Arenas J - Search Results

1

Mitochondrial dysfunction associated with a mutation in the Notch3 gene in a CADASIL family.

de la Peña P, Bornstein B, del Hoyo P, Fernández-Moreno MA, Martín MA, Campos Y, Gómez-Escalonilla C, Molina JA, Cabello A, Arenas J, Garesse R. de la Peña P, et al. Among authors: arenas j. Neurology. 2001 Oct 9;57(7):1235-8. doi: 10.1212/wnl.57.7.1235. Neurology. 2001. PMID: 11591842

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

Plasma levels of nitrates in patients with Parkinson's disease.

Molina JA, Jiménez-Jiménez FJ, Navarro JA, Ruiz E, Arenas J, Cabrera-Valdivia F, Vázquez A, Fernández-Calle P, Ayuso-Peralta L, Rabasa M, et al. Molina JA, et al. Among authors: arenas j. J Neurol Sci. 1994 Dec 1;127(1):87-89. doi: 10.1016/0022-510x(94)90139-2. J Neurol Sci. 1994. PMID: 7699396

8

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

9

[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.

10

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.

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