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Journal of Family Medicine and Primary Care|December 4, 2024
A retrospective study to assess adolescent nutritional deficiencies and the association with post-COVID-19 statusArti Gupta, Pentapati Siva Santosh Kumar, Sai Subhakar Desu, et al.Bioinformation|June 12, 2026
Nutritional status among adolescents in India: A school-based retrospective cohort studyArti Gupta, Praveen Kumar S, Srineetha Paruchuri, et al.The Journal of Gene Medicine|March 3, 2018
A novel mutation in SLC39A14 causing hypermanganesemia associated with infantile onset dystoniaMonica Juneja, Uzma Shamim, Aditi Joshi, et al.Journal of Family Medicine and Primary Care|July 15, 2026
From awareness to action: Millet-based recipe talks improve iron status and reduce anemia severity in Andhra Pradesh womenArti Gupta, Joe Amalan, Sirisha Pulla, et al.Pediatric Nephrology (Berlin, Germany)|January 9, 2023
Variants in complement genes are uncommon in patients with anti-factor H autoantibody-associated atypical hemolytic uremic syndromePriyanka Khandelwal, Aditi Joshi, Aradhana Mathur, et al.Journal of the American Society of Nephrology : JASN|October 25, 2002
Inhibitory smads and tgf-Beta signaling in glomerular cellsMario Schiffer, Lena E Schiffer, Arti Gupta, et al.Journal of Public Health Research|March 13, 2024
Alarming levels of inadequate intake of B group vitamins in tribal lactating women from South IndiaPentapati Siva Santosh Kumar, Arti Gupta, Sai Subhakar Desu, et al.Radiographics : a Review Publication of the Radiological Society of North America, Inc|July 2, 2026
Comprehensive Approach to Prostate Cancer Metastasis Mimics at Prostate-Specific Membrane Antigen PET/CTNiloufar Rafiei Alavi, Arti Gupta, Maryam Rahmani, et al.Drug Safety|August 27, 2022
A Prospective Observational Study on BBV152 Coronavirus Vaccine Use in Adolescents and Comparison with Adults: Interim Results of the First Real-World Safety AnalysisUpinder Kaur, Anju K L, Mayank Chauhan, et al.American Journal of Medical Genetics. Part A|July 7, 2020
An Indian child with Coats plus syndrome due to mutations in STN1Gouri Rao Passi, Uzma Shamim, Surabhi Rathore, et al.Pageof 14