Domènech M - Search Results

1

[Frequency of thiopurine S-methyltransferase alleles in different ethnic groups living in Spain].

Corominas H, Domènech M, del Río E, Gich I, Domingo P, Baiget M. Corominas H, et al. Among authors: domenech m. Med Clin (Barc). 2006 Mar 25;126(11):410-2. doi: 10.1157/13086124. Med Clin (Barc). 2006. PMID: 16595084 Spanish.

2

Allelic variants of the thiopurine S-methyltransferase deficiency in patients with ulcerative colitis and in healthy controls.

Corominas H, Domènech M, González D, Diaz C, Roca M, García-González MA, Peña S, Baiget M. Corominas H, et al. Among authors: domenech m. Am J Gastroenterol. 2000 Sep;95(9):2313-7. doi: 10.1111/j.1572-0241.2000.02256.x. Am J Gastroenterol. 2000. PMID: 11007234

3

[Aplasia after azathioprine administration: role of the thiopurine methyltransferase genetic polymorphism].

Corominas H, Domènech M, González-Juan D, González-Suárez B, Díaz C, Pujol J, Vázquez G, Baiget M. Corominas H, et al. Among authors: domenech m. Med Clin (Barc). 2000 Sep 16;115(8):299-301. doi: 10.1016/s0025-7753(00)71540-5. Med Clin (Barc). 2000. PMID: 11093885 Spanish.

4

Is thiopurine methyltransferase genetic polymorphism a major factor for withdrawal of azathioprine in rheumatoid arthritis patients?

Corominas H, Domènech M, Laíz A, Gich I, Geli C, Díaz C, de Cuevillas F, Moreno M, Vázquez G, Baiget M. Corominas H, et al. Among authors: domenech m. Rheumatology (Oxford). 2003 Jan;42(1):40-5. doi: 10.1093/rheumatology/keg028. Rheumatology (Oxford). 2003. PMID: 12509611

5

[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: domenech m. 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.

6

[Mutations in the BRCA1 gene in young Spanish women with breast cancer].

Díez Gibert O, del Río E, Domènech M, Hernández EM, Sanz J, Brunet J, Alonso MC, Baiget M. Díez Gibert O, et al. Among authors: domenech m. Med Clin (Barc). 1999 Jan 23;112(2):51-4. Med Clin (Barc). 1999. PMID: 10065429 Spanish.

7

[The identification of a new mutation in the BRCA2 gene by protein truncation analysis in a Spanish family with hereditary breast cancer].

Díez O, del Río E, Domènech M, Sanz J, Cortés J, Brunet J, Alonso Mdel C, Baiget M. Díez O, et al. Among authors: domenech m. Med Clin (Barc). 1999 Feb 13;112(5):179-81. Med Clin (Barc). 1999. PMID: 10091212 Spanish.

8

The prothrombin 20210A allele influences clinical manifestations of hemophilia A in patients with intron 22 inversion and without inhibitors.

Tizzano EF, Soria JM, Coll I, Guzmán B, Cornet M, Altisent C, Martorell M, Domenech M, del Río E, Fontcuberta J, Baiget M. Tizzano EF, et al. Among authors: domenech m. Haematologica. 2002 Mar;87(3):279-85. Haematologica. 2002. PMID: 11869940

9

Identification of the 185delAG BRCA1 mutation in a Spanish Gypsy population.

Díez O, Doménech M, Alonso MC, Brunet J, Sanz J, Cortés J, del Río E, Baiget M. Díez O, et al. Among authors: domenech m. Hum Genet. 1998 Dec;103(6):707-8. doi: 10.1007/s004390050895. Hum Genet. 1998. PMID: 9921907

10

BRCA1 mutation analysis in 83 Spanish breast and breast/ovarian cancer families.

Díez O, Cortés J, Domènech M, Brunet J, Del Río E, Pericay C, Sanz J, Alonso C, Baiget M. Díez O, et al. Among authors: domenech m. Int J Cancer. 1999 Nov 12;83(4):465-9. doi: 10.1002/(sici)1097-0215(19991112)83:4<465::aid-ijc5>3.0.co;2-4. Int J Cancer. 1999. PMID: 10508480

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