Balmaña J - Search Results

1

Opportunistic testing of BRCA1, BRCA2 and mismatch repair genes improves the yield of phenotype driven hereditary cancer gene panels.

Feliubadaló L, López-Fernández A, Pineda M, Díez O, Del Valle J, Gutiérrez-Enríquez S, Teulé A, González S, Stjepanovic N, Salinas M, Capellá G, Brunet J, Lázaro C, Balmaña J; Catalan Hereditary Cancer Group. Feliubadaló L, et al. Among authors: balmana j. Int J Cancer. 2019 Nov 15;145(10):2682-2691. doi: 10.1002/ijc.32304. Epub 2019 Apr 15. Int J Cancer. 2019. PMID: 30927264 Free article.

2

[Identification of 2 families with hereditary nonpolyposis colonic cancer (HNPCC) and the Amsterdam criteria. Relevance of the genealogic tree and follow-up].

Balmaña J, Brunet J, Capellà G, González D, Palicio M, Sancho FJ, Pericay C, López López JJ, Marcuello E. Balmaña J, et al. Med Clin (Barc). 2000 Jan 22;114(2):56-9. doi: 10.1016/s0025-7753(00)71189-4. Med Clin (Barc). 2000. PMID: 10702951 Spanish.

3

[Clinical and pathological characteristics and clinical course of patients with breast cancer and BRCA1/BRCA2 mutations].

Pericay C, Díez O, Campos B, Balmaña J, Domènech M, Lerma E, Baena M, Maria Sabaté J, Gómez A, José López J, Baiget M, Alonso C. Pericay C, et al. Among authors: balmana j. Med Clin (Barc). 2001 Jul 7;117(5):161-6. doi: 10.1016/s0025-7753(01)72050-7. Med Clin (Barc). 2001. PMID: 11481082 Spanish.

4

BRCA2 mutation analysis of 87 Spanish breast/ovarian cancer families.

Campos B, Diez O, Domènech M, Baena M, Pericay C, Balmaña J, del Rio E, Sanz J, Alonso C, Baiget M. Campos B, et al. Among authors: balmana j. Ann Oncol. 2001 Dec;12(12):1699-703. doi: 10.1023/a:1013517313008. Ann Oncol. 2001. PMID: 11843247 Free article.

5

Mismatch repair gene analysis in Catalonian families with colorectal cancer.

Palicio M, Balmaña J, González S, Blanco I, Marcuello E, Peinado MA, Julià G, Germà JR, López López JJ, Brunet J, Capellà G. Palicio M, et al. Among authors: balmana j. J Med Genet. 2002 Jun;39(6):E29. doi: 10.1136/jmg.39.6.e29. J Med Genet. 2002. PMID: 12070261 Free PMC article. No abstract available.

6

[Description of a new TP53 gene germline mutation in a family with the Li-Fraumeni syndrome. Genetic counselling to healthy mutation carriers].

Balmaña J, Nomdedéu J, Díez O, Sabaté JM, Balil A, Pericay C, López López JJ, Brunet J, Baiget M, Alonso C. Balmaña J, et al. Med Clin (Barc). 2002 Oct 19;119(13):497-9. doi: 10.1016/s0025-7753(02)73474-x. Med Clin (Barc). 2002. PMID: 12406399 Spanish.

7

Haplotype analysis of the BRCA2 9254delATCAT recurrent mutation in breast/ovarian cancer families from Spain.

Campos B, Díez O, Odefrey F, Domènech M, Moncoutier V, Martínez-Ferrandis JI, Osorio A, Balmaña J, Barroso A, Armengod ME, Benítez J, Alonso C, Stoppa-Lyonnet D, Goldgar D, Baiget M. Campos B, et al. Among authors: balmana j. Hum Mutat. 2003 Apr;21(4):452. doi: 10.1002/humu.9133. Hum Mutat. 2003. PMID: 12655574

8

RNA analysis of eight BRCA1 and BRCA2 unclassified variants identified in breast/ovarian cancer families from Spain.

Campos B, Díez O, Domènech M, Baena M, Balmaña J, Sanz J, Ramírez A, Alonso C, Baiget M. Campos B, et al. Among authors: balmana j. Hum Mutat. 2003 Oct;22(4):337. doi: 10.1002/humu.9176. Hum Mutat. 2003. PMID: 12955719

9

Genetic counseling program in familial breast cancer: analysis of its effectiveness, cost and cost-effectiveness ratio.

Balmaña J, Sanz J, Bonfill X, Casado A, Rué M, Gich I, Díez O, Sabaté JM, Baiget M, Alonso MC. Balmaña J, et al. Int J Cancer. 2004 Nov 20;112(4):647-52. doi: 10.1002/ijc.20458. Int J Cancer. 2004. PMID: 15382046 Free article.

10

[Haplotype of the BRCA2 6857delAA mutation in 4 families with breast/ovarian cancer].

Campos B, Díez O, Alvarez C, Palma L, Domènech M, Balmaña J, Sanz J, Ramírez A, Alonso C, Carvallo P, Baiget M. Campos B, et al. Among authors: balmana j. Med Clin (Barc). 2004 Oct 23;123(14):543-5. doi: 10.1016/s0025-7753(04)74590-x. Med Clin (Barc). 2004. PMID: 15535929 Spanish.

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