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Journal of Pediatric Endocrinology & Metabolism : JPEM|February 3, 2025
Insights in non-CAH pediatric primary adrenal insufficiency: a single-center experience from IndiaAaditya Daga, Manjiri Karlekar, Anurag Lila, et al.Human Molecular Genetics|December 15, 2000
Mice lacking renal chloride channel, CLC-5, are a model for Dent's disease, a nephrolithiasis disorder associated with defective receptor-mediated endocytosisS S Wang, O Devuyst, P J Courtoy, et al.Diabetes Care|June 25, 2010
The effects of fenofibric acid alone and with statins on the prevalence of metabolic syndrome and its diagnostic components in patients with mixed dyslipidemiaHarold E Bays, Eli M Roth, James M McKenney, et al.Current Problems in Cardiology|November 29, 2021
Use of Coronary Intravascular Lithotripsy: A Comprehensive Review of LiteratureDeaa Abu Jazar, Ravi Thakker, Salman Salehin, et al.Gut|October 1, 1993
Non-penetrance and late appearance of polyps in families with familial adenomatous polyposisD G Evans, S P Guy, N Thakker, et al.Clinical Endocrinology|April 12, 2001
Absence of mutations in the growth hormone (GH)-releasing hormone receptor gene in GH-secreting pituitary adenomasR Salvatori, R V Thakker, M B Lopes, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|February 27, 2026
Refractory Hypocalcemia from Combined Autosomal Dominant Hypocalcemia Type 2 and Postsurgical HypoparathyroidismMelda Sonmez Ince, Nazanene H Esfandiari, Fadil M Hannan, et al.Journal of Translational Medicine|August 20, 2025
SC134-deruxtecan, a fucosyl-GM1 targeting ADC for small cell lung cancer therapyBryony Heath, Bubacarr G Kaira, Dhruma Thakker, et al.Drug Metabolism and Disposition: the Biological Fate of Chemicals|December 11, 2012
Compartmental and enzyme kinetic modeling to elucidate the biotransformation pathway of a centrally acting antitrypanosomal prodrugClaudia N Generaux, Garrett R Ainslie, Arlene S Bridges, et al.American Journal of Human Genetics|November 1, 1995
Severe Gardner syndrome in families with mutations restricted to a specific region of the APC geneD R Davies, J G Armstrong, N Thakker, et al.Pageof 107