Search Results - "Panjwani, Sangeeta"

An AQP1 null allele in an Indian woman with Co(a-b-) phenotype and high-titer anti-Co3 associated with mild HDN by Joshi, Sanmukh R., Wagner, Franz F., Vasantha, K, Panjwani, Sangeeta R., Flegel, Willy A.

“…BACKGROUND: The Colton blood group system (CO, ISBT 015) is composed of three antigens, of which Co3 (ISBT 015.003) is carried by almost all persons, except…”
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Response to hydroxyurea in β thalassemia major and intermedia: Experience in western India by Italia, Khushnooma Y., Jijina, Farah J., Merchant, Rashid, Panjwani, Sangeeta, Nadkarni, Anita H., Sawant, Pratibha M., Nair, Sona B., Ghosh, Kanjaksha, Colah, Roshan B.

“…The clinical and hematological response to hydroxyurea was evaluated in β thalassemia patients in western India with variable clinical severity and correlated…”
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Effect of hydroxyurea on the transfusion requirements in patients with severe HbE-beta-thalassaemia: a genotypic and phenotypic study by Italia, Khushnooma Y, Jijina, Farah F, Merchant, Rashid, Panjwani, Sangeeta, Nadkarni, Anita H, Sawant, Pratibha M, Nair, Sona B, Ghosh, Kanjaksha, Colah, Roshan B

“…Haemoglobin E (HbE)-beta-thalassaemia has a very variable clinical presentation. The management of severe cases that are often transfusion dependent is similar…”
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