Laboratory diagnosis of hemoglobinopathies.
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[1] D J Weatherall,et al. The thalassemia syndromes. , 2016, Texas reports on biology and medicine.
[2] H. Witkowska,et al. Electrospray mass spectrometry in the clinical diagnosis of variant hemoglobins. , 1991, Journal of chromatography.
[3] S. Binder,et al. An automated system for sickle cell screening. , 1990, American clinical laboratory.
[4] H. Witkowska,et al. Tandem mass spectrometry in the clinical analysis of variant hemoglobins. , 1990, Rapid communications in mass spectrometry : RCM.
[5] M. Mann,et al. Electrospray ionization for mass spectrometry of large biomolecules. , 1989, Science.
[6] K. Pass,et al. Cellulose acetate/citrate agar electrophoresis of filter paper hemolysates from heel stick. , 1989, Pediatrics.
[7] H. Pearson. Sickle cell trait and competitive athletics: is there a risk? , 1989, Pediatrics.
[8] T. Peto,et al. Deferoxamine inhibition of malaria is independent of host iron status , 1988, The Journal of experimental medicine.
[9] E. Vichinsky,et al. Newborn screening for sickle cell disease: effect on mortality. , 1988, Pediatrics.
[10] E. Kanavakis,et al. CORRELATION OF CLINICAL PHENOTYPE TO GENOTYPE IN HAEMOGLOBIN H DISEASE , 1988, The Lancet.
[11] D. Simel. Is the RDW-MCV classification of anaemia useful? , 1987, Clinical and laboratory haematology.
[12] J. Kark,et al. Sickle-cell trait as a risk factor for sudden death in physical training. , 1987, The New England journal of medicine.
[13] G. Lucarelli,et al. Marrow transplantation in patients with advanced thalassemia. , 1987, The New England journal of medicine.
[14] M. Steinberg,et al. Alpha-thalassemia in blacks: genetic and clinical aspects and interactions with the sickle hemoglobin gene. , 1986, Blood.
[15] T. Huisman,et al. Rapid cation-exchange high-performance liquid chromatographic procedure for the separation and quantitation of hemoglobins S, C, and O Arab in cord blood samples. , 1986, The Journal of laboratory and clinical medicine.
[16] Y. Kan,et al. Survival of a hydropic infant with homozygous α-thalassemia-1 , 1986 .
[17] John T. Wilson,et al. The effect of Hb F and α‐thalassemia on the red cell indices in sickle cell anemia , 1986 .
[18] H. T. Milhorn,et al. Gross hematuria in a patient with sickle cell trait. , 1985, Postgraduate medicine.
[19] Y. Kan. Molecular Pathology of α‐Thalassemia , 1985 .
[20] A. Cohen,et al. Treatment of Iron Overload in Cooley's Anemia a , 1985, Annals of the New York Academy of Sciences.
[21] D. Labie,et al. Hematologically and genetically distinct forms of sickle cell anemia in Africa. The Senegal type and the Benin type. , 1985, The New England journal of medicine.
[22] S. Schrier,et al. Erythrocyte membrane alterations in beta-thalassaemia. , 1985, Clinics in haematology.
[23] R. J. Hayes,et al. The haematology of steady state homozygous sickle cell disease: frequency distributions, variation with age and sex, longitudinal observations , 1985, British journal of haematology.
[24] C. Rodeck,et al. EFFECT OF FETAL DIAGNOSTIC TESTING ON BIRTH-RATE OF THALASSAEMIA MAJOR IN BRITAIN , 1984, The Lancet.
[25] W. Schroeder,et al. High Performance Liquid Cbromatographic Separation of Globin Chains on a Large-Pore C4 Column , 1984 .
[26] H. Bunn,et al. Hemoglobin: Molecular, Genetic and Clinical Aspects , 1984 .
[27] T. Ley,et al. Advances in thalassemia research. , 1984, Blood.
[28] D. Labie,et al. Evidence for the multicentric origin of the sickle cell hemoglobin gene in Africa. , 1984, Proceedings of the National Academy of Sciences of the United States of America.
[29] R. Spritz,et al. The thalassemias: molecular mechanisms of human genetic disease. , 1983, American journal of human genetics.
[30] B. Lubin,et al. Anemia and hemoglobinopathies in Southeast Asian refugee children. , 1983, The Journal of pediatrics.
[31] S. Embury,et al. Hematologic improvement following splenectomy for hemoglobin-H disease. , 1982, The Western journal of medicine.
[32] S. Ballas,et al. Clinical, hematological, and biochemical features of Hb SC disease , 1982, American journal of hematology.
[33] J. Clegg,et al. The interaction of alpha-thalassemia and homozygous sickle-cell disease. , 1982, The New England journal of medicine.
[34] Julian R. E. Davis,et al. Concurrent Sickle-Cell Anemia and α-Thalassemia: Effect on Severity of Anemia , 1982 .
[35] T. Coates,et al. Molecular analysis of the beta-thalassemia phenotype associated with inheritance of hemoglobin E (alpha 2 beta2(26)Glu leads to Lys). , 1981, The Journal of clinical investigation.
[36] W. Trager,et al. The biochemistry of resistance to malaria. , 1981, Scientific American.
[37] Y. Beuzard,et al. Cord blood screening for hemoglobin abnormalities by thin layer isoelectric focusing. , 1980, Blood.
[38] V. Fairbanks,et al. Homozygous hemoglobin E mimics β‐thalassemia minor without anemia or hemolysis: Hematologic, functional, and biosynthetic studies of first north American cases , 1980 .
[39] L. Luzzatto. Genetics of red cells and susceptibility to malaria , 1979 .
[40] P. Lanzkowsky,et al. Leukocyte counts in children with sickle cell disease. , 1979, American journal of diseases of children.
[41] G. Serjeant,et al. Comparison of Sickle Cell‐β° Thalassaemia with Homozygous Sickle Cell Disease , 1979 .
[42] P. Basset,et al. Isoelectric focusing of human hemoglobin: its application to screening, to the characterization of 70 variants, and to the study of modified fractions of normal hemoglobins. , 1978, Blood.
[43] B. Glader,et al. Leukocyte counts in children with sickle cell disease. Comparative values in the steady state, vaso-occlusive crisis, and bacterial infection. , 1978, American journal of diseases of children.
[44] B. Lubin,et al. The influence of plasma bilirubin on zinc protoporphyrin measurement by a hematofluorimeter. , 1978, The Journal of laboratory and clinical medicine.
[45] J. Lawrence,et al. Localization of the human α-globin structural gene to chromosome 16 in somatic cell hybrids by molecular hybridization assay , 1977, Cell.
[46] S. Karpatkin,et al. Elevated platelet count and megathrombocyte number in sickle cell anemia. , 1975, Blood.
[47] J. Bowman,et al. Hemoglobin E, an oxidatively unstable mutation. , 1975, The Journal of laboratory and clinical medicine.
[48] M. Jeannet,et al. Letter: HL-A antigens in asymptomatic chronic HBAg carriers. , 1974, Lancet.
[49] G. Serjeant,et al. The Clinical Features of Haemoglobin SC Disease in Jamaica , 1973, British journal of haematology.
[50] P. Milner,et al. The clinical features of sickle-cell- thalassaemia in Jamaica. , 1973, British journal of haematology.
[51] P. Wolf,et al. Automated dithionite test for rapid, inexpensive detection of hemoglobin S and non-S sickling hemoglobinopathies. , 1971, Clinical chemistry.
[52] R. Gunn,et al. Thalassemia: the consequences of unbalanced hemoglobin synthesis. , 1966, The American journal of medicine.
[53] A. Chernoff,et al. Studies on abnormal hemoglobins. I. Their demonstration in sickle cell anemia and other hematologic disorders by means of alkali denaturation. , 1951, Blood.
[54] D. Rao,et al. Age and prevalence of sickle‐cell trait in a large ambulatory population , 1987, Genetic epidemiology.
[55] A. Kutlar,et al. Separation of normal and abnormal hemoglobin chains by reversed-phase high-performance liquid chromatography. , 1986, Journal of chromatography.
[56] K. Lanclos,et al. The thalassemia repository. , 1986, Hemoglobin.
[57] S. Karlsson,et al. Developmental regulation of human globin genes. , 1985, Annual review of biochemistry.
[58] R. Nussbaum,et al. Morbidity of sickle cell trait at high altitude. , 1984, Southern medical journal.
[59] N. Mohandas,et al. Concurrent sickle cell anemia and alpha-thalassemia. Effect on pathological properties of sickle erythrocytes. , 1984, The Journal of clinical investigation.
[60] E. Vichinsky,et al. Multidisciplinary approach to pain management in sickle cell disease. , 1982, The American journal of pediatric hematology/oncology.
[61] R. Schneider,et al. Hemoglobin mobility in citrate agar electrophoresis - its relationship to anion binding. , 1982, Hemoglobin.
[62] W. Vainchenker,et al. Beta O-thalassemia/Hb E association. Hemoglobin synthesis in blood reticulocytes and bone marrow cells fractionated by density gradient and in blood erythroid colonies in culture. , 1980, Acta haematologica.
[63] J. Jereb,et al. Hemoglobin E trait reexamined: a cause of microcytosis and erythrocytosis. , 1979, Blood.
[64] G. E. Simon,et al. The measurement of free erythrocyte porphyrin (FEP) as a simple means of distinguishing iron deficiency from beta-thalassemia trait in subjects with microcytosis. , 1975, The Journal of laboratory and clinical medicine.