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Khushnooma Italia

Showing results (1-10 of 16) with videos related to

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Plos One|December 19, 2013
Hydroxyurea could be a good clinically relevant iron chelatorKhushnooma Italia, Roshan Colah, Kanjaksha Ghosh
Blood Cells, Molecules & Diseases|August 1, 2015
Experimental animal model to study iron overload and iron chelation and review of other such modelsKhushnooma Italia, Roshan Colah, Kanjaksha Ghosh
Free Radical Research|July 7, 2016
Can hydroxyurea serve as a free radical scavenger and reduce iron overload in β-thalassemia patients?Khushnooma Italia, S Chandrakala, Kanjaksha Ghosh, et al.
Indian Pediatrics|June 26, 2012
Sickle cell anemia from central India: a retrospective analysisDipty Jain, Khushnooma Italia, Vijaya Sarathi, et al.
Prenatal Diagnosis|May 4, 2012
Prenatal diagnosis of HbE-Lepore and Hb Lepore-β-thalassemia: the importance of accurate genotyping of the couple at riskKhushnooma Italia, Jayesh Sheth, Pratibha Sawant, et al.
Hemoglobin|September 15, 2016
Hb E-β-Thalassemia in Five Indian StatesKhushnooma Italia, Pooja Dabke, Pratibha Sawant, et al.
European Journal of Haematology|June 14, 2012
Variable haematological and clinical presentation of β-thalassaemia carriers and homozygotes with the Poly A (T→C) mutation in the Indian populationKhushnooma Italia, Pratibha Sawant, Reema Surve, et al.
Annals of Hematology|May 14, 2013
Molecular characterization of β-thalassemia in four communities in South Gujarat--codon 30 (G → A) a predominant mutation in the Kachhiya Patel communityDipal S Bhukhanvala, Khushnooma Italia, Pratibha Sawant, et al.
Indian Journal of Human Genetics|September 11, 2013
Comparison of in-vitro and in-vivo response to fetal hemoglobin production and γ-mRNA expression by hydroxyurea in HemoglobinopathiesKhushnooma Italia, Farah Jijina, Rashid Merchant, et al.
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion|August 22, 2018
Prenatal Diagnosis of HbE-β-Thalassemia: Experience of a Center in Western IndiaRoshan Colah, Anita Nadkarni, Ajit Gorakshakar, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Plos One|December 19, 2013
Hydroxyurea could be a good clinically relevant iron chelatorKhushnooma Italia, Roshan Colah, Kanjaksha Ghosh
Blood Cells, Molecules & Diseases|August 1, 2015
Experimental animal model to study iron overload and iron chelation and review of other such modelsKhushnooma Italia, Roshan Colah, Kanjaksha Ghosh
Free Radical Research|July 7, 2016
Can hydroxyurea serve as a free radical scavenger and reduce iron overload in β-thalassemia patients?Khushnooma Italia, S Chandrakala, Kanjaksha Ghosh, et al.
Indian Pediatrics|June 26, 2012
Sickle cell anemia from central India: a retrospective analysisDipty Jain, Khushnooma Italia, Vijaya Sarathi, et al.
Prenatal Diagnosis|May 4, 2012
Prenatal diagnosis of HbE-Lepore and Hb Lepore-β-thalassemia: the importance of accurate genotyping of the couple at riskKhushnooma Italia, Jayesh Sheth, Pratibha Sawant, et al.
Hemoglobin|September 15, 2016
Hb E-β-Thalassemia in Five Indian StatesKhushnooma Italia, Pooja Dabke, Pratibha Sawant, et al.
European Journal of Haematology|June 14, 2012
Variable haematological and clinical presentation of β-thalassaemia carriers and homozygotes with the Poly A (T→C) mutation in the Indian populationKhushnooma Italia, Pratibha Sawant, Reema Surve, et al.
Annals of Hematology|May 14, 2013
Molecular characterization of β-thalassemia in four communities in South Gujarat--codon 30 (G → A) a predominant mutation in the Kachhiya Patel communityDipal S Bhukhanvala, Khushnooma Italia, Pratibha Sawant, et al.
Indian Journal of Human Genetics|September 11, 2013
Comparison of in-vitro and in-vivo response to fetal hemoglobin production and γ-mRNA expression by hydroxyurea in HemoglobinopathiesKhushnooma Italia, Farah Jijina, Rashid Merchant, et al.
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion|August 22, 2018
Prenatal Diagnosis of HbE-β-Thalassemia: Experience of a Center in Western IndiaRoshan Colah, Anita Nadkarni, Ajit Gorakshakar, et al.
Pageof 2