663 results on '"Colah, Roshan"'
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2. Defining global strategies to improve outcomes in sickle cell disease: a Lancet Haematology Commission
3. Significance of borderline HbA2 levels in β thalassemia carrier screening
4. Wide spectrum of novel and rare hemoglobin variants in the multi‐ethnic Indian population: A review.
5. Casting light on the national mission to eliminate sickle cell disease in India.
6. Genotypic-phenotypic heterogeneity of δβ-thalassemia and hereditary persistence of fetal hemoglobin (HPFH) in India
7. Haemoglobinopathies in India: estimates of blood requirements and treatment costs for the decade 2017–2026
8. Red Cell Indices and Hemoglobin Profile of Newborn Babies with Both the Sickle Gene and Alpha Thalassaemia in Central India
9. Genetic lesions in the UGT1A1 genes among Gilbert’s syndrome patients from India
10. Burden of thalassemia in India: The road map for control
11. Clinico-Hematological Presentation of Rare Hemoglobin Variant (HB-O Indonesia) in 3 Families
12. Prenatal Diagnosis of HbE-β-Thalassemia: Experience of a Center in Western India
13. First Observation of Hb Lepore Hollandia in the Baiga Tribal Family
14. Red Cell Distribution Width (RDW): Normative Data in Indian Neonates
15. The spatial epidemiology of sickle-cell anaemia in India
16. Experimental animal model to study iron overload and iron chelation and review of other such models
17. Tyrosine kinase inhibitors: New class of antimalarials on the horizon?
18. Synergistic effect of two β globin gene cluster mutations leading to the hereditary persistence of fetal hemoglobin (HPFH) phenotype
19. Spectrum of β-Thalassemia and Other Hemoglobinopathies in the Saurashtra Region of Gujarat, India: Analysis of a Large Population Screening Program
20. Obituary: Professor Sir David John Weatherall GBE, MD, FRCP, FRS
21. Sickle Cell Disease in Central India: A Potentially Severe Syndrome
22. Correlation between ‘H’ blood group antigen and Plasmodium falciparum invasion
23. Five Rare β Globin Chain Hemoglobin Variants in India
24. Diverse phenotypes and transfusion requirements due to interaction of β-thalassemias with triplicated α-globin genes
25. Molecular Heterogeneity of Hb H Disease in India
26. Role of Oxidative Stress and the Protective Effect of Fermented Papaya Preparation in Sickle Cell Disease
27. Molecular and clinical heterogeneity in pyruvate kinase deficiency in India
28. Effect of a group of genetic markers around the 5′ regulatory regions of the β globin gene cluster linked to high HbF on the clinical severity of β thalassemia
29. Prevalence of clinically relevant (TA)n UGT1A1 promoter alleles in Indian neonates
30. Genetic Variations in Bilirubin Metabolism Genes and Their Association with Unconjugated Hyperbilirubinemia in Adults
31. Phenotypic diversity of sickle cell disorders: a rebuttal
32. Influence of single nucleotide polymorphisms in the BCL11A and HBS1L-MYB gene on the HbF levels and clinical severity of sickle cell anaemia patients
33. Newborn Screening for Sickle Cell Disease Among Tribal Populations in the States of Gujarat and Madhya Pradesh in India: Evaluation and Outcome Over 6 Years
34. Thalassemia in India
35. Does HbF induction by hydroxycarbamide work through MIR210 in sickle cell anaemia patients?
36. Challenges in prenatal diagnosis of beta thalassaemia: couples with normal HbA2 in one partner
37. Do UGT1A1 and HMOX1 gene promoter polymorphisms increase the risk of hyperbilirubinemia and gallstones in patients with hereditary spherocytosis?
38. Spectrum of red cell abnormalities in undiagnosed hemolytic anemias and methemoglobinemias: a single center experience
39. The Prevalence of Factor V Leiden (GI69IA) and Methylenetetrahydrofolate Reductase C677T Mutations in Sickle Cell Disease in Western India
40. Variable phenotypes of sickle cell disease in India with the Arab-Indian haplotype
41. Regional heterogeneity of β-thalassemia mutations in the multi ethnic Indian population
42. Hydroxyurea in sickle cell disease—A study of clinico-pharmacological efficacy in the Indian haplotype
43. Response to hydroxyurea in β thalassemia major and intermedia: Experience in western India
44. Molecular characterization of β-thalassemia in four communities in South Gujarat—codon 30 (G → A) a predominant mutation in the Kachhiya Patel community
45. Efficacy of fixed low dose hydroxyurea in Indian children with sickle cell anemia: A single centre experience
46. Newborn screening for haemoglobinopathies by high performance liquid chromatography (HPLC): diagnostic utility of different approaches in resource-poor settings
47. Antenatal Screening for Identification of Couples for Prenatal Diagnosis of Severe Hemoglobinopathies in Surat, South Gujarat
48. Cascade screening for β-thalassemia: A practical approach for identifying and counseling carriers in India
49. Hereditary non-spherocytic hemolytic anemia and severe glucose phosphate isomerase deficiency in an Indian patient homozygous for the L487F mutation in the human GPI gene
50. Is Cellulose Acetate Electrophoresis a Suitable Technique for Detection of Hb Bart's at Birth?
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