Role of rapid sequence whole-body MRI screening in SDH-associated hereditary paraganglioma families
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A. Shaaban | J. Schiffman | W. Kohlmann | K. Jasperson | A. Kirchhoff | L. Buchmann | A. Gammon | J. Hunt | H. Baskin | Heidi Slack | H. Slack
[1] A. Shaaban,et al. Role of rapid sequence whole-body MRI screening in SDH-associated hereditary paraganglioma families , 2013, Familial Cancer.
[2] J. Hamming,et al. High prevalence of occult paragangliomas in asymptomatic carriers of SDHD and SDHB gene mutations , 2012, European Journal of Human Genetics.
[3] M. Mannelli,et al. Updated and New Perspectives on Diagnosis, Prognosis, and Therapy of Malignant Pheochromocytoma/Paraganglioma , 2012, Journal of oncology.
[4] J. Carrasquillo,et al. Staging and functional characterization of pheochromocytoma and paraganglioma by 18F-fluorodeoxyglucose (18F-FDG) positron emission tomography. , 2012, Journal of the National Cancer Institute.
[5] M. Fassnacht,et al. Long-term Postoperative Follow-up in Patients with Apparently Benign Pheochromocytoma and Paraganglioma , 2012, Hormone and Metabolic Research.
[6] M. Kupferman,et al. A novel SDHB mutation associated with hereditary head and neck paraganglioma , 2011, The Laryngoscope.
[7] J. Schiffman. No child left behind in SDHB testing for paragangliomas and pheochromocytomas. , 2011, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[8] J. Beyene,et al. Biochemical and imaging surveillance in germline TP53 mutation carriers with Li-Fraumeni syndrome: a prospective observational study. , 2011, The Lancet. Oncology.
[9] S. Bornstein,et al. Catecholamine metabolomic and secretory phenotypes in phaeochromocytoma. , 2010, Endocrine-related cancer.
[10] J. Bayley,et al. Recent advances in the genetics of SDH-related paraganglioma and pheochromocytoma , 2010, Familial Cancer.
[11] K. Pacak,et al. SDH-related pheochromocytoma and paraganglioma. , 2010, Best practice & research. Clinical endocrinology & metabolism.
[12] M. Merino,et al. Biochemically silent abdominal paragangliomas in patients with mutations in the succinate dehydrogenase subunit B gene. , 2008, The Journal of clinical endocrinology and metabolism.
[13] D. Marsh,et al. Genetic Testing in Pheochromocytoma‐ and Paraganglioma‐Associated Syndromes , 2006, Annals of the New York Academy of Sciences.
[14] K. Byth,et al. Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromes. , 2006, The Journal of clinical endocrinology and metabolism.
[15] C. Eng,et al. Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations. , 2004, JAMA.
[16] G. Chatellier,et al. Imaging work-up for screening of paraganglioma and pheochromocytoma in SDHx mutation carriers: a multicenter prospective study from the PGL.EVA Investigators. , 2013, The Journal of clinical endocrinology and metabolism.
[17] K. Nathanson,et al. Pheochromocytoma and paraganglioma: understanding the complexities of the genetic background. , 2012, Cancer genetics.
[18] J. Carrasquillo,et al. Comparison of 18F-fluoro-L-DOPA, 18F-fluoro-deoxyglucose, and 18F-fluorodopamine PET and 123I-MIBG scintigraphy in the localization of pheochromocytoma and paraganglioma. , 2009, The Journal of clinical endocrinology and metabolism.
[19] R. DeLellis. Pathology and genetics of tumours of endocrine organs , 2004 .