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Roshan B Colah

Showing results (71-80 of 86) with videos related to

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American Journal of Hematology|June 2, 2005
Congenital methemoglobinemia caused by Hb-MRatnagiri (beta-63CAT-->TAT, His-->Tyr) in an Indian familyPrabhakar S Kedar, Anita H Nadkarni, Supriya Phanasgoankar, et al.
American Journal of Hematology|August 28, 2010
Hemolytic anemia and distal renal tubular acidosis in two Indian patients homozygous for SLC4A1/AE1 mutation A858DBoris E Shmukler, Prabhakar S Kedar, Prashant Warang, et al.
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|July 23, 2013
The Prevalence of Factor V Leiden (G1691A) and Methylenetetrahydrofolate Reductase C677T Mutations in Sickle Cell Disease in Western IndiaHarshada K Kangne, Farah F Jijina, Yazdi M Italia, et al.
Annals of Hematology|August 31, 2015
Diverse phenotypes and transfusion requirements due to interaction of β-thalassemias with triplicated α-globin genesPallavi R Mehta, Dipti S Upadhye, Pratibha M Sawant, et al.
American Journal of Clinical Pathology|August 22, 2019
Multicenter Evaluation of HemoTypeSC as a Point-of-Care Sickle Cell Disease Rapid Diagnostic Test for Newborns and Adults Across IndiaMalay B Mukherjee, Roshan B Colah, Pallavi R Mehta, et al.
Hemoglobin|September 8, 2022
Role of Oxidative Stress and the Protective Effect of Fermented Papaya Preparation in Sickle Cell DiseasePrashant P Warang, Nikhil S Shinde, Vinod D Umare, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 24, 2009
Response to hydroxyurea in beta thalassemia major and intermedia: experience in western IndiaKhushnooma Y Italia, Farah J Jijina, Rashid Merchant, et al.
Journal of Clinical Pathology|February 16, 2010
Effect of hydroxyurea on the transfusion requirements in patients with severe HbE-beta-thalassaemia: a genotypic and phenotypic studyKhushnooma Y Italia, Farah F Jijina, Rashid Merchant, et al.
Hemoglobin|April 8, 2021
The Changing Trends in Prenatal Diagnosis of Hemoglobinopathies in India: The Quest of a Single Center to Reduce the Burden of Disease over Three DecadesRoshan B Colah, Anita H Nadkarni, Ajit C Gorakshakar, et al.
Hemoglobin|January 22, 2005
Prenatal diagnosis in a family at risk for beta-thalassemia and hemophilia A: an uncommon associationRoshan B Colah, Shrimati D Shetty, Reema R Surve, et al.
Pageof 9

Showing results (71-80 of 86) with videos related to

Sort By:
Pageof 9
American Journal of Hematology|June 2, 2005
Congenital methemoglobinemia caused by Hb-MRatnagiri (beta-63CAT-->TAT, His-->Tyr) in an Indian familyPrabhakar S Kedar, Anita H Nadkarni, Supriya Phanasgoankar, et al.
American Journal of Hematology|August 28, 2010
Hemolytic anemia and distal renal tubular acidosis in two Indian patients homozygous for SLC4A1/AE1 mutation A858DBoris E Shmukler, Prabhakar S Kedar, Prashant Warang, et al.
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|July 23, 2013
The Prevalence of Factor V Leiden (G1691A) and Methylenetetrahydrofolate Reductase C677T Mutations in Sickle Cell Disease in Western IndiaHarshada K Kangne, Farah F Jijina, Yazdi M Italia, et al.
Annals of Hematology|August 31, 2015
Diverse phenotypes and transfusion requirements due to interaction of β-thalassemias with triplicated α-globin genesPallavi R Mehta, Dipti S Upadhye, Pratibha M Sawant, et al.
American Journal of Clinical Pathology|August 22, 2019
Multicenter Evaluation of HemoTypeSC as a Point-of-Care Sickle Cell Disease Rapid Diagnostic Test for Newborns and Adults Across IndiaMalay B Mukherjee, Roshan B Colah, Pallavi R Mehta, et al.
Hemoglobin|September 8, 2022
Role of Oxidative Stress and the Protective Effect of Fermented Papaya Preparation in Sickle Cell DiseasePrashant P Warang, Nikhil S Shinde, Vinod D Umare, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 24, 2009
Response to hydroxyurea in beta thalassemia major and intermedia: experience in western IndiaKhushnooma Y Italia, Farah J Jijina, Rashid Merchant, et al.
Journal of Clinical Pathology|February 16, 2010
Effect of hydroxyurea on the transfusion requirements in patients with severe HbE-beta-thalassaemia: a genotypic and phenotypic studyKhushnooma Y Italia, Farah F Jijina, Rashid Merchant, et al.
Hemoglobin|April 8, 2021
The Changing Trends in Prenatal Diagnosis of Hemoglobinopathies in India: The Quest of a Single Center to Reduce the Burden of Disease over Three DecadesRoshan B Colah, Anita H Nadkarni, Ajit C Gorakshakar, et al.
Hemoglobin|January 22, 2005
Prenatal diagnosis in a family at risk for beta-thalassemia and hemophilia A: an uncommon associationRoshan B Colah, Shrimati D Shetty, Reema R Surve, et al.
Pageof 9