17 results on '"Sharma, Prashant"'
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2. Automated alkaline-pH electrophoresis followed by densitometry does not correlate with cation-exchange (CE)-HPLC in quantification of HbA2 and variant hemoglobins.
3. First reported co‐occurrence of "GATA1‐mutated X‐linked thrombocytopenia with thalassemia (XLTT)" with heterozygous β‐thalassemia.
4. Hematological and genetic profiles of persons with co‐inherited heterozygous β‐thalassemia and supernumerary α‐globin genes.
5. Non-deletional haemoglobin H (Hb H) disease morphologically masquerading as congenital dyserythropoietic anaemia type II: a diagnostic pitfall.
6. A randomized controlled trial comparing the efficacy, tolerability, and cost of oral iron preparations in iron‐deficiency anemia in pregnancy.
7. Hb Mizuho (HBB: c.206T>C): Pitfalls of Screening Tests in an Unstable Hemoglobin Variant Diagnosed after Targeted Next-Generation Sequencing.
8. De novo haemoglobin sabine masquerading as double heterozygosity for HbQ-India and ß-thalassemia trait: first report from South Asia.
9. β -Thalassemia Intermedia Caused by Compound Heterozygosity for Hb Lepore-Hollandia and β -Thalassemia is Rare in the Indian Population.
10. HbQ-India (HBA1:c.193G>C): hematological profiles and unique CE-HPLC findings of potential diagnostic utility in 65 cases.
11. β-Thalassemia mutations in subjects with borderline HbA 2 values: a pilot study in North India.
12. Automated alkaline-pH electrophoresis followed by densitometry does not correlate with cation-exchange (CE)-HPLC in quantification of HbA2 and variant hemoglobins.
13. Hb M-Iwate in an Indian family.
14. False-positive negative control in a direct antiglobulin test.
15. A novel ATRX splice variant causing acquired HbH disease in myelodysplastic syndrome with excess blasts-1.
16. Performance analysis of machine learning algorithms and screening formulae for β-thalassemia trait screening of Indian antenatal women.
17. Homozygous KLF1 mutation c.901C>T (p.Arg301Cys) resulting in mild thalassemia intermedia in an Indian: A next-generation sequencing diagnosis.
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