Menéndez MJ - Search Results

1

PCR-based study of the presence of Y-chromosome sequences in patients with Ullrich-Turner syndrome.

Coto E, Toral JF, Menéndez MJ, Hernando I, Plasencia A, Benavides A, López-Larrea C. Coto E, et al. Among authors: menendez mj. Am J Med Genet. 1995 Jul 3;57(3):393-6. doi: 10.1002/ajmg.1320570305. Am J Med Genet. 1995. PMID: 7677140

2

DNA microsatellite analysis of families with autosomal dominant polycystic kidney disease types 1 and 2: evaluation of clinical heterogeneity between both forms of the disease.

Coto E, Sanz de Castro S, Aguado S, Alvarez J, Arias M, Menéndez MJ, López-Larrea C. Coto E, et al. Among authors: menendez mj. J Med Genet. 1995 Jun;32(6):442-5. doi: 10.1136/jmg.32.6.442. J Med Genet. 1995. PMID: 7666395 Free PMC article.

3

[Cystic fibrosis in Asturias: an elevated frequency of the delta F508 mutation].

Coto E, Bousoño C, Menéndez MJ, Cue R, Toral JF, Benavides A, Hernando I, Plasencia A, López-Larrea C. Coto E, et al. Among authors: menendez mj. Med Clin (Barc). 1994 Nov 26;103(18):681-3. Med Clin (Barc). 1994. PMID: 7808073 Spanish.

4

A family with a milder form of adult dominant polycystic kidney disease not linked to the PKD1 (16p) or PKD2 (4q) genes.

Ariza M, Alvarez V, Marín R, Aguado S, López-Larrea C, Alvarez J, Menéndez MJ, Coto E. Ariza M, et al. Among authors: menendez mj. J Med Genet. 1997 Jul;34(7):587-9. doi: 10.1136/jmg.34.7.587. J Med Genet. 1997. PMID: 9222969 Free PMC article.

5

Deletion and methylation of the tumour suppressor gene p16/CDKN2 in primary head and neck squamous cell carcinoma.

González MV, Pello MF, López-Larrea C, Suárez C, Menéndez MJ, Coto E. González MV, et al. Among authors: menendez mj. J Clin Pathol. 1997 Jun;50(6):509-12. doi: 10.1136/jcp.50.6.509. J Clin Pathol. 1997. PMID: 9378820 Free PMC article.

6

Factor V Leiden (R506Q) and risk of venous thromboembolism: a case-control study based on the Spanish population.

García-Gala JM, Alvarez V, Pinto CR, Soto I, Urgellés MF, Menéndez MJ, Carracedo C, López-Larrea C, Coto E. García-Gala JM, et al. Among authors: menendez mj. Clin Genet. 1997 Oct;52(4):206-10. doi: 10.1111/j.1399-0004.1997.tb02548.x. Clin Genet. 1997. PMID: 9383024

7

Loss of heterozygosity and mutation analysis of the p16 (9p21) and p53 (17p13) genes in squamous cell carcinoma of the head and neck.

González MV, Pello MF, López-Larrea C, Suárez C, Menéndez MJ, Coto E. González MV, et al. Among authors: menendez mj. Clin Cancer Res. 1995 Sep;1(9):1043-9. Clin Cancer Res. 1995. PMID: 9816078

8

Mutation analysis of the p53, APC, and p16 genes in the Barrett's oesophagus, dysplasia, and adenocarcinoma.

González MV, Artímez ML, Rodrigo L, López-Larrea C, Menéndez MJ, Alvarez V, Pérez R, Fresno MF, Pérez MJ, Sampedro A, Coto E. González MV, et al. Among authors: menendez mj. J Clin Pathol. 1997 Mar;50(3):212-7. doi: 10.1136/jcp.50.3.212. J Clin Pathol. 1997. PMID: 9155671 Free PMC article.

9

A new de novo Notch3 mutation causing CADASIL.

Coto E, Menéndez M, Navarro R, García-Castro M, Alvarez V. Coto E, et al. Eur J Neurol. 2006 Jun;13(6):628-31. doi: 10.1111/j.1468-1331.2006.01337.x. Eur J Neurol. 2006. PMID: 16796587

10

Analysis of the Micro-RNA-133 and PITX3 genes in Parkinson's disease.

de Mena L, Coto E, Cardo LF, Díaz M, Blázquez M, Ribacoba R, Salvador C, Pastor P, Samaranch L, Moris G, Menéndez M, Corao AI, Alvarez V. de Mena L, et al. Am J Med Genet B Neuropsychiatr Genet. 2010 Sep;153B(6):1234-9. doi: 10.1002/ajmg.b.31086. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 20468068

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