Search Results - "ITALIA, K."

Hyperimmunoglobulin syndrome due to CD40 deficiency: possibly the first case from India by Mishra, A, Italia, K, Gupta, M, Desai, M, Madkaikar, M

“…Hyperimmunoglobulin M (HIGM) type 3 due to CD40 deficiency is a very rare syndrome. Only 16 cases have been reported thus far. The clinical presentation is…”
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Identification of high oxygen affinity hemoglobin (Hb Andrew‐Minneapolis) in an Indian family by Mehta, P., Upadhye, D., Hariharan, P., Italia, K., Sawant, P., Nadkarni, A., Subramanian, G., Mukherjee, M. B.

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A successful twin pregnancy in a patient with HbE-β-thalassemia in western India by Merchant, R, Italia, K, Ahmed, J, Ghosh, K, Colah, R B

“…Improvements in medical facilities have helped a large number of clinically severe hemoglobin E (HbE)-β-thalassemia patients reach adulthood. Consequently,…”
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Hemoglobin Lepore Hollandia in India by NADKARNI, A., ITALIA, K., SAWANT, P., GHOSH, K., COLAH, R.

“…Summary Introduction:  Hb Lepore is a structurally abnormal hemoglobin in which the abnormal globin chain is a hybrid or fused δβ globin chain. In the…”
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HPLC studies in hemoglobinopathies by Colah, R B, Surve, R, Sawant, P, D'Souza, E, Italia, K, Phanasgaonkar, S, Nadkarni, A H, Gorakshakar, A C

“…An accurate diagnosis of beta -thalassemia carriers, homozygous patients and identification of different structural hemoglobin variants is important for…”
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Clinical and molecular characterization of Hb Hofu in eastern India by Purohit, P., Mashon, R. S., Patel, S., Dehury, S., Pattanayak, C., Das, K., Nair, S., Italia, K., Bag, S., Colah, R., Patel, D. K.

“…Summary Introduction Hb Hofu (HBB:c. 380T>A) is a rare inherited hemoglobin abnormality with few case reports in the world literature. Methods Screening for…”
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Hemoglobin variants in Muslim community in South Gujarat, Western India by Bhukhanvala, D. S., Sorathiya, S., Surve, R., Nair, S., Italia, K., Colah, R., Ghosh, K., Gupte, S. C.

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Evaluation of F cells in sickle cell disorders by flow cytometry - comparison with the Kleihauer-Betke's slide method by ITALIA, K. Y., COLAH, R., MOHANTY, D.

“…Summary Adult F cell numbers are raised in inherited haemoglobin disorders, such as β‐thalassaemia and sickle cell anaemia, hereditary persistence of foetal…”
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A successful twin pregnancy in a patient with HbE-[beta]-thalassemia in western India by Merchant, R, Italia, K, Ahmed, J, Ghosh, K, Colah, R

“…Improvements in medical facilities have helped a large number of clinically severe hemoglobin E (HbE)-β-thalassemia patients reach adulthood. Consequently,…”
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Hydroxyurea in sickle cell disease—A study of clinico-pharmacological efficacy in the Indian haplotype by Italia, Khushnooma, Jain, Dipty, Gattani, Sushma, Jijina, Farah, Nadkarni, Anita, Sawant, Pratibha, Nair, Sona, Mohanty, Dipika, Ghosh, Kanjaksha, Colah, Roshan

“…There is clinical variability in the presentation of sickle cell disease among Indians. Vaso-occlusive crisis is common among non-tribal patients. Hydroxyurea,…”
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Hemoglobin variants in M uslim community in S outh G ujarat, W estern I ndia by Bhukhanvala, D. S., Sorathiya, S., Surve, R., Nair, S., Italia, K., Colah, R., Ghosh, K., Gupte, S. C.

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Clinical and molecular characterization of H b H ofu in eastern I ndia by Purohit, P., Mashon, R. S., Patel, S., Dehury, S., Pattanayak, C., Das, K., Nair, S., Italia, K., Bag, S., Colah, R., Patel, D. K.

“…Summary Introduction H b H ofu ( HBB :c. 380T>A) is a rare inherited hemoglobin abnormality with few case reports in the world literature. Methods Screening…”
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HPLC Studies in Hemoglobinopathies : Newer Diagnostic Tests by COLAH, R. B, SURVE, R, SAWANT, P, D'SOUZA, E, ITALIA, K, PHANASGAONKAR, S, NADKARNI, A. H, GORAKSHAKAR, A. C

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Identification of high oxygen affinity hemoglobin (Hb Andrew-Minneapolis) in an Indian family by Mehta, P, Upadhye, D, Hariharan, P, Italia, K, Sawant, P, Nadkarni, A, Subramanian, G, Mukherjee, M B

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