Neumann HPH - Search Results

1

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.

2

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

Maher ER, Neumann HP, Richard S. Maher ER, et al. 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.

3

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. Int J Endocrinol. 2015;2015:138573. doi: 10.1155/2015/138573. Epub 2015 Mar 25. Int J Endocrinol. 2015. PMID: 25883647 Free PMC article.

4

Maternal and fetal outcomes in phaeochromocytoma and pregnancy: a multicentre retrospective cohort study and systematic review of literature.

Bancos I, Atkinson E, Eng C, Young WF Jr, Neumann HPH; International Pheochromocytoma and Pregnancy Study Group. Bancos I, et al. Among authors: neumann hph. Lancet Diabetes Endocrinol. 2021 Jan;9(1):13-21. doi: 10.1016/S2213-8587(20)30363-6. Epub 2020 Nov 26. Lancet Diabetes Endocrinol. 2021. PMID: 33248478 Free PMC article.

5

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. 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.

6

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

7

Characterization of endolymphatic sac tumors and von Hippel-Lindau disease in the International Endolymphatic Sac Tumor Registry.

Bausch B, Wellner U, Peyre M, Boedeker CC, Hes FJ, Anglani M, de Campos JM, Kanno H, Maher ER, Krauss T, Sansó G, Barontini M, Letizia C, Hader C, Schiavi F, Zanoletti E, Suárez C, Offergeld C, Malinoc A, Zschiedrich S, Glasker S, Bobin S, Sterkers O, Ba Huy PT, Giraud S, Links T, Eng C, Opocher G, Richard S, Neumann HP; International Endolymphatic Sac Tumor (ELST) Consortium. Bausch B, et al. Head Neck. 2016 Apr;38 Suppl 1:E673-9. doi: 10.1002/hed.24067. Epub 2015 Jul 14. Head Neck. 2016. PMID: 25867206

8

Variant type is associated with disease characteristics in SDHB, SDHC and SDHD-linked phaeochromocytoma-paraganglioma.

Bayley JP, Bausch B, Rijken JA, van Hulsteijn LT, Jansen JC, Ascher D, Pires DEV, Hes FJ, Hensen EF, Corssmit EPM, Devilee P, Neumann HPH. Bayley JP, et al. Among authors: neumann hph. J Med Genet. 2020 Feb;57(2):96-103. doi: 10.1136/jmedgenet-2019-106214. Epub 2019 Sep 6. J Med Genet. 2020. PMID: 31492822

9

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. Oncogene. 2001 Nov 8;20(51):7573-7. doi: 10.1038/sj.onc.1204968. Oncogene. 2001. PMID: 11709729

10

When should genetic testing be obtained in a patient with phaeochromocytoma or paraganglioma?

Erlic Z, Neumann HP. Erlic Z, et al. Clin Endocrinol (Oxf). 2009 Mar;70(3):354-7. doi: 10.1111/j.1365-2265.2008.03480.x. Epub 2008 Dec 3. Clin Endocrinol (Oxf). 2009. PMID: 19067729

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