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American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|April 30, 2005
Chronic renal failure and proteinuria in adulthood: Fabry disease predominantly affecting the kidneysMarkus Cybulla, Ellen Schaefer, Susanne Wendt, et al.Endocrinology|January 16, 2014
IGFBP2 is neither sufficient nor necessary for the physiological actions of leptin on glucose homeostasis in male ob/ob miceUrsula H Neumann, Sam Chen, Yuen Yi C Tam, et al.Clinical Endocrinology|April 5, 2013
Testing new susceptibility genes in the cohort of apparently sporadic phaeochromocytoma/paraganglioma patients with clinical characteristics of hereditary syndromesMariola Pęczkowska, Aldona Kowalska, Jacek Sygut, et al.Familial Cancer|March 20, 2012
Nephron sparing surgery in von Hippel-Lindau associated renal cell carcinoma; clinicopathological long-term follow-upC A Jilg, Hartmut P H Neumann, S Gläsker, et al.Journal of Clinical Microbiology|July 1, 1992
Ongoing group B Neisseria meningitidis epidemic in São Paulo, Brazil, due to increased prevalence of a single clone of the ET-5 complexC T Sacchi, L L Pessoa, S R Ramos, et al.Die Pharmazie|January 11, 2005
Cytotoxic activity of nepetin, a flavonoid from Eupatorium ballotaefolium HBKG C G Militão, M R J R Albuquerque, O D L Pessoa, et al.Fitoterapia|January 5, 2023
Anti-inflammatory kaurane diterpenoids of Erythroxylum bezerraeLuana San de O Brito, Alison Batista, Flávia Almeida Santos, et al.Journal of Endocrinological Investigation|May 16, 2006
The malignant potential of a succinate dehydrogenase subunit B germline mutationC Fuentes, E Menéndez, J Pineda, et al.Journal of Stroke and Cerebrovascular Diseases : the Official Journal of National Stroke Association|February 26, 2013
Sequence variations in the von Hippel-Lindau tumor suppressor gene in patients with intracranial aneurysmsJan-Helge Klingler, Marie T Krüger, Johannes R Lemke, et al.Human Molecular Genetics|November 24, 2012
Yeast model for evaluating the pathogenic significance of SDHB, SDHC and SDHD mutations in PHEO-PGL syndromeElena Panizza, Tonino Ercolino, Luigi Mori, et al.Pageof 57