Publication | Open Access
Imaging Work-Up for Screening of Paraganglioma and Pheochromocytoma in<i>SDHx</i>Mutation Carriers: A Multicenter Prospective Study from the PGL.EVA Investigators
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Citations
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References
2012
Year
In routine practice, the imaging work-up for screening SDHx mutation carriers should include thoraco-abdomino-pelvic computed tomography, head and neck magnetic angiography, and somatostatin receptor scintigraphy. Expert centralized image assessment is recommended.
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2000 | 1.6K | |
Gene Mutations in the Succinate Dehydrogenase Subunit SDHB Cause Susceptibility to Familial Pheochromocytoma and to Familial Paraganglioma Dewi Astuti, Farida Latif, Ashraf Dallol, The American Journal of Human Genetics Somatic VariantFamilial PheochromocytomaGenetic DisorderGeneticsInherited Metabolic Disease | 2001 | 1.1K |
2000 | 878 | |
2005 | 678 | |
2010 | 648 | |
2006 | 566 | |
1983 | 399 | |
2010 | 382 | |
2009 | 370 | |
2009 | 336 |
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