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Items: 6

1.

[Unusual molecular changes in two families with Friedreich's ataxia].

González MC, Díaz-Golpe V, Hernández L, Martin S, Fernández F.

Neurologia. 2003 Sep;18(7):392-5. Spanish.

PMID:
14505249
2.

Combination of congenital coagulation disorders: Factor II gene mutation G20210A, Factor V Leiden gene mutation G1691A and protein S deficiency. a family study.

González CM, Díaz-Golpe V, Martín S, Sánchez Del Real J, Redondo MC.

Haematologica. 2003 Jun;88(6):ECR20. No abstract available.

3.

[Degree of association between serum levels and genotype in alpha-1-antitrypsin deficiency. Clinical usefulness].

Martín Liras S, Díaz-Golpe V, Rivera Sevane F, González Cocaño M, Olcoz Goñi J, Linares Torres P, Jorquera Plaza F.

Gastroenterol Hepatol. 2001 Dec;24(10):478-82. Spanish.

PMID:
11730615
4.

Impairment of metabolic function in chronic hepatitis C is related to factors associated with resistance to therapy.

Jorquera F, Almar M, Díaz-Golpe V, Olcóz JL, García-Fernández A, González-Gallego J.

Am J Gastroenterol. 2001 Aug;96(8):2456-61.

PMID:
11513190
5.

C282Y and H63D mutations of the haemochromatosis gene in patients with iron overload.

Jorquera F, Domínguez A, Díaz-Golpe V, Espinel J, Muñoz F, Herrera A, Fernández-Gundín MJ, Vivas S, Olcoz JL.

Rev Esp Enferm Dig. 2001 May;93(5):293-302. English, Spanish.

PMID:
11488107
6.

A dominant negative protein kinase C zeta subspecies blocks NF-kappa B activation.

Diaz-Meco MT, Berra E, Municio MM, Sanz L, Lozano J, Dominguez I, Diaz-Golpe V, Lain de Lera MT, Alcamí J, Payá CV, Arenzana-Seisedos F, Virelizier JL, Moscat J, et al.

Mol Cell Biol. 1993 Aug;13(8):4770-5.

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