Benitez J - Search Results

1

Genetic and epigenetic profile of sporadic pheochromocytomas.

Cascon A, Ruiz-Llorente S, Fraga MF, Leton R, Telleria D, Sastre J, Diez JJ, Martinez Diaz-Guerra G, Diaz Perez JA, Benitez J, Esteller M, Robledo M. Cascon A, et al. Among authors: benitez j. J Med Genet. 2004 Mar;41(3):e30. doi: 10.1136/jmg.2003.012658. J Med Genet. 2004. PMID: 14985401 Free PMC article. No abstract available.

2

SDHB mutation analysis in familial and sporadic phaeochromocytoma identifies a novel mutation.

Cascón A, Cebrián A, Ruiz-Llorente S, Tellería D, Benítez J, Robledo M. Cascón A, et al. Among authors: benitez j. J Med Genet. 2002 Oct;39(10):E64. doi: 10.1136/jmg.39.10.e64. J Med Genet. 2002. PMID: 12362046 Free PMC article. No abstract available.

3

Mutational and gross deletion study of the MEN1 gene and correlation with clinical features in Spanish patients.

Cebrián A, Ruiz-Llorente S, Cascón A, Pollán M, Díez JJ, Picó A, Tellería D, Benítez J, Robledo M. Cebrián A, et al. Among authors: benitez j. J Med Genet. 2003 May;40(5):e72. doi: 10.1136/jmg.40.5.e72. J Med Genet. 2003. PMID: 12746426 Free PMC article. No abstract available.

4

Clinical and genetic characterization of classical forms of familial adenomatous polyposis: a Spanish population study.

Rivera B, González S, Sánchez-Tomé E, Blanco I, Mercadillo F, Letón R, Benítez J, Robledo M, Capellá G, Urioste M. Rivera B, et al. Among authors: benitez j. Ann Oncol. 2011 Apr;22(4):903-909. doi: 10.1093/annonc/mdq465. Epub 2010 Oct 5. Ann Oncol. 2011. PMID: 20924072 Free article.

5

High prevalence of the C634Y mutation in the RET proto-oncogene in MEN 2A families in Spain.

Sánchez B, Robledo M, Biarnes J, Sáez ME, Volpini V, Benítez J, Navarro E, Ruiz A, Antiñolo G, Borrego S. Sánchez B, et al. Among authors: benitez j. J Med Genet. 1999 Jan;36(1):68-70. J Med Genet. 1999. PMID: 9950371 Free PMC article.

6

Trinucleotide (CAG) repeat expansion in chromosomes of Spanish patients with Huntington's disease.

Benitez J, Fernandez E, Garcia Ruiz P, Robledo M, Ramos C, Yébenes J. Benitez J, et al. Hum Genet. 1994 Nov;94(5):563-4. doi: 10.1007/BF00211028. Hum Genet. 1994. PMID: 7959696

7

Incidence of homogeneously staining regions in non-Hodgkin lymphomas.

Arranz E, Robledo M, Martínez B, Gallego J, Román A, Rivas C, Benítez J. Arranz E, et al. Among authors: benitez j. Cancer Genet Cytogenet. 1996 Mar;87(1):1-3. doi: 10.1016/0165-4608(95)00230-8. Cancer Genet Cytogenet. 1996. PMID: 8646732

8

The 12 base pair duplication/insertion alteration could be a regulatory mutation.

Robledo M, Osorio A, Sentís C, Albertos J, Estevez L, Benítez J. Robledo M, et al. Among authors: benitez j. J Med Genet. 1997 Jul;34(7):592-3. doi: 10.1136/jmg.34.7.592. J Med Genet. 1997. PMID: 9222971 Free PMC article.

9

Genetic and clinical analysis in 10 Spanish patients with multiple endocrine neoplasia type 1.

Cebrián A, Herrera-Pombo JL, Díez JJ, Sánchez-Vilar O, Lara JI, Vázquez C, Picó A, Osorio A, Martínez-Delgado B, Benítez J, Robledo M. Cebrián A, et al. Among authors: benitez j. Eur J Hum Genet. 1999 Jul;7(5):585-9. doi: 10.1038/sj.ejhg.5200336. Eur J Hum Genet. 1999. PMID: 10439966

10

Complex cytogenetic abnormalities including telomeric associations and MEN1 mutation in a pediatric ependymoma.

Urioste M, Martínez-Ramírez A, Cigudosa JC, Colmenero I, Madero L, Robledo M, Martínez-Delgado B, Benítez J. Urioste M, et al. Among authors: benitez j. Cancer Genet Cytogenet. 2002 Oct 15;138(2):107-10. doi: 10.1016/s0165-4608(01)00532-5. Cancer Genet Cytogenet. 2002. PMID: 12505253

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