Campos Y - Search Results

1

[Complex I (NADH coenzyme-Q-reductase) deficiency, MELAS syndrome and hypertrophic cardiomyopathy].

Márquez C, Bautista J, Arenas J, Segura D, Chinchón I, Rafel E, Campos Y, Huerta R. Márquez C, et al. Among authors: campos y. Neurologia. 1991 May;6(5):185-7. Neurologia. 1991. PMID: 1908255 Spanish.

2

[Adult onset mitochondrial myopathy without ophthalmoplegia. Four cases attributable to complex III and IV deficits in the respiratory chain].

Bautista J, Muñoz-Málaga A, Chinchón I, Segura D, Salazar JA, Bescansa E, Campos Y, Arenas J. Bautista J, et al. Among authors: campos y. Neurologia. 1995 Oct;10(8):319-23. Neurologia. 1995. PMID: 8554781 Spanish.

3

Myophosphorylase deficiency associated with a defect in complex I of the mitochondrial respiratory chain.

Rubio JC, Martín MA, Bautista J, Campos Y, Segura D, Cabello A, Chinchón I, Arenas J. Rubio JC, et al. Among authors: campos y. J Neurol Sci. 1998 Dec 11;161(2):110-3. doi: 10.1016/s0022-510x(98)00263-9. J Neurol Sci. 1998. PMID: 9879690

4

[Mitochondrial encephalomyopathy of late presentation with progressive ophthalmoplegia, tremor and diffuse leukoencephalopathy].

Franco E, Bautista J, Luque R, Chinchón I, García-Lozano R, Aguilera I, Campos Y, Arenas J. Franco E, et al. Among authors: campos y. Neurologia. 1999 Nov;14(9):463-6. Neurologia. 1999. PMID: 10613022 Spanish.

5

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

6

[Clinical and investigative approaches in mitochondrial diseases. A review of 15 cases].

Arpa J, Campos Y, Cruz Martínez A, Gutiérrez Molina M, Arenas J, Alonso M, Plaza I, Morales C, Palomo F, Barreiro P, et al. Arpa J, et al. Among authors: campos y. Neurologia. 1994 Oct;9(8):324-36. Neurologia. 1994. PMID: 7803049 Spanish.

7

[Complex I and IV deficits in the mitochondrial respiratory chain in two siblings with type I glutaric aciduria].

Martínez Bermejo A, Pascual Castroviejo I, Merinero B, Campos Y, López Martín V, Arcas J, Gutiérrez Molina M, Arenas J. Martínez Bermejo A, et al. Among authors: campos y. Neurologia. 1994 Aug-Sep;9(7):303-6. Neurologia. 1994. PMID: 7946428 Spanish.

8

[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.

9

Association of genetically proven deficiencies of myophosphorylase and AMP deaminase: a second case of 'double trouble'.

Rubio JC, Martín MA, Bautista J, Campos Y, Segura D, Arenas J. Rubio JC, et al. Among authors: campos y. Neuromuscul Disord. 1997 Sep;7(6-7):387-9. doi: 10.1016/s0960-8966(97)00095-3. Neuromuscul Disord. 1997. PMID: 9327403

10

[Molecular genetics of disorders of the mitochondrial respiratory chain].

Campos Y, Martín MA, Arenas J. Campos Y, et al. Rev Neurol. 2002 Jul 16-31;35(2):153-8. Rev Neurol. 2002. PMID: 12221629 Free article. Review. Spanish.

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