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Journal of Neuromuscular Diseases|December 18, 2023
A Novel Mutation in Frabin (FGD4) Causing a Mild Phenotype of CMT4H in an Indian PatientVikas Nishadham, Rashmi Santhoshkumar, Saraswati Nashi, et al.
Annals of Indian Academy of Neurology|August 8, 2022
Cross-Sectional Area Reference Values of Nerves in the Upper and Lower Extremities using Ultrasonography in the Indian PopulationD M Sindhu, Akshata Huddar, Jitender Saini, et al.
Nano Letters|November 25, 2010
Tracking of multimodal therapeutic nanocomplexes targeting breast cancer in vivoRizia Bardhan, Wenxue Chen, Marc Bartels, et al.
Environmental Microbiology|October 18, 2016
Oral application of Escherichia coli bacteriophage: safety tests in healthy and diarrheal children from BangladeshShafiqul Alam Sarker, Bernard Berger, Ying Deng, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|February 25, 2021
Recessive VAMP1 mutations associated with severe congenital myasthenic syndromes - A recognizable clinical phenotypeKiran Polavarapu, Seena Vengalil, Veeramani Preethish-Kumar, et al.
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