Arenas J - Search Results

1

Lack of gastrointestinal symptoms in a 60-year-old patient with MNGIE.

Martín MA, Blázquez A, Martí R, Bautista J, Lara MC, Cabello A, Campos Y, Belda O, Andreu AL, Arenas J. Martín MA, et al. Among authors: arenas j. Neurology. 2004 Oct 26;63(8):1536-7. doi: 10.1212/01.wnl.0000141857.37073.97. Neurology. 2004. PMID: 15505189 No abstract available.

2

Respiratory chain enzymes in muscle of endurance athletes: effect of L-carnitine.

Huertas R, Campos Y, Díaz E, Esteban J, Vechietti L, Montanari G, D'Iddio S, Corsi M, Arenas J. Huertas R, et al. Among authors: arenas j. Biochem Biophys Res Commun. 1992 Oct 15;188(1):102-7. doi: 10.1016/0006-291x(92)92355-2. Biochem Biophys Res Commun. 1992. PMID: 1329742 Clinical Trial.

3

Oculopharyngeal muscular dystrophy and mitochondrial abnormalities.

Arenas J, Huertas RA, Campos Y, Cabello A, Gutierrez E, Bautista J, Segura D. Arenas J, et al. Muscle Nerve. 1992 Sep;15(9):1055-6. doi: 10.1002/mus.880150911. Muscle Nerve. 1992. PMID: 1518515 No abstract available.

4

[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: arenas j. Neurologia. 1991 May;6(5):185-7. Neurologia. 1991. PMID: 1908255 Spanish.

5

Mitochondrial DNA deletion in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes (MELAS) and Fanconi's syndrome.

Campos Y, Garcia-Silva T, Barrionuevo CR, Cabello A, Muley R, Arenas J. Campos Y, et al. Among authors: arenas j. Pediatr Neurol. 1995 Jul;13(1):69-72. doi: 10.1016/0887-8994(95)00082-q. Pediatr Neurol. 1995. PMID: 7575854

6

Respiratory chain enzyme defects in patients with idiopathic inflammatory myopathy.

Campos Y, Arenas J, Cabello A, Gomez-Reino JJ. Campos Y, et al. Among authors: arenas j. Ann Rheum Dis. 1995 Jun;54(6):491-3. doi: 10.1136/ard.54.6.491. Ann Rheum Dis. 1995. PMID: 7632092 Free PMC article.

7

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. Among authors: arenas j. Acta Neurol Scand. 1995 Jan;91(1):62-5. doi: 10.1111/j.1600-0404.1995.tb05845.x. Acta Neurol Scand. 1995. PMID: 7732778

8

[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: arenas j. Neurologia. 1994 Oct;9(8):324-36. Neurologia. 1994. PMID: 7803049 Spanish.

9

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. Among authors: arenas j. J Inherit Metab Dis. 1994;17(5):634-5. doi: 10.1007/BF00711608. J Inherit Metab Dis. 1994. PMID: 7837776 No abstract available.

10

Benign mitochondrial myopathy with decreased succinate cytochrome C reductase activity.

Arpa J, Campos Y, Gutiérrez-Molina M, Cruz-Martínez A, Arenas J, Caminero AB, Palomo F, Morales C, Barreiro P. Arpa J, et al. Among authors: arenas j. Acta Neurol Scand. 1994 Oct;90(4):281-4. doi: 10.1111/j.1600-0404.1994.tb02722.x. Acta Neurol Scand. 1994. PMID: 7839816

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