Arenas J - Search Results

1

Frequency of the C34T mutation of the AMPD1 gene in world-class endurance athletes: does this mutation impair performance?

Rubio JC, Martín MA, Rabadán M, Gómez-Gallego F, San Juan AF, Alonso JM, Chicharro JL, Pérez M, Arenas J, Lucia A. Rubio JC, et al. Among authors: arenas j. J Appl Physiol (1985). 2005 Jun;98(6):2108-12. doi: 10.1152/japplphysiol.01371.2004. Epub 2005 Jan 27. J Appl Physiol (1985). 2005. PMID: 15677729 Free article. Clinical Trial.

2

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. Among authors: arenas j. 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

3

Respiratory-chain enzyme activities in isolated mitochondria of lymphocytes from untreated Parkinson's disease patients. Grupo-Centro de Trastornos del Movimiento.

Martín MA, Molina JA, Jiménez-Jiménez FJ, Benito-León J, Ortí-Pareja M, Campos Y, Arenas J. Martín MA, et al. Among authors: arenas j. Neurology. 1996 May;46(5):1343-6. doi: 10.1212/wnl.46.5.1343. Neurology. 1996. PMID: 8628479

4

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. Among authors: arenas j. J Inherit Metab Dis. 1996;19(2):119-22. doi: 10.1007/BF01799408. J Inherit Metab Dis. 1996. PMID: 8739944 No abstract available.

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. Among authors: arenas j. 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. 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. Among authors: arenas j. Neurology. 1996 Oct;47(4):1012-4. doi: 10.1212/wnl.47.4.1012. Neurology. 1996. PMID: 8857737

8

Abnormal carnitine distribution in the muscles of patients with idiopathic inflammatory myopathy.

Arenas J, Gonzalez-Crespo MR, Campos Y, Martin MA, Cabello A, Gomez-Reino JJ. Arenas J, et al. Arthritis Rheum. 1996 Nov;39(11):1869-74. doi: 10.1002/art.1780391113. Arthritis Rheum. 1996. PMID: 8912509

9

Respiratory chain enzyme activities in isolated mitochondria of lymphocytes from patients with Alzheimer's disease.

Molina JA, de Bustos F, Jiménez-Jiménez FJ, Benito-León J, Gasalla T, Ortí-Pareja M, Vela L, Bermejo F, Martín MA, Campos Y, Arenas J. Molina JA, et al. Among authors: arenas j. Neurology. 1997 Mar;48(3):636-8. doi: 10.1212/wnl.48.3.636. Neurology. 1997. PMID: 9065539 Clinical Trial.

10

Cerebrospinal fluid carnitine levels in patients with Parkinson's disease.

Jiménez-Jiménez FJ, Rubio JC, Molina JA, Martín MA, Campos Y, Benito-León J, Ortí-Pareja M, Gasalla T, Arenas J. Jiménez-Jiménez FJ, et al. Among authors: arenas j. J Neurol Sci. 1997 Feb 12;145(2):183-5. doi: 10.1016/s0022-510x(96)00259-6. J Neurol Sci. 1997. PMID: 9094047 Clinical Trial.

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