45 results on '"Moumni, Imen"'
Search Results
2. Emotional and behavioral attitudes of Tunisian youth towards childhood leukemia: health education and primary prevention in perspective
3. For a Better Literacy of Tunisians in Eco-health: Leishmaniasis Case
4. For a Better Literacy of Tunisians in Eco-health: Leishmaniasis Case
5. Coinheritance of HbO Arab/β 0 -thalassemia with Severe Manifestation in Newborn.
6. TP53 Gene 72 Arg/Pro (rs1042522) single nucleotide polymorphism increases the risk and the severity of chronic lymphocytic leukemia
7. PHINDaccess Hackathons for COVID-19 and Host-Pathogen Interaction: Lessons Learned and Recommendations for Low- and Middle-Income Countries
8. PB2543: CIRCULATING MICROVESICLES AS POTENTIAL CELLULAR BIOMARKERS FOR THROMBOTIC RISKS IN BETA THALASSEMIA
9. Association of rs1319868, rs1567811 and rs8041224 of IGF1R gene with infection among sickle cell anemia Tunisian patients
10. The New Epidemiological Challenges of the Tunisian School: Are We Ready?
11. Molecular characterization of a novel homozygous deletion in β-globin cluster causing (δβ)0-Thalassemia among Tunisian family
12. Fetal Hemoglobin in Tunisian Sickle Cell Disease Patient: Relationship with Polymorphic Sequences Cis to the β-Globin Gene
13. Two new class III G6PD variants [G6PD Tunis (c.920A > C: p.307Gln > Pro) and G6PD Nefza (c.968T > C: p.323 Leu > Pro)] and overview of the spectrum of mutations in Tunisia
14. Molecular characterization of a novel homozygous deletion in β-globin cluster causing (δβ) 0 -Thalassemia among Tunisian family.
15. Coinheritance of HbO Arab/β0-thalassemia with Severe Manifestation in Newborn
16. Association of Lymphotoxin Alpha Polymorphism with Type 1 Diabetes in a Tunisian Population
17. Infectious disease risk perception among Tunisian students: a case study of Leishmaniasis
18. Empowering Tunisian School Students to Prevent Food and Zoonotic Diseases
19. Abstracts from the 3rd International Genomic Medicine Conference (3rd IGMC 2015)
20. Restriction mapping of βS locus among tunisian sickle-cell patients
21. The role of rs1984112_G atCD36gene in increasing reticulocyte level among sickle cell disease patients
22. rs11886868 and rs4671393 of BCL11A associated with HbF level variation and modulate clinical events among sickle cell anemia patients
23. Early complication in Sickle Cell Anemia children due to A(TA)_n TAA polymorphism at the promoter of UGT1A1 gene
24. rs11886868 and rs4671393 ofBCL11Aassociated with HbF level variation and modulate clinical events among sickle cell anemia patients
25. Two new β+-thalassemia mutation [β -56 (G → C); HBBc. −106 G → C] and [β −83 (G → A); HBBc. −133 G → A] described among the Tunisian population
26. Fetal Hemoglobin in Tunisian Sickle Cell Disease Patient: Relationship with Polymorphic Sequences Cis to the β-Globin Gene
27. The role of rs1984112_G at CD36 gene in increasing reticulocyte level among sickle cell disease patients.
28. A New δ Chain Variant, Hb A2-Tunis [δ46(CD5)Gly → Glu;HBD: c.140G>A], Observed in a Tunisian Family in Association with a Compound Heterozygosity for Hb C [β6(A3)Glu → Lys;HBB: c.19G>A] β0-Thalassemia [IVS-I-1 (β143, G>A);HBB: c.92+1G>A]
29. Haplotype Map of Sickle Cell Anemia in Tunisia
30. Association of Lymphotoxin Alpha Polymorphism with Type 1 Diabetes in a Tunisian Population
31. Two new class III G6PD variants [G6PD Tunis (c.920A>C: p.307Gln>Pro) and G6PD Nefza (c.968T>C: p.323 Leu>Pro)] and overview of the spectrum of mutations in Tunisia
32. Early Complication in Sickle Cell Anemia Children due toA(TA)nTAAPolymorphism at the Promoter ofUGT1A1Gene
33. Implication of genetic variation at the promoter and exon1 of UGT1A1 in occurrence of cholelithiasis in Tunisia
34. Microsatellite and Single Nucleotide Polymorphisms in the β-Globin Locus Control Region-Hypersensitive Site 2: Specificity of Tunisian βSChromosomes
35. Molecular characterization of a discrete hemoglobinopathy upon investigation for a lung hydatic cyst in an old Tunisian patient
36. Hb A2-Pasteur-Tunis [δ59(E3)Lys→Asn, AAG→AAC]: A New δ Chain Variant Detected by DNA Sequencing in a Tunisian Carrier of the Codon 39 (C→T) β0-Thalassemia Mutation
37. Two new β+-thalassemia mutation [ β -56 (G → C); HBBc. −106 G → C] and [ β −83 (G → A); HBBc. −133 G → A] described among the Tunisian population.
38. Association of rs1319868, rs1567811 and rs8041224 of IGF1Rgene with infection among sickle cell anemia Tunisian patients
39. Early Complication in Sickle Cell Anemia Children due to A(TA)n TAA Polymorphism at the Promoter of UGT1A1 Gene.
40. Microsatellite and Single Nucleotide Polymorphisms in the β-Globin Locus Control Region-Hypersensitive Site 2: Specificity of Tunisian βS Chromosomes.
41. A New δ Chain Variant, Hb A2-Tunis [δ46(CD5)Gly → Glu; HBD: c.140G>A], Observed in a Tunisian Family in Association with a Compound Heterozygosity for Hb C [β6(A3)Glu → Lys; HBB: c.19G>A] β0-Thalassemia [IVS-I-1 (β143, G>A); HBB: c.92+1G>A]
42. Coinheritance of HbO Arab/β0-thalassemia with Severe Manifestation in Newborn.
43. A new δ chain variant, Hb A2-Tunis [δ46(CD5)Gly → Glu; HBD: c.140G>A], observed in a Tunisian family in association with a compound heterozygosity for Hb C [β6(A3)Glu → Lys; HBB: c.19G>A] β(0)-thalassemia [IVS-I-1 (β143, G>A); HBB: c.92+1G>A].
44. Early complication in Sickle Cell Anemia children due to A(TA)<formula>_n</formula> TAA polymorphism at the promoter of UGT1A1 gene.
45. Hb A2-Pasteur-Tunis [delta59(E3)Lys-->Asn, AAG-->AAC]: a new delta chain variant detected by DNA sequencing in a Tunisian carrier of the codon 39 (C-->T) beta0-Thalassemia mutation.
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