JOAQUÍN
ARENAS BARBERO
Forscher bis um 2007
Hospital Severo Ochoa
Madrid, EspañaPublikationen in Zusammenarbeit mit Forschern von Hospital Severo Ochoa (9)
2005
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Comparative analysis of the pathogenic mechanisms associated with the G8363A and A8296G mutations in the mitochondrial tRNALys gene
Biochemical Journal, Vol. 387, Núm. 3, pp. 773-778
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Mitochondrial respiratory chain diseases. Evaluation and variability in 52 patients
Revista de Neurologia, Vol. 41, Núm. 8, pp. 449-454
2003
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Prevalence and progression of mitochondrial diseases: A study of 50 patients
Muscle and Nerve, Vol. 28, Núm. 6, pp. 690-695
2001
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Mitochondrial dysfunction associated with a mutation in the Notch3 gene in a CADASIL family
Neurology, Vol. 57, Núm. 7, pp. 1235-1238
2000
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Myocardial carnitine and carnitine palmitoyltransferase deficiencies in patients with severe heart failure
Biochimica et Biophysica Acta - Molecular Basis of Disease, Vol. 1502, Núm. 3, pp. 330-336
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The pathogenic role of point mutations affecting the translational initiation codon of mitochondrial genes
Molecular Genetics and Metabolism, Vol. 70, Núm. 3, pp. 238-240
1999
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A double mutation (A8296G and G8363A) in the mitochondrial DNA tRNA(Lys) gene associated with myoclonus epilepsy with ragged-red fibers
Neurology, Vol. 52, Núm. 2, pp. 377-382
1998
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Mitochondrial gene expression and respiratory enzyme activities in cardiac diseases
Biochimica et Biophysica Acta - Molecular Basis of Disease, Vol. 1406, Núm. 1, pp. 85-90
1996
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Mioglobinuria recurrente en una niña, por déficit de carnitín palmitil transferasa
Anales Espanoles de Pediatria, Vol. 44, Núm. 1, pp. 67-69