Campos Y - Search Results

1

[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.

2

[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.

3

[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.

4

[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.

5

Mitochondrial disease and stroke.

Martínez-Fernández E, Gil-Peralta A, García-Lozano R, Chinchón I, Aguilera I, Fernández-López O, Arenas J, Campos Y, Bautista J. Martínez-Fernández E, et al. Among authors: campos y. Stroke. 2001 Nov;32(11):2507-10. doi: 10.1161/hs1101.098328. Stroke. 2001. PMID: 11692008

6

[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.

7

[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.

8

A novel missense mutation 15747 T>C in the mitochondrial cytochrome b gene.

Aguilera I, García-Lozano JR, Bautista J, Campos Y, Arenas J, Núñez-Roldán A. Aguilera I, et al. Among authors: campos y. Hum Mutat. 1999 Dec;14(6):545. doi: 10.1002/(SICI)1098-1004(199912)14:6<545::AID-HUMU18>3.0.CO;2-J. Hum Mutat. 1999. PMID: 10571957 No abstract available.

9

Lipomatosis, proximal myopathy, and the mitochondrial 8344 mutation. A lipid storage myopathy?

Muñoz-Málaga A, Bautista J, Salazar JA, Aguilera I, Garcia R, Chinchon I, Segura MD, Campos Y, Arenas J. Muñoz-Málaga A, et al. Among authors: campos y. Muscle Nerve. 2000 Apr;23(4):538-42. doi: 10.1002/(sici)1097-4598(200004)23:4<538::aid-mus12>3.0.co;2-t. Muscle Nerve. 2000. PMID: 10716764

10

[The use of cardiopulmonary exercise test in patients with mitochondrial myopathies].

Fernández J, Montemayor T, Bautista J, Márquez R, Jiménez L, Arenas J, Campos Y, Castillo J. Fernández J, et al. Among authors: campos y. Med Clin (Barc). 2000 Feb 5;114(4):121-7. doi: 10.1016/s0025-7753(00)71216-4. Med Clin (Barc). 2000. PMID: 10734620 Spanish.

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