Campos Y - Search Results

1

Mitochondrial haplogroups are associated with clinical pattern of AIDS progression in HIV-infected patients.

Guzmán-Fulgencio M, Jiménez JL, García-Álvarez M, Bellón JM, Fernández-Rodriguez A, Campos Y, Rodríguez C, González-Garcia J, Riera M, Viciana P, Muñoz-Fernández MÁ, Resino S. Guzmán-Fulgencio M, et al. Among authors: campos y. J Acquir Immune Defic Syndr. 2013 Jun 1;63(2):178-83. doi: 10.1097/QAI.0b013e3182893f74. J Acquir Immune Defic Syndr. 2013. PMID: 23666137

2

European mitochondrial DNA haplogroups and liver fibrosis in HIV and hepatitis C virus coinfected patients.

García-Álvarez M, Guzmán-Fulgencio M, Berenguer J, Micheloud D, Campos Y, López JC, Cosín J, Miralles P, Alvarez E, Resino S. García-Álvarez M, et al. Among authors: campos y. AIDS. 2011 Aug 24;25(13):1619-926. doi: 10.1097/QAD.0b013e328349820f. AIDS. 2011. PMID: 21673559

3

European mitochondrial DNA haplogroups and metabolic disorders in HIV/HCV-coinfected patients on highly active antiretroviral therapy.

Micheloud D, Berenguer J, Guzmán-Fulgencio M, Campos Y, García-Álvarez M, Catalán P, Cosín J, Miralles P, López JC, Resino S. Micheloud D, et al. Among authors: campos y. J Acquir Immune Defic Syndr. 2011 Dec 1;58(4):371-8. doi: 10.1097/QAI.0b013e31822d2629. J Acquir Immune Defic Syndr. 2011. PMID: 21792063

4

European mitochondrial haplogroups are associated with CD4+ T cell recovery in HIV-infected patients on combination antiretroviral therapy.

Guzmán-Fulgencio M, Berenguer J, Micheloud D, Fernández-Rodríguez A, García-Álvarez M, Jiménez-Sousa MA, Bellón JM, Campos Y, Cosín J, Aldámiz-Echevarría T, Catalán P, López JC, Resino S. Guzmán-Fulgencio M, et al. Among authors: campos y. J Antimicrob Chemother. 2013 Oct;68(10):2349-57. doi: 10.1093/jac/dkt206. Epub 2013 Jun 7. J Antimicrob Chemother. 2013. PMID: 23749950

5

Variable clinical expression associated with the mutation 3243 np of mitochondrial DNA.

Campos Y, Bautista J, Gutierrez-Rivas E, Llabrés J, Lorenzo G, Arenas J. Campos Y, et al. J Inherit Metab Dis. 1994;17(5):634-5. doi: 10.1007/BF00711608. J Inherit Metab Dis. 1994. PMID: 7837776 No abstract available.

6

Clinical heterogeneity associated with mitochondrial DNA depletion in muscle.

Campos Y, Martín MA, García-Silva T, del Hoyo P, Rubio JC, Castro-Gago M, García-Peñas J, Casas J, Cabello A, Ricoy JR, Arenas J. Campos Y, et al. Neuromuscul Disord. 1998 Dec;8(8):568-73. doi: 10.1016/s0960-8966(98)00080-7. Neuromuscul Disord. 1998. PMID: 10093063

7

Clinical and cellular consequences of the mutation m.12300G>A in the mitochondrial tRNA(Leu(CUN)) gene.

Martín-Jiménez R, Martín-Hernández E, Cabello A, García-Silva MT, Arenas J, Campos Y. Martín-Jiménez R, et al. Among authors: campos y. Mitochondrion. 2012 Mar;12(2):288-93. doi: 10.1016/j.mito.2011.10.004. Epub 2011 Nov 7. Mitochondrion. 2012. PMID: 22094595

8

Clinical variability associated with the mutation at nucleotide position 8344 of the mitochondrial DNA.

Campos Y, Martín MA, Vaamonde J, Cabello A, Esteban J, Arenas J. Campos Y, et al. J Inherit Metab Dis. 1996;19(2):119-22. doi: 10.1007/BF01799408. J Inherit Metab Dis. 1996. PMID: 8739944 No abstract available.

9

Prevalence and progression of mitochondrial diseases: a study of 50 patients.

Arpa J, Cruz-Martínez A, Campos Y, Gutiérrez-Molina M, García-Rio F, Pérez-Conde C, Martín MA, Rubio JC, Del Hoyo P, Arpa-Fernández A, Arenas J. Arpa J, et al. Among authors: campos y. Muscle Nerve. 2003 Dec;28(6):690-5. doi: 10.1002/mus.10507. Muscle Nerve. 2003. PMID: 14639582

10

Leigh syndrome associated with mitochondrial complex I deficiency due to a novel mutation in the NDUFS1 gene.

Martín MA, Blázquez A, Gutierrez-Solana LG, Fernández-Moreira D, Briones P, Andreu AL, Garesse R, Campos Y, Arenas J. Martín MA, et al. Among authors: campos y. Arch Neurol. 2005 Apr;62(4):659-61. doi: 10.1001/archneur.62.4.659. Arch Neurol. 2005. PMID: 15824269

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