174 results on '"Ducrocq, R."'
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2. Short insertion in a hemoglobin chain: Hb Esch, an unstable α1 variant with duplication of the sequence Ala 65-Leu-Thr-Asn 68
3. Purification, amplification and characterization of a population of human erythroid progenitors
4. A new alpha chain variant Hb Sallanches [alpha 2 104(G11) Cys --> Tyr] associated with HbH disease in one homozygous patient
5. Dépistage néonatal ciblé de la drépanocytose : bilan de cinq années d’expérience dans le nord-francilien
6. Strategy linking several analytical methods of neonatal screening for sickle cell disease
7. Syndromes drépanocytaires atypiques : à propos de deux cas
8. Separation of Nonenzymatically Glycosylated Proteins by Phenylboronate Affinity Chroma Tography
9. Haemoglobinopathies: a pitfall in the assessment of glycosylated haemoglobin by ion-exchange chromatography
10. Caractérisation phénotypique et moléculaire de deux syndromes drépanocytaires atypiques
11. L’annonce du diagnostic de syndrome drépanocytaire majeur chez un nouveau-né
12. Effect of transfusion therapy on cerebral vasculopathy in children with sickle-cell anemia
13. Modulation of erythroid adhesion receptor expression by hydroxyurea in children with sickle cell disease
14. Hétérogénéité génotypique du déficit en G6PD à l’Ouest de l’Afrique Sub-saharienne
15. Hétérogénéité génotypique du déficit en G6PD à l’Ouest de l’Afrique Sub-saharienne
16. Short insertion in a hemoglobin chain: Hb Esch, an unstable α1 variant with duplication of the sequence Ala65-Leu-Thr-Asn68
17. Le dépistage néonatal de la drépanocytose en France métropolitaine
18. Two NewGγ Chain Variants: Hb F-Clamart [γ17(A14)Lys→Asn] and Hb F-Ouled Rabah [γ19(B1)Asn→Lys]
19. A novel C→A transversion within the distal CCAAT motif of theGγ-globin gene in the algerianGγβ+-hereditary persistence of fetal hemoglobin
20. Molecular Basis of beta-Thalassemia in Bahrain: An Epicenter for a Middle East Specific Mutationa
21. Compound heterozygosity Hb S/Hb Hope (β136Gly→Asp): a pitfall in the newborn screening for sickle cell disease
22. Uremia and HbA1c Measured by High-Performance Liquid Chromatography
23. Gamma Chain Heterogeneity: Determination of Hb F Composition by Perfusion Chromatography
24. Determination of Hb F Levels: The Routine Methods
25. Three-Year Follow-Up of Hydroxyurea Treatment in Severely Ill Children with Sickle Cell Disease
26. NEWBORN SCREENING FOR SICLE CELL DISEASE IN FRANCE. 523
27. Variation of fetal hemoglobin and F-cell number with the LCR-HS2 polymorphism in nonanemic individuals [letter]
28. Perfusion chromatography allows an order of magnitude faster measurement of the G gamma: A gamma ratio in patients with an increased level of fetal hemoglobin [letter]
29. La drepanocytose a cotonou: Realites et perspectives
30. A new α chain variant Hb Sallanches [α2 104(G11) Cys→Tyr] associated with HbH disease in one homozygous patient
31. Bicentric origin of sickle hemoglobin among the inhabitants of Mauritius Island [letter]
32. Two Fetal Hemoglobin Variants Affecting the Same Residue: HB F-Emirates [Gγ59(E3)LYS→GLU] and HB F-Sacromonte [Gγ59(E3)LYS→GLN]
33. Variation in fetal hemoglobin parameters and predicted hemoglobin S polymerization in sickle cell children in the first two years of life: Parisian Prospective Study on Sickle Cell Disease
34. Beta-globin gene cluster haplotype and alpha-thalassemia do not correlate with the acute clinical manifestations of sickle cell disease in children [letter]
35. Measurement of Adult Hemoglobin in Fetal Blood Samples by High-Performance Liquid Chromatography as Purity Control for the Prenatal Diagnosis of Chromosomal Abnormalities
36. Foetal haemoglobin in normal healthy adults: relationship with polymorphic sequences cis to the β globin gene.
37. Two New Gγ Chain Variants: Hb F-Clamart [γ17(A14)Lys→Asn] and Hb F-Ouled Rabah [γ19(B1)Asn→Lys].
38. A novel C→A transversion within the distal CCAAT motif of the Gγ-globin gene in the algerian Gγβ+-hereditary persistence of fetal hemoglobin.
39. Two Fetal Hemoglobin Variants Affecting the Same Residue: HB F-Emirates [Gγ59(E3)LYS→GLU] and HB F-Sacromonte [Gγ59(E3)LYS→GLN].
40. Special Management of Insulin Lispro in Continuous Subcutaneous Insulin Infusion in Young Diabetic Children: A Randomized Cross-Over Study
41. Two New Gγ Chain Variants: Hb F-Clamart [γ17(A14)Lys→Asn] and Hb F-Ouled Rabah [γ19(B1)Asn→Lys]
42. Evaluation of the Tosoh HLC-723GHb V A1c 2.2 Hemoglobin A1c Analyzer
43. A novel C→A transversion within the distal CCAAT motif of the Gγ-globin gene in the algerian Gγβ+-hereditary persistence of fetal hemoglobin
44. The relative importance of the X-linked FCP locus and beta-globin haplotypes in determining haemoglobin F levels: a study of SS patients homozygous for betaS haplotypes
45. New Myanmar middle Eocene anthropoids. An Asian origin for catarrhines?
46. Molecular Basis of β-Thalassemia in Bahrain: An Epicenter for a Middle East Specific Mutationa.
47. Variation in fetal hemoglobin parameters and predicted hemoglobin S polymerization in sickle cell children in the first two years of life: Parisian prospective study on sickle cell disease
48. Importation route of the sickle cell trait into Portugal: contribution of molecular epidemiology
49. The role of the G6PD A-376G/968C allele in glucose-6-phosphate dehydrogenase deficiency in the Seerer population of Senegal
50. Evidence for nonenzymic glycation of antithrombin III in diabetic patients.
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