Similar articles for PMID: 10522989

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1979	1
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1995	14
1996	21
1997	19
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2000	8
2001	13
2002	7
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2004	4
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2007	1
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2024	0

1

A novel case of multiple endocrine neoplasia type 2A associated with two de novo mutations of the RET protooncogene.

Tessitore A, Sinisi AA, Pasquali D, Cardone M, Vitale D, Bellastella A, Colantuoni V. Tessitore A, et al. J Clin Endocrinol Metab. 1999 Oct;84(10):3522-7. doi: 10.1210/jcem.84.10.6056. J Clin Endocrinol Metab. 1999. PMID: 10522989

2

Rudolf-Virchow-Preis 1995. The role of RET proto-oncogene mutation analysis in the diagnosis of multiple endocrine neoplasia type 2 (MEN 2) gene carriers and in the discrimination of sporadic and familial medullary thyroid carcinomas and pheochromocytomas.

Komminoth P. Komminoth P. Verh Dtsch Ges Pathol. 1995;79:L-LV. Verh Dtsch Ges Pathol. 1995. PMID: 8600671

3

A novel Val648Ile substitution in RET protooncogene observed in a Cys634Arg multiple endocrine neoplasia type 2A kindred presenting with an adrenocorticotropin-producing pheochromocytoma.

Nunes AB, Ezabella MC, Pereira AC, Krieger JE, Toledo SP. Nunes AB, et al. J Clin Endocrinol Metab. 2002 Dec;87(12):5658-61. doi: 10.1210/jc.2002-020345. J Clin Endocrinol Metab. 2002. PMID: 12466368

4

Molecular and biochemical screening for the diagnosis and management of medullary thyroid carcinoma in multiple endocrine neoplasia type 2A.

Vieira AE, Mello MP, Elias LL, Lau IF, Maciel LM, Moreira AC, Castro M. Vieira AE, et al. Horm Metab Res. 2002 Apr;34(4):202-6. doi: 10.1055/s-2002-26712. Horm Metab Res. 2002. PMID: 11987030

5

The RET protooncogene in sporadic pheochromocytomas: frequent MEN 2-like mutations and new molecular defects.

Beldjord C, Desclaux-Arramond F, Raffin-Sanson M, Corvol JC, De Keyzer Y, Luton JP, Plouin PF, Bertagna X. Beldjord C, et al. J Clin Endocrinol Metab. 1995 Jul;80(7):2063-8. doi: 10.1210/jcem.80.7.7608256. J Clin Endocrinol Metab. 1995. PMID: 7608256

6

Mutations of the ret protooncogene in German multiple endocrine neoplasia families: relation between genotype and phenotype. German Medullary Thyroid Carcinoma Study Group.

Frank-Raue K, Höppner W, Frilling A, Kotzerke J, Dralle H, Haase R, Mann K, Seif F, Kirchner R, Rendl J, Deckart HF, Ritter MM, Hampel R, Klempa J, Scholz GH, Raue F. Frank-Raue K, et al. J Clin Endocrinol Metab. 1996 May;81(5):1780-3. doi: 10.1210/jcem.81.5.8626834. J Clin Endocrinol Metab. 1996. PMID: 8626834

7

Multiple endocrine neoplasia type 2A. Study of a family.

Correia MJ, Lopes LO, Bugalho MJ, Cristina L, Santos AI, Bordalo AD, Pinho B, da Silva HL, Gonçalves MD, Ribeiro C, Tuna JL. Correia MJ, et al. Rev Port Cardiol. 2000 Jan;19(1):11-31. Rev Port Cardiol. 2000. PMID: 10731788 Review. English, Portuguese.

8

Absence of mutations in the MEN2A region of the ret proto-oncogene in non-MEN 2A phaeochromocytomas.

Chew SL, Lavender P, Jain A, Weber A, Ross RJ, Wass JA, Besser GM, Clark AJ. Chew SL, et al. Clin Endocrinol (Oxf). 1995 Jan;42(1):17-21. doi: 10.1111/j.1365-2265.1995.tb02593.x. Clin Endocrinol (Oxf). 1995. PMID: 7889627

9

A new hot spot for mutations in the ret protooncogene causing familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2A.

Berndt I, Reuter M, Saller B, Frank-Raue K, Groth P, Grussendorf M, Raue F, Ritter MM, Höppner W. Berndt I, et al. J Clin Endocrinol Metab. 1998 Mar;83(3):770-4. doi: 10.1210/jcem.83.3.4619. J Clin Endocrinol Metab. 1998. PMID: 9506724

10

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

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