Impact of functional IL-18 polymorphisms on genetic predisposition and diverse clinical manifestations of the disease in Indian SLE patients von Umare, V, Pradhan, V, Nath, S, Rajadhyaksha, A, Ghosh, K, Nadkarni, AH

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Detection of fetal mutations causing hemoglobinopathies by non-invasive prenatal diagnosis from maternal plasma von D′Souza, E, Sawant, P, Nadkarni, A, Gorakshakar, A, Ghosh, K, Colah, R

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Expression of the matrix metalloproteinases MMP-2 and MMP-9 and their inhibitors TIMP-1 and TIMP-2 in systemic lupus erythematosus patients von Vira, H. J., Pradhan, V. D., Umare, V. D., Chaudhary, A. K., Rajadhyksha, A. G., Nadkar, M. Y., Ghosh, K., Nadkarni, A. H.

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Hemoglobin variants and high-performance liquid chromatography von Nair, S, Nadkarni, A. H., Ghosh, K., Colah, R.

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HPLC studies in hemoglobinopathies von Colah, R B, Surve, R, Sawant, P, D'Souza, E, Italia, K, Phanasgaonkar, S, Nadkarni, A H, Gorakshakar, A C

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Potential of denaturing gradient gel electrophoresis for scanning of β‐thalassemia mutations in India von Gorakshakar, A.C., Pawar, A.R., Nadkarni, A.H., Lu, C.Y., Mohanty, D., Krishnamoorthy, R., Besmond, C., Colah, R.B.

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Genetic Disorders in Haematological Practice in India von Mohanty, D., Colah, R.B., Gorakshakar, A.C., Nadkarni, A.H., Phanasgaonkar, S.P., Shetty, S., Ghosh, K., Mukherjee, M.B.

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Alpha Genotyping in a Heterogeneous Indian Population von Nadkarni, Anita H., Gorakshakar, Ajit C., Mohanty, Dipika, Colah, Roshan B.

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Beta-thalassaemia heterozygotes with alpha-globin gene triplication von Colah, R B, Nadkarni, A H, Mukherjee, M B, Gorakshakar, A C, Surve, R, Mohanty, D

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Prenatal Diagnosis of β-Thalassemia Among Indians using Denaturing Gradient Gel Electrophoresis von Gorakshakar, A. C., Lulla, C. P., Nadkarni, A. H., Pawar, A. R., Desai, S. N., Colah, R. B., Mohanty, D.

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Invasive & non-invasive approaches for prenatal diagnosis of haemoglobinopathies: experiences from India von Colah, R B, Gorakshakar, A C, Nadkarni, A H

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Hemoglobin E and Pyrimidine 5' Nucleotidase Deficiency von Nadkarni, AH, Ghosh, K, Mohanty, D, Colah, R

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Clinical, hematologic and molecular variability of sickle cell-β thalassemia in western India von Mukherjee, Malay B, Nadkarni, Anita H, Gorakshakar, Ajit C, Ghosh, Kanjaksha, Mohanty, Dipika, Colah, Roshan B

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HPLC Studies in Hemoglobinopathies : Newer Diagnostic Tests von COLAH, R. B, SURVE, R, SAWANT, P, D'SOUZA, E, ITALIA, K, PHANASGAONKAR, S, NADKARNI, A. H, GORAKSHAKAR, A. C

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Congenital methemoglobinemia caused by Hb‐M Ratnagiri (β‐63CAT→TAT, His→Tyr) in an Indian family von Kedar, Prabhakar S., Nadkarni, Anita H., Phanasgoankar, Supriya, Madkaikar, Manisha, Ghosh, Kanjaksha, Gorakshakar, Ajit C., Colah, Roshan B., Mohanty, Dipika

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Hemoglobin E and pyrimidine 5' nucleotidase deficiency von Nadkarni, A H, Ghosh, K, Mohanty, D, Colah, R

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Usefulness of automated chromatography for rapid fetal blood analysis for second trimester prenatal diagnosis of β-thalassemia von Wadia, Mahrukh R., Phanasgaokar, Supriya P., Nadkarni, Anita H., Surve, Reema R., Gorakshakar, Ajit C., B. Colah, Roshan, Mohanty, Dipika

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Detection of Rare β-Thalassemia Mutations by Denaturing Gradient Gel Electrophoresis Among Indians von Gorakshakar, Ajit C., Phanasgaonkar, Supriya P., Nadkarni, Anita H., Colah, Roshan B., Mohanty, Dipika

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Prenatal Diagnosis in a Family at Risk for β-Thalassemia and Hemophilia A: An Uncommon Association von Colah, Roshan B., Shetty, Shrimati D., Surve, Reema R., Phanasgaonkar, Supriya P., Nadkarni, Anita H., Gorakshakar, Ajit C., Ghosh, Kanjaksha, Parekh, Sunil J., Mohanty, Dipika

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Global epidemiology of pediatric severe sepsis: the sepsis prevalence, outcomes, and therapies study von Weiss, Scott L, Fitzgerald, Julie C, Pappachan, John, Wheeler, Derek, Jaramillo-Bustamante, Juan C, Salloo, Asma, Singhi, Sunit C, Erickson, Simon, Roy, Jason A, Bush, Jenny L, Nadkarni, Vinay M, Thomas, Neal J

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