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Roshan Colah

Showing results (51-60 of 57) with videos related to

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Genetic Testing|April 29, 2008
Carrier screening for beta-thalassemia during pregnancy in India: a 7-year evaluationRoshan Colah, Reema Surve, Marukh Wadia, et al.
Blood Cells, Molecules & Diseases|October 29, 2008
Hydroxyurea in sickle cell disease--a study of clinico-pharmacological efficacy in the Indian haplotypeKhushnooma Italia, Dipty Jain, Sushma Gattani, et al.
Indian Pediatrics|June 27, 2013
Efficacy of fixed low dose hydroxyurea in Indian children with sickle cell anemia: a single centre experienceDipti L Jain, Mohini Apte, Roshan Colah, et al.
Blood Cells, Molecules & Diseases|August 19, 2004
Impact of beta globin gene mutations on the clinical phenotype of beta thalassemia in IndiaRoshan Colah, Anita Nadkarni, Ajit Gorakshakar, et al.
British Journal of Haematology|March 17, 2010
Epidemiology of beta-thalassaemia in Western India: mapping the frequencies and mutations in sub-regions of Maharashtra and GujaratRoshan Colah, Ajit Gorakshakar, Supriya Phanasgaonkar, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 11, 2014
Clinical and hematological presentation among Indian patients with common hemoglobin variantsKhushnooma Italia, Dipti Upadhye, Pooja Dabke, et al.
Indian Journal of Human Genetics|November 18, 2014
Guidelines for screening, diagnosis and management of hemoglobinopathiesKanjaksha Ghosh, Roshan Colah, Mamta Manglani, et al.
Pageof 6

Showing results (51-60 of 57) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 57 results.
Genetic Testing|April 29, 2008
Carrier screening for beta-thalassemia during pregnancy in India: a 7-year evaluationRoshan Colah, Reema Surve, Marukh Wadia, et al.
Blood Cells, Molecules & Diseases|October 29, 2008
Hydroxyurea in sickle cell disease--a study of clinico-pharmacological efficacy in the Indian haplotypeKhushnooma Italia, Dipty Jain, Sushma Gattani, et al.
Indian Pediatrics|June 27, 2013
Efficacy of fixed low dose hydroxyurea in Indian children with sickle cell anemia: a single centre experienceDipti L Jain, Mohini Apte, Roshan Colah, et al.
Blood Cells, Molecules & Diseases|August 19, 2004
Impact of beta globin gene mutations on the clinical phenotype of beta thalassemia in IndiaRoshan Colah, Anita Nadkarni, Ajit Gorakshakar, et al.
British Journal of Haematology|March 17, 2010
Epidemiology of beta-thalassaemia in Western India: mapping the frequencies and mutations in sub-regions of Maharashtra and GujaratRoshan Colah, Ajit Gorakshakar, Supriya Phanasgaonkar, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 11, 2014
Clinical and hematological presentation among Indian patients with common hemoglobin variantsKhushnooma Italia, Dipti Upadhye, Pooja Dabke, et al.
Indian Journal of Human Genetics|November 18, 2014
Guidelines for screening, diagnosis and management of hemoglobinopathiesKanjaksha Ghosh, Roshan Colah, Mamta Manglani, et al.
Pageof 6