604 results on '"ELION J."'
Search Results
2. P-052: LEVERAGING PLASMA-DERIVED EXOSOMES FOR BIOMARKER DISCOVERY IN SICKLE CELL DISEASE: PREPARATION FOR A LARGE PROSPECTIVE STUDY
3. Information, consentement et transfusion sanguine : compte rendu du 6e Séminaire d’éthique transfusionnelle de l’Institut national de la transfusion sanguine
4. DIVERSITY OF β-GLOBIN HAPLOTYPES IN SICKLE CELL DISEASE PATIENTS FROM BRAZIL
5. Comparative Study of Mycobacterium paratuberculosis Strains Isolated from Crohn's Disease and Johne's Disease Using Restriction Fragment Length Polymorphism and Arbitrarily Primed Polymerase Chain Reaction
6. Defining global strategies to improve outcomes in sickle cell disease: a Lancet Haematology commission
7. S126: AN EU -- ARISE INITIATIVE GAP ANALYSIS APPROACH TO IMPROVING THE QUALITY OF LABORATORY SYSTEMS IN SUB-SAHARAN AFRICA.
8. P135: THE CLINGEN HEMOGLOBINOPATHY VARIANT CURATION EXPERT PANEL
9. Complexity of Pseudomonas aeruginosa Infection in Cystic Fibrosis: Combined Results from Esterase Electrophoresis and rDNA Restriction Fragment Length Polymorphism Analysis
10. Molecular Analysis of Multiply Recurrent Meningitis Due to Escherichia coli K1 in an Infant
11. Erythroid adhesion molecules in sickle cell disease: Effect of hydroxyurea
12. DEFINIÇÃO DOS HAPLÓTIPOS DO GENE DA β-GLOBINA EM PACIENTES COM DOENÇA FALCIFORME DA REGIÃO SUDESTE DO BRASIL UTILIZANDO UM ENSAIO SNAPSHOT MULTIPLEX
13. LEVERAGING PLASMA-DERIVED EXOSOMES FOR BIOMARKER DISCOVERY IN SICKLE CELL DISEASE: PREPARATION FOR A LARGE PROSPECTIVE STUDY
14. Bases moléculaires et physiopathologiques des maladies de l'hémoglobine
15. Newborn screening for sickle cell disease in Europe
16. Identification of constitutional MT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation database
17. Molecular Analysis Provides Evidence for the Endogenous Origin of Bacteremia and Meningitis Due to Enterobacter cloacae in an Infant
18. Analysis of the 5′ flanking sequence of the Gγ globin gene by denaturing gradient gel electrophoresis confirms the heterogeneity of the Bantu βs haplotype
19. Molecular epidemiological analysis ofPseudomonas aeruginosa strains causing failure of antibiotic therapy in cystic fibrosis patients
20. A novel sickle cell mutation of yet another origin in Africa: the Cameroon type
21. Prevalence of SMN1 deletion and duplication in carrier and normal populations: implication for genetic counselling
22. Hydroxyurea downregulates endothelin-1 gene expression and upregulates ICAM-1 gene expression in cultured human endothelial cells
23. Anthropological approach to the heterogeneity of beta-thalassemia mutations in Northern Africa
24. Pharmacogénétique, étude du génome et développement des médicaments
25. Pharmacogenetic and Pharmacogenomic Studies
26. Iron overload in thalassaemias and genetic haemochromatosis
27. Prevalence of the G20210A Polymorphism in the 3′-Untranslated Region of the Prothrombin Gene in Different Human Populations
28. HLA-DQB 1 codon 57 and genetic susceptibility to Type 1 (insulin-dependent) diabetes mellitus in French children
29. Dépistage néonatal ciblé de la drépanocytose : bilan de cinq années d’expérience dans le nord-francilien
30. Purpura fulminans méningococcique : rencontre malheureuse de polymorphismes génétiques ?
31. Conversion of HIV-1 viral markers during the first few months of life in HlV-infected children born to seropositive mothers
32. Déficit constitutionnel en protéine B du surfactant pulmonaire: présentation clinique, diagnostic histologique et moléculaire
33. Identification par hybridation soustractive de régions chromosomiques spécifiques des souches de Escherichia coli responsables de méningites néonatales
34. Anthropological Approach to the Heterogeneity of ß-Thalassemia Mutations in Northern Africa
35. The european hematology association roadmap for european hematology research: A consensus document
36. The European Hematology Association Roadmap for European Hematology Research: a consensus document.
37. The european hematology association roadmap for european hematology research: A consensus document
38. Phenotypic and genetic heterogeneity of unexplained neonatal/early infantile respiratory distress in Reunion Island: SP-B deficiency and alveolar proteinosis
39. Drépanocytose et priapisme : rôle des paramètres hématologiques et hémorhéologiques
40. A rare FokI RFLP in the human dopamine D2 receptor gene (DRD2)
41. Haemoglobin D-Ouled Rabah among the Mozabites: A Relevant Variant to Trace the Origin of Berber-Speaking Populations
42. Strategy linking several analytical methods of neonatal screening for sickle cell disease
43. [Pathophysiology of sickle cell disease]
44. Syndromes drépanocytaires atypiques : à propos de deux cas
45. Separation of Nonenzymatically Glycosylated Proteins by Phenylboronate Affinity Chroma Tography
46. Purification and Characterization of the Rat Kidney and Cerebellum 28K Vitamin D-Dependent Calcium Binding Proteins
47. Haemoglobinopathies: a pitfall in the assessment of glycosylated haemoglobin by ion-exchange chromatography
48. Thrombin: Structural Features Related to Specificity1
49. Chromosome 22q13.3 deletion syndrome with a de novo interstitial 22q13.3 cryptic deletion disrupting SHANK3
50. Compound SFTPB 1549C--GAA (121ins2) and 457delC heterozygosity in severe congenital lung disease and surfactant protein B (SP-B) deficiency
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