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Pediatric Pulmonology|May 5, 2016
A multicenter study on the utility and safety of EBUS-TBNA and EUS-B-FNA in childrenSahajal Dhooria, Karan Madan, Vallandramam Pattabhiraman, et al.International Journal of Infectious Diseases : IJID : Official Publication of the International Society for Infectious Diseases|December 12, 2018
Isolation and molecular characterization of dengue virus clinical isolates from pediatric patients in New DelhiMeenakshi Kar, Amul Nisheetha, Anuj Kumar, et al.Clinical Genetics|July 15, 2024
Genetics of 67 patients of suspected primary ciliary dyskinesia from IndiaKana Ram Jat, Mohammed Faruq, Shishir Jindal, et al.Scientific Reports|July 21, 2017
Novel transcriptional signatures for sputum-independent diagnostics of tuberculosis in childrenJohn Espen Gjøen, Synne Jenum, Dhanasekaran Sivakumaran, et al.Optics Express|May 4, 2026
Characterization studies of photonic wire bonding for fiber array integrationMd Omar Faruk Rasel, Yash Kabra, Peng Yao, et al.Journal of Low Temperature Physics|January 20, 2025
The Simons Observatory: Design, Optimization, and Performance of Low-Frequency DetectorsAashrita Mangu, Benjamin Westbrook, Shawn Beckman, et al.JACC. Clinical Electrophysiology|February 19, 2025
Pilot Study of Early Catheter Ablation and Neurological Outcomes in Atrial Fibrillation-Related Stroke: RESCUE-STROKEAashish Katapadi, Jalaj Garg, Nikhila Chelikam, et al.Journal of Precision Medicine (Amsterdam, Netherlands)|July 8, 2026
Precision therapeutic tRNA rescue of nonsense mutation R166X in KCNJ13 to restore K+ channel functionAllison Spillane, Enes Akyuz, Meha Kabra, et al.Nature Communications|March 1, 2016
Hypothalamic leptin action is mediated by histone deacetylase 5Dhiraj G Kabra, Katrin Pfuhlmann, Cristina García-Cáceres, et al.Journal of Medical Genetics|February 7, 2006
Mutations of human TMHS cause recessively inherited non-syndromic hearing lossM I Shabbir, Z M Ahmed, S Y Khan, et al.Pageof 153