...Sandro Trova; Paolo Mereu; Elena Cocco; Bruno Masala; Laura Manca; Monica Pirastru During a screening for hemoglobinopathies, we found a carrier of the Sardinian δβ-thalassemia condition. The proband's hematology and hemoglobin (Hb) profile agreed with those of the other carriers previously...

... and hemoglobinopathies have been conducted [ 4,5 ]. Our results confirm that the prevalence of thalassemia is particularly high for both α-thal and β-thal, as well as for Hb E. Compared to previous studies conducted in the Vientiane Prefecture, the prevalence values of all forms of α-thal including α⁰-thal, α + -thal...

... analysis using combined HPLC and capillary electrophoresis did help in the initial recognition and in making presumptive diagnoses, but definite diagnoses of these cases with complex α- and β-hemoglobinopathies could only be obtained after DNA analysis. Table 1 lists the hematological findings...

.... Anemia Hemoglobinopathies Iron deficiency Thalassemia Vietnam Anemia is a serious public health problem, especially in developing countries. A number of factors might contribute to the condition but generally it is assumed that iron deficiency (ID) is the major cause [ 1,2 ]. However, ID...

...–48.1%) of the study participants. The overall proportion of thalassemia and hemoglobinopathies was 56.4% (95% CI = 49.8–62.9%). Of the anemic participants, 45.4% had ID. Based on the receiver-operating characteristic curve analysis, 4 formulas were applicable for predicting ID among anemic individuals...

... of iron deficiency, thalassemia and combined thalassemia and iron deficiency among anemic subjects were 10.2, 53.8 and 30.8% in Mukdahan, and 7.7, 67.3 and 9.6% in Roi-Et. Hematological characteristics were analyzed and are presented. It is concluded that thalassemia and hemoglobinopathies rather than...

... Haplotypes Hemoglobinopathies Pediatric hematology Prognosis Sickle cell anemia Sickle cell anemia (SCA) is an autosomal recessive disease characterized by the homozygous state of hemoglobin S [Hb S; 6(A1) Glu→Val], which is a variant hemoglobin resulting from a β-globin gene mutation (HBB:c.20A...

...R. Cabannes; A. Sendrail; C. Bouloux; E. Carles-Trochain The results of a first investigation on hemoglobins of Maya Indians of the Yucatan Peninsula in Mexico are set out. This investigation confirms the very inferquent occurrence of hemoglobinopathy among the Indians of the American continent...

... and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements. Hemoglobin M Hemoglobinopathies Hereditary methemoglobinemia Acta Haemat. 47: 225-232 (1972) Congenital...

...(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements. Hemoglobin J Paris Hemoglobinopathies Acta haemat. 47: 43-48 (1972) Hemoglobin J Paris («12 Alanine-*Aspartic Acid...

... and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements. Hb Gα Georgia Hb S-Gα Georgia Hemoglobin interactions Hemoglobinopathies Sickle cell anemia Acta Haemat. 51: 315...

.... Hemoglobin F persistence Hemoglobinopathies Thalassemia Acta Haemat. 50: 124-128 (1973) Hereditary Persistence of Fetal Hemoglobin and Thalassemia in a Turkish Child B. Yamak, S. Ozsoylu, A ltay, G. HigsoNMEZ and B. Say Hacettepe University School of Medicine, Department of Pediatrics, and Hacettepe...

... Hemoglobinopathies Thalassemia Acta Haernat. 50: 184-190 (1973) Hemoglobin HThalassemia S. Ozsoylu, G. HigsdNMEz and C. Altay Hacettepe University School of Medicine and Hacettepe Children s Hospital Medical Center, Ankara Abstract. A Turkish child with Hb Hthalassemia Key Words and a clinical picture...

.... C. General Hospital, and the Department of Medicine, Georgetown University School of Medicine, Washington, D.C. Abstract. Red cell life span was measured in 5 subjects Key Words with sickle cell trait using both 31Cr and DF32P as red cell Hemoglobinopathies tags. All were otherwise normal except...

... to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements. Hb C Hb N-Baltimore Hemoglobinopathies Acta haemat. 56: 183-188 (1976) A Case with Both Hemoglobins C and N-Baltimore Cage J ohnson, D arleen Powars and W. A. Schroeder...

... Hemoglobinopathies Microchromatography Thalassemia screening β -Thalassemia Acta haemat. 57: 32-36 (1977) Quantitation of Hb A2with DE-52 Microchromatography in Whole Blood as Screening Test for Thalassemia Heterozygotes1 R. Galanello, M. A. M elis, P. M uroni and A. Cao Pediatric Clinic, University...

... to in the content or advertisements. Hemoglobin Beograd Hemoglobinopathies Thalassemia Acta haemat. 54: 180-187 (1975) Hemoglobin Beograd (a 121 GluVal) Interacting with Thalassemia1 R .R uvidió, G.D. Efremov, D. J urició, Z. Rolovió, 1. RuZDióand S. Pendió Internal Clinic B, Faculty of Medicine...

... of this study. A sickle cell trait frequency of 0.123 evidenced by hemoglobin electrophoresis correlates closely with previous studies of hemoglobinopathies in Saudi Arabs. The presence of four subjects with sickle cell disease in the study group provides further evidence of the ‘benign’ nature of sickle cell...

... or safety. The publisher and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements. Hemoglobinopathies Hb Camden Hb Hope Acta haemat. 54: 53-58 (1975) Hb Camden and Hb...

... and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements. Hemoglobin genes Hemoglobinopathies Hereditary persistence of Hb F Thalassemia Acta haemat. 56: 285-291 (1976...