志文章

    doi:10.1080/10245330310001594243

    authors: Harris Spiridonidis C,Brinkmannb K,Fridman M,Gupta S,Tannous RE

    更新日期:2003-08-01 00:00:00

  • Immune reconstitution and early infectious complications following nonmyeloablative hematopoietic stem cell transplantation.

    abstract::Non-myeloablative stem cell transplantation (NMT) has been increasingly used in compromised patients who would otherwise have been unable to undergo allotransplant. There is little understanding of the kinetics of immune reconstitution and its influence on infective complications following NMT. The aim of present stud...

    journal_title:Hematology (Amsterdam, Netherlands)

    pub_type: 杂志文章

    doi:10.1080/10245330310001612125

    authors: Busca A,Lovisone E,Aliberti S,Locatelli F,Serra A,Scaravaglio P,Omedè P,Rossi G,Cirillo D,Barbui A,Ghisetti V,Dall'Omo AM,Falda M

    更新日期:2003-10-01 00:00:00

  • Leukemia associated clonal expansion of TCR Vbeta subfamily T cells.

    abstract::The analysis of the T cell receptor (TCR) Vbeta repertoire is one of the most sensitive methods to identify the clonal expansion T cells which respond to tumor associated antigens. Recently, studies have focused on clonally expanded T cells from patients or normal donors induced by leukemia associated antigens in vivo...

    journal_title:Hematology (Amsterdam, Netherlands)

    pub_type: 杂志文章

    doi:10.1080/10245330310001621288

    authors: Li Y

    更新日期:2003-12-01 00:00:00

  • Enhanced neutrophil apoptosis in neutropenic patients with hepatosplenic schistosomiasis: evidence of serum Fas ligand.

    abstract::Enhanced neutrophil apoptosis has been reported in neutropenic hepatosplenic schistosomiasis. The shortening of neutrophil survival via apoptosis may explain the neutropenia that occur in these patients. However, the regulation of neutrophil apoptosis in hepatosplenic schistosomiasis has not been clearly defined. Neut...

    journal_title:Hematology (Amsterdam, Netherlands)

    pub_type: 杂志文章

    doi:10.1080/10245330310001652482

    authors: Aref S,El Refaei MF,Sakrana M,El-Nemre H

    更新日期:2004-02-01 00:00:00

  • A review of the molecular diagnosis of thalassemia.

    abstract::The thalassaemias are a major health problem, and approximately 1 in 14 of the population are carriers for one of the sub types. For the purpose of prevention and control of clinically severe disease, molecular diagnosis either pre-natally or ante natal with genetic counselling are increasingly important. The majority...

    journal_title:Hematology (Amsterdam, Netherlands)

    pub_type: 杂志文章,评审

    doi:10.1080/1024533021000024102

    authors: Gu X,Zeng Y

    更新日期:2002-08-01 00:00:00

  • Update on the treatment of disseminated intravascular coagulation.

    abstract::Disseminated intravascular coagulation (DIC) is characterized by an acute generalized, widespread activation of coagulation, which results in thrombotic complications, due to the intravascular formation of fibrin, as well as diffuse hemorrhages, due to the consumption of platelets and coagulation factors. In this revi...

    journal_title:Hematology (Amsterdam, Netherlands)

    pub_type: 杂志文章,评审

    doi:10.1080/1024533042000205504

    authors: Franchini M,Manzato F

    更新日期:2004-04-01 00:00:00

  • Granulocyte-macrophage colony stimulating factor: an adjuvant for cancer vaccines.

    abstract::Granulocyte-macrophage colony stimulating factor (GM-CSF) enhances immune responses by inducing the proliferation, maturation, and migration of dendritic cells, and the expansion and differentiation of B and T lymphocytes. There is significant data in pre-clinical animal models demonstrating the adjuvant effects of GM...

    journal_title:Hematology (Amsterdam, Netherlands)

    pub_type: 杂志文章,评审

    doi:10.1080/10245330410001701549

    authors: Chang DZ,Lomazow W,Joy Somberg C,Stan R,Perales MA

    更新日期:2004-06-01 00:00:00

  • Immune tolerance therapy in patients with acquired hemophilia.

    abstract::Acquired hemophilia is a rare disorder with an estimated annual incidence of 0.2-1 cases per million individuals. The etiology of the disorder remains obscure, although approximately half of all cases are associated with other underlying conditions. In acquired hemophilia, the severe hemorrhagic diathesis is caused by...

    journal_title:Hematology (Amsterdam, Netherlands)

    pub_type: 杂志文章,评审

    doi:10.1080/10245330410001722087

    authors: von Depka M

    更新日期:2004-08-01 00:00:00

  • The haematology of indigenous Australians.

    abstract::Prior to European settlement indigenous Australians were hunter-gatherers who lived in geographically isolated small clan groups, also separated by elaborate totemic rules. Today they still reside in isolated communities throughout Australia but many have moved to the cities. They share a high incidence of a range of ...

    journal_title:Hematology (Amsterdam, Netherlands)

    pub_type: 杂志文章,评审

    doi:10.1080/10245330410001714176

    authors: Erber WN,Buck AM,Threlfall TJ

    更新日期:2004-10-01 00:00:00

  • Fatal thrombocytopaenia temporally related to the administration of alemtuzumab (MabCampath) for refractory CLL despite early discontinuation of therapy.

    abstract::Alemtuzumab (Campath 1H -MabCampath), initially used for prophylaxis of graft versus host disease in allogenic transplantaion, is now increasingly used for refractory chronic lymphatic leukaemia (CLL). Its efficacy has been well documented in this--the commonest form of leukaemia. Alemtuzumab is associated with severe...

    journal_title:Hematology (Amsterdam, Netherlands)

    pub_type: 杂志文章

    doi:10.1080/10245330400001942

    authors: Haider I,Cahill M

    更新日期:2004-10-01 00:00:00

  • Apoptosis and immaturity in acute myeloid leukemia.

    abstract::The primary cause of treatment failures in acute myeloid leukemia (AML) is the emergence of both resistant disease and early relapse. Among the most frequent agents of these phenomena are defects in the mitochondrial-mediated apoptotic pathway. This pathway is regulated by bcl-2 family of anti-apoptotic (bcl-2, bcl-xl...

    journal_title:Hematology (Amsterdam, Netherlands)

    pub_type: 杂志文章,评审

    doi:10.1080/10245330400020454

    authors: Del Principe MI,Del Poeta G,Venditti A,Buccisano F,Maurillo L,Mazzone C,Bruno A,Neri B,Irno Consalvo M,Lo Coco F,Amadori S

    更新日期:2005-02-01 00:00:00

  • Survey of hematological aspects of Gaucher disease.

    abstract::Hematologists have classically been the treating physicians of patients with Gaucher disease, and today, despite both specific and symptomatic therapeutic advances, they remain at the forefront of specialists to whom patients with Gaucher disease present. It is therefore appropriate to review that has changed and what...

    journal_title:Hematology (Amsterdam, Netherlands)

    pub_type: 杂志文章,评审

    doi:10.1080/10245330500067181

    authors: Zimran A,Altarescu G,Rudensky B,Abrahamov A,Elstein D

    更新日期:2005-04-01 00:00:00

  • NK-cell neoplasms in Japan.

    abstract::Neoplasms putatively originating from precursor and mature natural killer (NK) cells are rare, and their clinical features are unclear. A nationwide survey was performed in Japan to clarify the clinical features of these neoplasms diagnosed between 1994 and 1998, and data for 237 patients who met the criteria for puta...

    journal_title:Hematology (Amsterdam, Netherlands)

    pub_type: 杂志文章

    doi:10.1080/10245330400026162

    authors: Oshimi K,Kawa K,Nakamura S,Suzuki R,Suzumiya J,Yamaguchi M,Kameoka J,Tagawa S,Imamura N,Ohshima K,Kojya S,Iwatsuki K,Tokura Y,Sato E,Sugimori H,NK-cell Tumor Study Group.

    更新日期:2005-06-01 00:00:00

  • Recent thymic output function in patients with hematological malignancy.

    abstract::Thymic function is important for the generation of T-cell diversity in the periphery of both children and adults during both health and disease. Until recently, thymic function could not be monitored, as a consequence of the absence of adequate technology to differentiate recent thymic emigrants (RTEs) from naïve T ce...

    journal_title:Hematology (Amsterdam, Netherlands)

    pub_type: 杂志文章,评审

    doi:10.1080/10245330500093591

    authors: Li Y

    更新日期:2005-08-01 00:00:00

  • Amplification and overexpression of CKS1B at chromosome band 1q21 is associated with reduced levels of p27Kip1 and an aggressive clinical course in multiple myeloma.

    abstract::The molecular basis for aggressive transformation of multiple myeloma (MM) and other cancers is not completely understood. Global gene expression profiling on highly purified malignant plasma cells from 351 newly diagnosed patients with MM treated with autologous stem cell transplantation revealed a statistically sign...

    journal_title:Hematology (Amsterdam, Netherlands)

    pub_type: 杂志文章

    doi:10.1080/10245330512331390140

    authors: Shaughnessy J

    更新日期:2005-01-01 00:00:00

  • Treatment of Epstein-Barr virus--associated lymphoproliferative disorder (EBV-PTLD) and pure red cell aplasia (PRCA) with Rituximab following unrelated cord blood transplantation: a case report and literature review.

    abstract:OBJECTIVE:We report the first case of EBV-PTLD and pure red cell aplasia (PRCA) after an unrelated cord blood transplant in China, who was successfully treated with Rituximab. METHODS:Case report and literature review. RESULTS:A 5-year-old girl with CML underwent a major ABO-incompatible HLA-identical unrelated cord ...

    journal_title:Hematology (Amsterdam, Netherlands)

    pub_type: 杂志文章

    doi:10.1080/10245330410001714202

    authors: Zhu K,Chen J,Chen S

    更新日期:2005-10-01 00:00:00