1. A pair of twin girls suffered from thalassemia major.

2. Methods: Using man - vessel screen method of thalassemia and relative value of G6PD detect thalassemia and G6PD deficiency for man and woman of detection of before marriage in 4268 duplet .

3. Methods: Using mon-vessel screen method of thalassemia and relative value of G6PD detect thalassemia and G6PD deficiency for man and woman of detection of before marriage in 4268 duplet.

4. Objective To investigate the carrier rate of thalassemia gene in children with decreased mean corpuscular volume(MCV).

5. Mediterranean anemia(thalassemia), occurring relatively often in southern China, is a genetic and hemolytic disease induced by disfunction of globin synthesis.

6. Diseases such as sickle cell anemia and beta thalassemia result from abnormal red blood cells and can be treated with bone-marrow transplants.

7. Objectives To evaluate the early diagnosis way of thalassemia major.

8. Free erythrocyte Protoporphyrin(FEP)were determined in 116 thalassemia patients, 37 iron deficiency anemia patients and 45 normal subjects.

9. Thalassemia is considered a kind of heritable hemolytic disease with high heterology.

10. He was also informed that, due to thalassemia gene deletion or mutation is caused by, but not its genetic transmission.

11. Objective To determine value of chorionic villus sampling ( CVS ) in early diagnosis of severe thalassemia.

12. We found 10 types of rnutation and 28 com - pound genotypes of ? ? - thalassemia.

13. Recently, the team reported the first case of successful non-myeloablative matched unrelated stem cell transplantation in a thalassemia major patient.

14. The cause of the liver cirrhosis was considered to be due to iron overload resulting from thalassemia.

15. Objective To investigate the incidence and types of genic mutations for thalassemia in Shenzhen area and perform the prenatal diagnosis in high risk fetus.

16. The medicines now under threat are for childcare, in the maternity departments, and for conditions such as cancer, epilepsy, haemophilia and thalassemia.

17. Objective To explore the value of red blood cell parameters (MCV/RDW) and red blood cell morphology combined detection in thalassemia diagnosis.

18. Other anemias. There are several other, rarer forms of anemia, such as thalassemia and anemias caused by defective hemoglobin.

19. The case followed complaints by families of some 170 people, many of them children, suffering from haemophilia and the blood disease thalassemia.

20. OBJECTIVE: To study the status of iron metabolism and erythropoietic proliferation in children with various genotypes of thalassemia.

21. Human umbilical cord blood (UCB) has plenty of hematopoietic stem cells (HSCs) and can be used in the cure of leukaemia, malignancy and thalassemia major.

22. Objective:To study the relationship between mean corpuscular volume(MCV), mean corpuscular hemoglobin(MCH) of umbilical blood and thalassemia.

23. To study the types and frequency of gene mutations of ? ? - thalassemia in Jiangxi area.

24. Objective:To approach the value and applicability of the activity of Glucose-6-phosphate dehydrogenase (G6PD) for the auxiliary diagnosis of thalassemia.

25. Objective: To study the rate of the combined tests of thalassemia and G6PD deficiency in detection of before marriage, to direct aristogenesis and good brood.

26. Secondary or acquired hemochromatosis can be caused by diseases such as thalassemia or sideroblastic anemia, especially if the person has received a large number of blood transfusions.

27. ObjectiveTo explore the changes of reticulocyte multiple parameters and their clinical significance in patients with thalassemia minor.

28. Objective: To evaluate the safety and efficacy of combining deferiprone(DFP)and deferoxamine(DFO)in iron chelation therapy in patients with thalassemia.

29. Conclusion The simple and quick blood test, in particular, MCV, RDW of iron deficiency anemia and thalassemia clinical identification, have some diagnostic value,(/thalassemia.html) should be applied.