Primary Renal Paragangliomas and Renal Neoplasia Associated with Pheochromocytoma/Paraganglioma: Analysis of von Hippel–Lindau (VHL), Succinate Dehydrogenase (SDHX) and Transmembrane Protein 127 (TMEM127)-Reference-Cited by-同舟云学术

Primary Renal Paragangliomas and Renal Neoplasia Associated with Pheochromocytoma/Paraganglioma: Analysis of von Hippel–Lindau (VHL), Succinate Dehydrogenase (SDHX) and Transmembrane Protein 127 (TMEM127)

Published:2017-06-23 Issue:3 Volume:28 Page:253-268
ISSN:1046-3976
Container-title:Endocrine Pathology
language:en
Short-container-title:Endocr Pathol

Author:

Gupta Sounak,Zhang Jun,Milosevic Dragana,Mills John R.,Grebe Stefan K.,Smith Steven C.,Erickson Lori A.

Publisher

Springer Science and Business Media LLC

Subject

Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism,Pathology and Forensic Medicine

Link

http://link.springer.com/article/10.1007/s12022-017-9489-0/fulltext.html

Reference61 articles.

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2. Lenders, J.W., et al., Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline. The Journal of clinical endocrinology and metabolism, 2014. 99(6): p. 1915–1942.

3. Chen, Y.B., et al., Hereditary leiomyomatosis and renal cell carcinoma syndrome-associated renal cancer: recognition of the syndrome by pathologic features and the utility of detecting aberrant succination by immunohistochemistry. The American journal of surgical pathology, 2014. 38(5): p. 627–637.

4. Lubensky, I.A., et al., Hereditary and sporadic papillary renal carcinomas with c-met mutations share a distinct morphological phenotype. The American journal of pathology, 1999. 155(2): p. 517–526.

5. Schmidt, L.S. and W.M. Linehan, Molecular genetics and clinical features of Birt-Hogg-Dube syndrome. Nature reviews. Urology, 2015. 12(10): p. 558–569.

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