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International Journal of Biometeorology|June 13, 2024
Healthy environments for athleTes (HEAT): environmental conditions along a 90 km ultra-marathon event, South AfricaH Havenga, D Gharbi, N Sewry, et al.Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|July 28, 2012
Correlation of the genotype of paragangliomas and pheochromocytomas with their metabolic phenotype on 3,4-dihydroxy-6-18F-fluoro-L-phenylalanin PETH Christian Rischke, Matthias R Benz, Damian Wild, et al.Cancer Research|May 1, 1998
Two North American families with hereditary papillary renal carcinoma and identical novel mutations in the MET proto-oncogeneL Schmidt, K Junker, G Weirich, et al.Diabetes|September 30, 2010
Disruption of hepatic leptin signaling protects mice from age- and diet-related glucose intoleranceFrank K Huynh, Jasna Levi, Heather C Denroche, et al.Endocrine-Related Cancer|February 22, 2012
Biallelic inactivation of the SDHC gene in renal carcinoma associated with paraganglioma syndrome type 3Angelica Malinoc, Maren Sullivan, Thorsten Wiech, et al.Clinical Genetics|August 4, 2016
Simple and rapid characterization of novel large germline deletions in SDHB, SDHC and SDHD-related paragangliomaA S Hoekstra, B van den Ende, X P Julià, et al.The Journal of Clinical Endocrinology and Metabolism|May 27, 2011
Germline mutations of the TMEM127 gene in patients with paraganglioma of head and neck and extraadrenal abdominal sitesHartmut P H Neumann, Maren Sullivan, Aurelia Winter, et al.British Journal of Cancer|October 27, 2004
Investigation of the role of SDHB inactivation in sporadic phaeochromocytoma and neuroblastomaD Astuti, M Morris, C Krona, et al.Endocrine-Related Cancer|May 24, 2008
Evaluation of a functional epigenetic approach to identify promoter region methylation in phaeochromocytoma and neuroblastomaCaroline D E Margetts, Mark Morris, Dewi Astuti, et al.Proceedings of the National Academy of Sciences of the United States of America|April 1, 1991
Genetic flanking markers refine diagnostic criteria and provide insights into the genetics of Von Hippel Lindau diseaseB R Seizinger, D I Smith, M R Filling-Katz, et al.Pageof 43