Cebrian A - Search Results

1

Hypermethylation of P16ink4a and P15ink4b genes as a marker of disease in the follow-up of non-Hodgkin's lymphomas.

Martinez-Delgado B, Richart A, García MJ, Robledo M, Osorio A, Cebrian A, Rivas C, Benitez J. Martinez-Delgado B, et al. Among authors: cebrian a. Br J Haematol. 2000 Apr;109(1):97-103. doi: 10.1046/j.1365-2141.2000.01991.x. Br J Haematol. 2000. PMID: 10848787 Free article.

2

Molecular analysis of the BRCA2 gene in 16 breast/ovarian cancer Spanish families.

Osorio A, Robledo M, Martínez B, Cebrián A, San Román JM, Albertos J, Lobo F, Benítez J. Osorio A, et al. Among authors: cebrian a. Clin Genet. 1998 Aug;54(2):142-7. doi: 10.1111/j.1399-0004.1998.tb03717.x. Clin Genet. 1998. PMID: 9761393

3

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. Eur J Hum Genet. 1999 Jul;7(5):585-9. doi: 10.1038/sj.ejhg.5200336. Eur J Hum Genet. 1999. PMID: 10439966

4

[Identification of a de novo mutation in a patient without von Hippel-Lindau syndrome: clinical and diagnostic implications].

Cebrián A, Ruiz Barnés P, Osorio A, Martínez-Delgado B, Benítez J, Robledo M. Cebrián A, et al. Neurologia. 1999 Aug-Sep;14(7):362-5. Neurologia. 1999. PMID: 10570625 Spanish.

5

A new germline mutation, R600Q, within the coding region of RET proto-oncogene: a rare polymorphism or a MEN 2 causing mutation?

Sáez ME, Ruiz A, Cebrián A, Morales F, Robledo M, Antiñolo G, Borrego S. Sáez ME, et al. Among authors: cebrian a. Hum Mutat. 2000 Jan;15(1):122. doi: 10.1002/(SICI)1098-1004(200001)15:1<122::AID-HUMU41>3.0.CO;2-7. Hum Mutat. 2000. PMID: 10612852 No abstract available.

6

Identification by comparative genomic hybridization of genetic changes involved in tumoral progression of a T-cell non-Hodgkin lymphoma.

Arranz E, Martínez-Delgado B, Richart A, Osorio A, Cebrián A, Robledo M, Rivas C, Benítez J. Arranz E, et al. Among authors: cebrian a. Cancer Genet Cytogenet. 2000 Feb;117(1):41-4. doi: 10.1016/s0165-4608(99)00139-9. Cancer Genet Cytogenet. 2000. PMID: 10700865

7

Molecular analysis of the BRCA1 and BRCA2 genes in 32 breast and/or ovarian cancer Spanish families.

Osorio A, Barroso A, Martínez B, Cebrián A, San Román JM, Lobo F, Robledo M, Benítez J. Osorio A, et al. Among authors: cebrian a. Br J Cancer. 2000 Apr;82(7):1266-70. doi: 10.1054/bjoc.1999.1089. Br J Cancer. 2000. PMID: 10755399 Free PMC article.

8

Identification of novel SDHD mutations in patients with phaeochromocytoma and/or paraganglioma.

Cascon A, Ruiz-Llorente S, Cebrian A, Telleria D, Rivero JC, Diez JJ, Lopez-Ibarra PJ, Jaunsolo MA, Benitez J, Robledo M. Cascon A, et al. Among authors: cebrian a. Eur J Hum Genet. 2002 Aug;10(8):457-61. doi: 10.1038/sj.ejhg.5200829. Eur J Hum Genet. 2002. PMID: 12111639

9

Different incidence and pattern of p15INK4b and p16INK4a promoter region hypermethylation in Hodgkin's and CD30-Positive non-Hodgkin's lymphomas.

García MJ, Martínez-Delgado B, Cebrian A, Martínez A, Benítez J, Rivas C. García MJ, et al. Among authors: cebrian a. Am J Pathol. 2002 Sep;161(3):1007-13. doi: 10.1016/S0002-9440(10)64261-7. Am J Pathol. 2002. PMID: 12213729 Free PMC article.

10

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: cebrian a. 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.

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