Eng C - Search Results

1

Neumann HPH, Young WF Jr, Eng C. Neumann HPH, et al. Among authors: eng c. 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.

2

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. Among authors: eng c. JAMA. 1995 Oct 11;274(14):1149-51. JAMA. 1995. PMID: 7563486

3

Low frequency of germline mutations in the RET proto-oncogene in patients with apparently sporadic medullary thyroid carcinoma.

Eng C, Mulligan LM, Smith DP, Healey CS, Frilling A, Raue F, Neumann HP, Ponder MA, Ponder BA. Eng C, et al. Clin Endocrinol (Oxf). 1995 Jul;43(1):123-7. doi: 10.1111/j.1365-2265.1995.tb01903.x. Clin Endocrinol (Oxf). 1995. PMID: 7641404

4

Monogenetic hypertension and pheochromocytoma.

Neumann HP, Bender B, Zäuner I, Berger DP, Eng C, Brauch H, Zbar B. Neumann HP, et al. Among authors: eng c. Am J Kidney Dis. 1996 Sep;28(3):329-33. doi: 10.1016/s0272-6386(96)90488-6. Am J Kidney Dis. 1996. PMID: 8804229

5

Mutation analysis of glial cell line-derived neurotrophic factor, a ligand for an RET/coreceptor complex, in multiple endocrine neoplasia type 2 and sporadic neuroendocrine tumors.

Marsh DJ, Zheng Z, Arnold A, Andrew SD, Learoyd D, Frilling A, Komminoth P, Neumann HP, Ponder BA, Rollins BJ, Shapiro GI, Robinson BG, Mulligan LM, Eng C. Marsh DJ, et al. Among authors: eng c. J Clin Endocrinol Metab. 1997 Sep;82(9):3025-8. doi: 10.1210/jcem.82.9.4197. J Clin Endocrinol Metab. 1997. PMID: 9284737

6

Inherited pheochromocytoma.

Neumann HP, Bender BU, Januszewicz A, Janetschek G, Eng C. Neumann HP, et al. Among authors: eng c. Adv Nephrol Necker Hosp. 1997;27:361-76. Adv Nephrol Necker Hosp. 1997. PMID: 9408456 Review. No abstract available.

7

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: eng c. 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.

8

Somatic and occult germ-line mutations in SDHD, a mitochondrial complex II gene, in nonfamilial pheochromocytoma.

Gimm O, Armanios M, Dziema H, Neumann HP, Eng C. Gimm O, et al. Among authors: eng c. Cancer Res. 2000 Dec 15;60(24):6822-5. Cancer Res. 2000. PMID: 11156372

9

VHL c.505 T>C mutation confers a high age related penetrance but no increased overall mortality.

Bender BU, Eng C, Olschewski M, Berger DP, Laubenberger J, Altehöfer C, Kirste G, Orszagh M, van Velthoven V, Miosczka H, Schmidt D, Neumann HP. Bender BU, et al. Among authors: eng c. J Med Genet. 2001 Aug;38(8):508-14. doi: 10.1136/jmg.38.8.508. J Med Genet. 2001. PMID: 11483638 Free PMC article.

10

Case 13-2001: genetic testing in pheochromocytoma.

Neumann HP, Reincke M, Eng C. Neumann HP, et al. Among authors: eng c. N Engl J Med. 2001 Aug 16;345(7):547-8. N Engl J Med. 2001. PMID: 11519521 No abstract available.

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