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94 results on '"G 6 pd deficiency"'

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1. HIV and Glucose-6-Phosphate Dehydrogenase (G-6-PD) Deficiency among University Athletes in Rivers State, Nigeria

2. Therapeutic whole blood exchange in the management of methaemoglobinemia: Case series and systematic review of literature

3. Prevalence of Glucose -6- Phosphate Dehydrogenase (G-6-PD) Deficiency in Sokoto: Liver Function and Oxidative Stress Biomarkers in Deficient Individual

4. Blood Groups, Hemoglobinopathy and G-6-PD Deficiency Investigations Among Fifteen Major Scheduled Tribes of Orissa, India

5. Cyclic Seasonal Variation of G-6-PD Deficiency in Newborn Infants from Sardinia

6. Investigação genético-epidemiológica e molecular da deficiência de G-6-PD em uma comunidade brasileira

7. Sickle Cell Haemoglobin and Glucose-6- Phosphate Dehydrogenase Deficiency among the Rajputs of Dadra and Nagar Haveli

8. Comparison for functional aberration of G-6-PD deficiency variants with exon 10 mutations

9. HAART has no major impact on hematological and plasma bilirubin changes in HIV-infected patients with congenital G-6-PD deficiency

10. Case 41

11. Assessment of the Prevalence of Glucose-6-Phosphate Dehydrogenase (G-6-PD) Deficiency among Patients in Harare

12. Glucose‐6‐phosphate dehydrogenase deficiency, neonatal tetanus and neonatal jaundice in Nigeria: Clinical observation

13. Prevalence and Pattern of Glucose-6-Phosphate Dehydrogenase Deficiency in Different Haemoglobin Types in Ile-Ife

14. Application of a new chemiluminescence method for the determination of glucose-6-phosphate dehydrogenase activity in healthy and enzyme-deficient individuals

15. Knowledge and misconceptions about sickle cell anemia and glucose-6-phosphate dehydrogenase deficiency among adult sickle cell anemia patients in al Qatif Area (eastern KSA)

17. Coinheritance of Rotor syndrome, G-6-PD deficiency, and heterozygous beta thalassemia: a possible genetic interaction

18. Prevalence of G-6-PD deficiency in the Croatian Adriatic Coast population

21. Effect of G-6 PD deficiency on sickle cell disease in Saudi Arabia

25. Glucotoxicity and Oxidathre Hemolysis in G-6-PD Deficiency

30. Hemoglobin A1 in Subjects with G-6-PD Deficiency During and After Hemolytic Crises Due to Favism

31. Septicémie à Yersinia enterocolitica chez un diabétique porteur d'une double hémoglobinopathie

32. Agar in Control of Hyperbilirubinemia of Full-Term Newborn Infants with Erythrocyte G-6-PD Deficiency

33. Frequency of Glucose-6-Phosphate Dehydrogenase Deficiency in Sickle-Cell Disease

34. Three Years Experience in Preventing Severe Hyperbilirubinemia in Newborn Infants with Erythrocyte G-6-PD Deficiency

35. Separate detection of glucose-6-phosphate dehydrogenase from 6-phosphogluconate dehydrogenase by DEAE-paper chromatography

36. Biochemische Eigenschaften einer neuen Variante des Glucose-6-phosphatdehydrogenase (G-6-PD)-Mangels mit Favismus: G-6-PD Bielefeld

37. Salicylamide Glucuronide Formation in Newborn Babies with G-6-PD Deficiency

38. An evaluation of the dorset sheep as a predictive animal model for the response of G‐6‐PD deficient human erythrocytes to a proposed systemic toxic ozone intermediate, methyl linoleate hydroperoxide

39. Glucose-6-Phosphate Dehydrogenase Ferrara

40. Favism and Hemolytic Anemia in Glucose-6-Phosphate Dehydrogenase-Deficient Subjects in North Sardinia

41. Etude sur la distribution de la déficience en G.-6-P.D. en Sardaigne

42. Salicylamide-Glucuronide Formation in Children with Favism and in Their Parents

43. Low Incidence of Erythrocyte G-6-PD Deficiency in Koreans

44. Evaluation of Glucose-6-Phosphate Dehydrogenase in Single Erythrocytes in Human Blood Smears

45. Glucose-6-Phosphate Dehydrogenase Toulouse

46. Genetic Studies of the Seneca Indians: Haptoglobins, Transferrins, G-6-PD Deficiency, Hemoglobinopathy, Color Blindness, Morphological Traits and Dermatoglyphics

47. EFFECT OF OROTIC ACID UPON SERUM BILIRUBIN IN NEWBORN INFANTS WITH ERYTHROCYTE G-6-PD DEFICIENCY

48. G-6-PD Deficiency and Abnormal Hemoglobins in a Brazilian Population

49. THE NORMAL HUMAN FEMALE AS A MOSAIC OF X-CHROMOSOME ACTIVITY: STUDIES USING THE GENE FOR G-6-PD-DEFICIENCY AS A MARKER

50. International Committee for Standardization in Haematology: Recommended Screening Test for Glucose-6-Phosphate Dehydrogenase (G-6-PD) Deficiency

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