Neonatal Screening and the Clinical Outcome in Children with Sickle Cell Disease in Central India von Upadhye, Dipti S, Jain, Dipty L, Trivedi, Yogesh L, Nadkarni, Anita H, Ghosh, Kanjaksha, Colah, Roshan B

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The phenotypic and molecular diversity of hemoglobinopathies in India: A review of 15 years at a referral center von Nadkarni, Anita H., Gorakshakar, Ajit C., Sawant, Pratibha M., Italia, Khushnooma Y., Upadhye, Dipti S., Gorivale, Manju S., Mehta, Pallavi R., Hariharan, Priya, Ghosh, Kanjaksha, Colah, Roshan B.

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Diverse phenotypes and transfusion requirements due to interaction of β-thalassemias with triplicated α-globin genes von Mehta, Pallavi R., Upadhye, Dipti S., Sawant, Pratibha M., Gorivale, Manju S., Nadkarni, Anita H., Shanmukhaiah, Chandrakala, Ghosh, Kanjaksha, Colah, Roshan B.

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First case of Hb Fontainebleau with sickle haemoglobin and other non-deletional α gene variants identified in neonates during newborn screening for sickle cell disorders von Upadhye, Dipti S, Jain, Dipty, Nair, Sona B, Nadkarni, Anita H, Ghosh, Kanjaksha, Colah, Roshan B

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Newborn screening for haemoglobinopathies by high performance liquid chromatography (HPLC): diagnostic utility of different approaches in resource-poor settings von Upadhye, Dipti S., Jain, Dipty L., Trivedi, Yogesh L., Nadkarni, Anita H., Ghosh, Kanjaksha, Colah, Roshan B.

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Diverse phenotypes and transfusion requirements due to interaction of [beta]-thalassemias with triplicated [alpha]-globin genes von Mehta, Pallavi R, Upadhye, Dipti S, Sawant, Pratibha M, Gorivale, Manju S, Nadkarni, Anita H, Shanmukhaiah, Chandrakala, Ghosh, Kanjaksha, Colah, Roshan B

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First case of Hb Fontainebleau with sickle haemoglobin and other non-deletional [alpha] gene variants identified in neonates during newborn screening for sickle cell disorders von Upadhye, Dipti S, Jain, Dipty, Nair, Sona B, Nadkarni, Anita H, Ghosh, Kanjaksha, Colah, Roshan B

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First case of Hb Fontainebleau with sickle haemoglobin and other non-deletional α gene variants identified in neonates during newborn screening for sickle cell disorders von UPADHYE, Dipti S, JAIN, Dipty, NAIR, Sona B, NADKARNI, Anita H, GHOSH, Kanjaksha, COLAH, Roshan B

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Homozygous sickle cell disease in Central India & Jamaica: A comparison of newborn cohorts von Jain, Dipty, Tokalwar, Rajini, Upadhye, Dipti, Colah, Roshan, Serjeant, Graham

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Red Cell Indices and Hemoglobin Profile of Newborn Babies with Both the Sickle Gene and Alpha Thalassaemia in Central India von Upadhye, Dipti, Jain, Dipty, Nadkarni, Anita, Ghosh, Kanjaksha, Colah, Roshan

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Influence of single nucleotide polymorphisms in the BCL11A and HBS1L-MYB gene on the HbF levels and clinical severity of sickle cell anaemia patients von Upadhye, Dipti, Jain, Dipty, Trivedi, Yogesh, Nadkarni, Anita, Ghosh, Kanjaksha, Colah, Roshan

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Prenatal Diagnosis of HbE-β-Thalassemia: Experience of a Center in Western India von Colah, Roshan, Nadkarni, Anita, Gorakshakar, Ajit, Sawant, Pratibha, Italia, Khushnooma, Upadhye, Dipti, Gaikwad, Harshali, Ghosh, Kanjaksha

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Clinical and hematological presentation among Indian patients with common hemoglobin variants von Italia, Khushnooma, Upadhye, Dipti, Dabke, Pooja, Kangane, Harshada, Colaco, Stacy, Sawant, Pratibha, Nadkarni, Anita, Gorakshakar, Ajit, Jain, Dipty, Italia, Yazdi, Ghosh, Kanjaksha, Colah, Roshan

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