Neumann HP - Search Results

1

RASSF1A promoter region CpG island hypermethylation in phaeochromocytomas and neuroblastoma tumours.

Astuti D, Agathanggelou A, Honorio S, Dallol A, Martinsson T, Kogner P, Cummins C, Neumann HP, Voutilainen R, Dahia P, Eng C, Maher ER, Latif F. Astuti D, et al. Among authors: neumann hp. Oncogene. 2001 Nov 8;20(51):7573-7. doi: 10.1038/sj.onc.1204968. Oncogene. 2001. PMID: 11709729

2

Evaluation of a functional epigenetic approach to identify promoter region methylation in phaeochromocytoma and neuroblastoma.

Margetts CD, Morris M, Astuti D, Gentle DC, Cascon A, McRonald FE, Catchpoole D, Robledo M, Neumann HP, Latif F, Maher ER. Margetts CD, et al. Among authors: neumann hp. Endocr Relat Cancer. 2008 Sep;15(3):777-86. doi: 10.1677/ERC-08-0072. Epub 2008 May 22. Endocr Relat Cancer. 2008. PMID: 18499731 Free PMC article.

3

von Hippel-Lindau disease: a clinical and scientific review.

Maher ER, Neumann HP, Richard S. Maher ER, et al. Among authors: neumann hp. Eur J Hum Genet. 2011 Jun;19(6):617-23. doi: 10.1038/ejhg.2010.175. Epub 2011 Mar 9. Eur J Hum Genet. 2011. PMID: 21386872 Free PMC article. Review.

4

The approach to the patient with paraganglioma.

Neumann HP, Eng C. Neumann HP, et al. J Clin Endocrinol Metab. 2009 Aug;94(8):2677-83. doi: 10.1210/jc.2009-0496. J Clin Endocrinol Metab. 2009. PMID: 19657044 Free PMC article.

5

Genetic stratification of inherited and sporadic phaeochromocytoma and paraganglioma: implications for precision medicine.

Casey R, Neumann HPH, Maher ER. Casey R, et al. Among authors: neumann hph. Hum Mol Genet. 2020 Oct 20;29(R2):R128-R137. doi: 10.1093/hmg/ddaa201. Hum Mol Genet. 2020. PMID: 33059362 Free PMC article. Review.

6

Profiling of somatic mutations in phaeochromocytoma and paraganglioma by targeted next generation sequencing analysis.

Luchetti A, Walsh D, Rodger F, Clark G, Martin T, Irving R, Sanna M, Yao M, Robledo M, Neumann HP, Woodward ER, Latif F, Abbs S, Martin H, Maher ER. Luchetti A, et al. Among authors: neumann hp. Int J Endocrinol. 2015;2015:138573. doi: 10.1155/2015/138573. Epub 2015 Mar 25. Int J Endocrinol. 2015. PMID: 25883647 Free PMC article.

7

Consequences of direct genetic testing for germline mutations in the clinical management of families with multiple endocrine neoplasia, type II.

Neumann HP, Eng C, Mulligan LM, Glavac D, Zäuner I, Ponder BA, Crossey PA, Maher ER, Brauch H. Neumann HP, et al. JAMA. 1995 Oct 11;274(14):1149-51. JAMA. 1995. PMID: 7563486

8

Pheochromocytoma and Paraganglioma.

Neumann HPH, Young WF Jr, Eng C. Neumann HPH, et al. N Engl J Med. 2019 Aug 8;381(6):552-565. doi: 10.1056/NEJMra1806651. N Engl J Med. 2019. PMID: 31390501 Review. No abstract available.

9

Pheochromocytoma and Paraganglioma. Reply.

Neumann HPH, Young WF Jr, Eng C. Neumann HPH, et al. N Engl J Med. 2019 Nov 7;381(19):1883. doi: 10.1056/NEJMc1912022. N Engl J Med. 2019. PMID: 31693823 No abstract available.

10

Differential genetic alterations in von Hippel-Lindau syndrome-associated and sporadic pheochromocytomas.

Bender BU, Gutsche M, Gläsker S, Müller B, Kirste G, Eng C, Neumann HP. Bender BU, et al. Among authors: neumann hp. J Clin Endocrinol Metab. 2000 Dec;85(12):4568-74. doi: 10.1210/jcem.85.12.7015. J Clin Endocrinol Metab. 2000. PMID: 11134110 Clinical Trial.

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