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Journal of Pharmacy & Bioallied Sciences|July 14, 2025
Assessment of AI-Driven Software Accuracy in Diagnosing Oral Lesions Using Radiographic ImagingVirendra Singh, Priyesh Mathur, Beena Thakker, et al.Molecular Genetics and Metabolism Reports|July 4, 2024
Estimating prevalence of classical homocystinuria in the United States using Optum's de-identified market clarity dataMahim Jain, Mehul Shah, Kamlesh M Thakker, et al.Brain Research. Molecular Brain Research|May 29, 1998
Gene expression in activated brain microglia: identification of a proteinase inhibitor that increases microglial cell numberS Thakker-Varia, S Elkabes, C Schick, et al.Sensors (Basel, Switzerland)|October 14, 2022
FedMSA: A Model Selection and Adaptation System for Federated LearningRui Sun, Yinhao Li, Tejal Shah, et al.The Journal of Clinical Investigation|March 1, 1997
Idiopathic low molecular weight proteinuria associated with hypercalciuric nephrocalcinosis in Japanese children is due to mutations of the renal chloride channel (CLCN5)S E Lloyd, S H Pearce, W Günther, et al.The Journal of Clinical Endocrinology and Metabolism|September 3, 2009
A missense GATA3 mutation, Thr272Ile, causes the hypoparathyroidism, deafness, and renal dysplasia syndromeKatherine U Gaynor, Irina V Grigorieva, M Andrew Nesbit, et al.Clinical Endocrinology|May 26, 1999
Novel DAX1 mutations in X-linked adrenal hypoplasia congenita and hypogonadotrophic hypogonadismJ H Bassett, D J O'Halloran, G R Williams, et al.European Journal of Cancer (Oxford, England : 1990)|February 14, 2004
Prognostic value of facilitative glucose transporter Glut-1 in oral squamous cell carcinomas treated by surgical resection; results of EORTC Translational Research Fund studiesR J Oliver, R T M Woodwards, P Sloan, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|August 24, 2017
Cinacalcet Rectifies Hypercalcemia in a Patient With Familial Hypocalciuric Hypercalcemia Type 2 (FHH2) Caused by a Germline Loss-of-Function Gα11 MutationCaroline M Gorvin, Fadil M Hannan, Treena Cranston, et al.Endocrine Reviews|November 29, 2020
Multiple Endocrine Neoplasia Type 1: Latest InsightsMaria Luisa Brandi, Sunita K Agarwal, Nancy D Perrier, et al.Pageof 107