Campos Y - Search Results

1

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.

2

Clinical heterogeneity in two pedigrees with the 3243 bp tRNA(Leu(UUR)) mutation of mitochondrial DNA.

Campos Y, Bautista J, Gutiérrez-Rivas E, Chinchón D, Cabello A, Segura D, Arenas J. Campos Y, et al. Acta Neurol Scand. 1995 Jan;91(1):62-5. doi: 10.1111/j.1600-0404.1995.tb05845.x. Acta Neurol Scand. 1995. PMID: 7732778

3

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.

4

Sporadic MERRF/MELAS overlap syndrome associated with the 3243 tRNA(Leu(UUR)) mutation of mitochondrial DNA.

Campos Y, Martin MA, Lorenzo G, Aparicio M, Cabello A, Arenas J. Campos Y, et al. Muscle Nerve. 1996 Feb;19(2):187-90. doi: 10.1002/(SICI)1097-4598(199602)19:2<187::AID-MUS10>3.0.CO;2-S. Muscle Nerve. 1996. PMID: 8559168

5

Multiple deletions of mitochondrial DNA in muscle from a patient with benign progressive external ophthalmoplegia.

Campos Y, Martín MA, Rubio JC, Ricard C, Cabello A, Arenas J. Campos Y, et al. J Inherit Metab Dis. 1996;19(3):366-7. doi: 10.1007/BF01799268. J Inherit Metab Dis. 1996. PMID: 8803781 No abstract available.

6

[Molecular genetics of mitochondrial cytopathologies].

Arenas J, Campos Y, Martín MA. Arenas J, et al. Among authors: campos y. Neurologia. 1995 Dec;10 Suppl 1:44-9. Neurologia. 1995. PMID: 8838558 Review. Spanish.

7

Single large-scale mitochondrial DNA deletion in a patient with mitochondrial myopathy associated with multiple symmetric lipomatosis.

Campos Y, Martín MA, Navarro C, Gordo P, Arenas J. Campos Y, et al. Neurology. 1996 Oct;47(4):1012-4. doi: 10.1212/wnl.47.4.1012. Neurology. 1996. PMID: 8857737

8

Leigh syndrome associated with the T9176C mutation in the ATPase 6 gene of mitochondrial DNA.

Campos Y, Martín MA, Rubio JC, Solana LG, García-Benayas C, Terradas JL, Arenas J. Campos Y, et al. Neurology. 1997 Aug;49(2):595-7. doi: 10.1212/wnl.49.2.595. Neurology. 1997. PMID: 9270604

9

Bilateral striatal necrosis and MELAS associated with a new T3308C mutation in the mitochondrial ND1 gene.

Campos Y, Martín MA, Rubio JC, Gutiérrez del Olmo MC, Cabello A, Arenas J. Campos Y, et al. Biochem Biophys Res Commun. 1997 Sep 18;238(2):323-5. doi: 10.1006/bbrc.1997.7166. Biochem Biophys Res Commun. 1997. PMID: 9299504

10

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

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