Primary Hyperoxaluria Type 1 with Homozygosity for a Double-mutated AGXT Allele in a 2-year-old Child

por Krishnamurthy, S., Kartha, G. B., Venkateswaran, V. S., Prasannakumar, M., Mahadevan, S., Gowda, M., Pelle, A., Giachino, D.
Publicado 2017

Maternal and neonatal characteristics, operative details and outcomes in COVID-19 positive parturients undergoing cesarean sections: A retrospective observational study

por Venkateswaran, V., Parida, R., Khanna, P., Bhoi, D., Singh, A.K., Mathur, P., Sahoo, D., Dass, C., Gupta, A., Aravindan, A., Trikha, A.
Publicado 2022

Clinical Profile of Hyper-IgE Syndrome in India

por Saikia, Biman, Rawat, Amit, Minz, Ranjana W., Suri, Deepti, Pandiarajan, Vignesh, Jindal, Ankur, Sahu, Smrity, Karim, Adil, Desai, Mukesh, Taur, Prasad D., Pandrowala, Ambreen, Gowri, Vijaya, Madkaikar, Manisha, Dalvi, Aparna, Yadav, Reetika Mallik, Lashkari, Harsha Prasada, Raj, Revathi, Uppuluri, Ramya, Swaminathan, Venkateswaran V., Bhattad, Sagar, Cyril, Gladys, Kumar, Harish, Shukla, Anuj, Kalra, Manas, Govindaraj, Geeta, Singh, Surjit
Publicado 2021