Molecular pathology of rare bleeding disorders (RBDs) in India: a systematic review von Kulkarni, Bipin P, Nair, Sona B, Vijapurkar, Manasi, Mota, Leenam, Shanbhag, Sharda, Ali, Shehnaz, Shetty, Shrimati D, Ghosh, Kanjaksha

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Detection of a novel mutation in NLRP3/CIAS1 gene in an Indian child with Neonatal-Onset Multisystem Inflammatory Disease (NOMID) von Nair, Sona B., Chavan, Pallavi Pimpale, Athalye, Arundhati S., Aksentijevich, Ivona, Khubchandani, Raju P.

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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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Response to hydroxyurea in β thalassemia major and intermedia: Experience in western India von Italia, Khushnooma Y., Jijina, Farah J., Merchant, Rashid, Panjwani, Sangeeta, Nadkarni, Anita H., Sawant, Pratibha M., Nair, Sona B., Ghosh, Kanjaksha, Colah, Roshan B.

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Effect of hydroxyurea on the transfusion requirements in patients with severe HbE-β-thalassaemia: a genotypic and phenotypic study von Italia, Khushnooma Y, Jijina, Farah F, Merchant, Rashid, Panjwani, Sangeeta, Nadkarni, Anita H, Sawant, Pratibha M, Nair, Sona B, Ghosh, Kanjaksha, Colah, Roshan B

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Molecular Diversity of Hemoglobin H Disease in India von NADKARNI, Anita H, NAIR, Sona B, ITALIA, Khushnooma Y, WARANG, Prashant, DALVI, Madhura, GHOSH, Kanjaksha, COLAH, Roshan B

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Molecular Pathology of Rare Bleeding Disorders von Kulkarni, Bipin P, Nair, Sona B, Vijapurkar, Manasi, Mota, Leenam, Shanbhag, Sharda, Ali, Shehnaz, Shetty, Shrimati D, Ghosh, Kanjaksha

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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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Glanzmann's thrombasthenia von TULLU, Milind S, DIXIT, Prashant S, NAIR, Sona B, KAMAT, Jaishree R, VASWANI, Rajwanti K, SHETTY, Shrimati D, PAWAR, Aruna R

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Effect of hydroxyurea on the transfusion requirements in patients with severe HbE-[beta]-thalassaemia: a genotypic and phenotypic study von Italia, Khushnooma Y, Jijina, Farah F, Merchant, Rashid, Panjwani, Sangeeta, Nadkarni, Anita H, Sawant, Pratibha M, Nair, Sona B, Ghosh, Kanjaksha, Colah, Roshan B

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Research update for articles published in EJCI in 2010 von Adlbrecht, Christopher, Aigner, Elmar, Bellón, Juan M., Bouloukaki, Izolde, Bouzas-Mosquera, Alberto, Carrilho, Alexandre J. F., Chang, Kuo-Chu, Chattipakorn, Nipon, Chattipakorn, Siriporn C., Chen, Yi-Jen, Chung, Yuan-Chiang, Colah, Roshan, Datz, Christian, Frøkjær, Jens B., Fujimori, Shunji, Georgiadou, Panagiota, Grion, Cintia M., Hsu, Chih-Ping, Hülsmann, Martin, Hung, Ming-Jui, Hung, Ming-Yow, Iliodromitis, Efstathios K., Lang, Irene M., Lee, Ting- I., März, Winfried, Nair, Sona B., Pascual, Gemma, Peteiro, Jesús, Sakamoto, Choitsu, Satomura, Atsushi, Schiza, Sophia E., Stärkel, Peter, Stojakovic, Tatjana, Vesely, David L., Walters, Darren L., Yilmaz, Yusuf

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Predictors of early neurological deterioration following intravenous thrombolysis: Difference between risk factors for ischemic and hemorrhagic worsening von Nair, Srikumar, Somarajan, Deepthi, Pillai, Rammohan, Balachandran, Keerthi, Sathian, Sona

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Decreasing central line-associated bloodstream infections rates in intensive care units in 30 low- and middle-income countries: An INICC approach von Rosenthal, Victor D., Jin, Zhilin, Brown, Eric C., Dongol, Reshma, De Moros, Daisy A., Alarcon-Rua, Johana, Perez, Valentina, Stagnaro, Juan P., Alkhawaja, Safaa, Jimenez-Alvarez, Luisa F., Cano-Medina, Yuliana A., Valderrama-Beltran, Sandra L., Henao-Rodas, Claudia M., Zuniga-Chavarria, Maria A., El-Kholy, Amani, Agha, Hala, Sahu, Suneeta, Mishra, Shakti B., Bhattacharyya, Mahuya, Kharbanda, Mohit, Poojary, Aruna, Nair, Pravin K., Myatra, Sheila N., Chawla, Rajesh, Sandhu, Kavita, Mehta, Yatin, Rajhans, Prasad, Abdellatif-Daboor, Mohammad, Chian-Wern, Tai, Gan, Chin Seng, Mohd-Basri, Mat Nor, Aguirre-Avalos, Guadalupe, Hernandez-Chena, Blanca E., Sassoe-Gonzalez, Alejandro, Villegas-Mota, Isabel, Aleman- Bocanegra, Mary C., Bat-Erdene, Ider, Carreazo, Nilton Y., Castaneda-Sabogal, Alex, Janc, Jarosław, Hlinkova, Sona, Yildizdas, Dincer, Havan, Merve, Koker, Alper, Sungurtekin, Hulya, Dinleyici, Ener C., Guclu, Ertugrul, Tao, Lili, Memish, Ziad A., Yin, Ruijie

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Waste paper as a viable sustainable source for cellulosic extraction by chlorine free bleaching and acid hydrolysis method for the production of PVA-starch/cellulose based biocompo... von Mohammed Irfan, T.N., Sunitha George, Tresa, Sainul Abidh, K.M., Prakash, Sona, Parambath Kanoth, Bipinbal, George, Neena, Balachandrakurup, Venugopal, Midhun Dominic, C.D., Nair, Ajalesh B

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Glanzmann's thrombasthenia: updated von Nair, Sona, Ghosh, Kanjaksha, Kulkarni, Bipin, Shetty, Shrimati, Mohanty, Dipika

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Hemoglobin Fontainebleau [a21(B2)Ala>Pro]: The second report from India von Mashon, Ranjeet, Nair, Sona, Sawant, Pratibha, Colah, Roshan, Ghosh, Kanjaksha, Das, Sheila

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Human platelet alloantigen polymorphism in Glanzmann's thrombasthenia and its impact on the severity of the disease von Ghosh, Kanjaksha, Kulkarni, Bipin, Nair, Sona, Shetty, Shrimati, Mohanty, Dipika

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Two New β3 Integrin Mutations in Indian Patients with Glanzmann Thrombasthenia: Localization of Mutations Affecting Cysteine Residues in Integrin β3 von NAIR, Sona, JIHONG LI, MITCHELL, W. Beau, MOHANTY, Dipika, COLLER, Barry S, FRENCH, Deborah L

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SRY sequence in maternal plasma: Implications for non-invasive prenatal diagnosis: First report from India von D'Souza, Edna, Nair, Sona, Nadkarni, Anita, Ghosh, Kanjaksha, Colah, Roshan B

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