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Annals of Human Genetics|December 2, 2015
Functional Analysis of a Novel Connexin30 Mutation in a Large Family with Hearing Loss, Pesplanus, Ichthyosis, Cutaneous Nodules, and KeratodermaNishtha Pandey, Dennis F Xavier, Arunima Chatterjee, et al.
Sensors (Basel, Switzerland)|April 26, 2025
Development and Assessment of a Soft Wearable for sEMG-Based Hand Grip Detection and Control of a Virtual EnvironmentLohith Chatragadda, Aiden Fletcher, Sam Zhong, et al.
Journal of Clinical and Experimental Hepatology|May 10, 2022
Quality of Life of Patients with Wilson's Disease and Their FamiliesOjas Unavane, Kritika Tiwari, Aabha Nagral, et al.
Blood|October 16, 2025
Human missense variants in F3 impair the initiation of blood coagulationShabbir A Ansari, Marisa A Brake, Nishtha Pathak, et al.
ERJ Open Research|March 30, 2022
Use of single-inhaler triple therapy in the management of obstructive airway disease: Indian medical experts' reviewRaja Dhar, Deepak Talwar, Sundeep Salvi, et al.
NEJM Evidence|February 6, 2024
Living with Asthma in Low- and Middle-Income Countries in the Six WHO RegionsKevin Mortimer, Serif Kurtulus, Arzu Yorgancıoğlu, et al.
Journal of Family Medicine and Primary Care|April 24, 2023
Association of minimum dietary diversity with anaemia among 6-59 months' children from rural India: An evidence from a cross-sectional studyNishtha Kathuria, Prasanta Bandyopadhyay, Shobhit Srivastava, et al.
World Journal of Surgery|January 13, 2022
Parathyroidectomy Versus Cinacalcet for the Treatment of Secondary Hyperparathyroidism in Hemodialysis PatientsLuis Alvarado, Nishtha Sharma, Roxann Lerma, et al.
Neurology India|February 1, 2022
Endoscopic Third Ventriculostomy - A ReviewYad Ram Yadav, Jitin Bajaj, Shailendra Ratre, et al.
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