López-Trascasa M - Search Results

1

C7 deficiency and meningococcal infection susceptibility in two spanish families.

Barroso S, López-Trascasa M, Merino D, Alvarez AJ, Núñez-Roldán A, Sánchez B. Barroso S, et al. Scand J Immunol. 2010 Jul;72(1):38-43. doi: 10.1111/j.1365-3083.2010.02403.x. Scand J Immunol. 2010. PMID: 20591074 Free article.

2

Complement component C7 deficiency in two Spanish families.

Barroso S, Sánchez B, Alvarez AJ, López-Trascasa M, Lanuza A, Luque R, Wichmann I, Núñez-Roldán A. Barroso S, et al. Immunology. 2004 Dec;113(4):518-23. doi: 10.1111/j.1365-2567.2004.01997.x. Immunology. 2004. PMID: 15554930 Free PMC article.

3

Molecular defects of the C7 gene in two patients with complement C7 deficiency.

Barroso S, Rieubland C, José álvarez A, López-Trascasa M, Bart PA, Núñez-Roldán A, Sánchez B. Barroso S, et al. Immunology. 2006 Jun;118(2):257-60. doi: 10.1111/j.1365-2567.2006.02364.x. Immunology. 2006. PMID: 16771861 Free PMC article.

4

Complement component C7 deficiency in a Spanish family.

Vázquez-Bermúdez MF, Barroso S, Walter K, Alvarez AJ, Alarcón A, López-Trascasa M, Wichmann I, Aguilar F, Núñez-Roldán A, Sánchez B. Vázquez-Bermúdez MF, et al. Clin Exp Immunol. 2003 Aug;133(2):240-6. doi: 10.1046/j.1365-2249.2003.02186.x. Clin Exp Immunol. 2003. PMID: 12869030 Free PMC article.

5

Molecular characterization of Complement Factor I deficiency in two Spanish families.

Ponce-Castro IM, González-Rubio C, Delgado-Cerviño EM, Abarrategui-Garrido C, Fontán G, Sánchez-Corral P, López-Trascasa M. Ponce-Castro IM, et al. Mol Immunol. 2008 May;45(10):2764-71. doi: 10.1016/j.molimm.2008.02.008. Epub 2008 Mar 28. Mol Immunol. 2008. PMID: 18374984

6

Molecular characterization of three new mutations causing C5 deficiency in two non-related families.

López-Lera A, Garrido S, de la Cruz RM, Fontán G, López-Trascasa M. López-Lera A, et al. Mol Immunol. 2009 Jul;46(11-12):2340-7. doi: 10.1016/j.molimm.2009.03.026. Epub 2009 May 2. Mol Immunol. 2009. PMID: 19414197

7

C5 complement deficiency in a Spanish family. Molecular characterization of the double mutation responsible for the defect.

Delgado-Cerviño E, Fontán G, López-Trascasa M. Delgado-Cerviño E, et al. Mol Immunol. 2005 Jan;42(1):105-11. doi: 10.1016/j.molimm.2004.06.036. Mol Immunol. 2005. PMID: 15488949

8

Combined total deficiency of C7 and C4B with systemic lupus erythematosus (SLE).

Segurado OG, Arnaiz-Villena AA, Iglesias-Casarrubios P, Martinez-Laso J, Vicario JL, Fontan G, Lopez-Trascasa M. Segurado OG, et al. Clin Exp Immunol. 1992 Mar;87(3):410-4. doi: 10.1111/j.1365-2249.1992.tb03011.x. Clin Exp Immunol. 1992. PMID: 1347491 Free PMC article.

9

First case of homozygous C1 inhibitor deficiency.

Blanch A, Roche O, Urrutia I, Gamboa P, Fontán G, López-Trascasa M. Blanch A, et al. J Allergy Clin Immunol. 2006 Dec;118(6):1330-5. doi: 10.1016/j.jaci.2006.07.035. Epub 2006 Sep 18. J Allergy Clin Immunol. 2006. PMID: 17137866

10

Complement factor I deficiency: a not so rare immune defect: characterization of new mutations and the first large gene deletion.

Alba-Domínguez M, López-Lera A, Garrido S, Nozal P, González-Granado I, Melero J, Soler-Palacín P, Cámara C, López-Trascasa M. Alba-Domínguez M, et al. Orphanet J Rare Dis. 2012 Jun 18;7:42. doi: 10.1186/1750-1172-7-42. Orphanet J Rare Dis. 2012. PMID: 22710145 Free PMC article.

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