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Enfermedades mitocondriales - Asociación Española para el ...

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<strong>Enfermedades</strong> <strong>mitocondriales</strong><br />

solucionan <strong>el</strong> defecto, sino que tratan de corregir parcialmente<br />

<strong>el</strong> defecto bioquímico subyacente. Es importante<br />

monitorizar las concentraciones de los fármacos<br />

aplicados en la terapia, no sólo <strong>para</strong> prevenir los efectos<br />

secundarios que se pudieran desencadenar, sino también<br />

<strong>para</strong> conocer mejor la r<strong>el</strong>ación dosis d<strong>el</strong> fármacoefecto<br />

terapéutico.<br />

Referencias<br />

1. Bernier FP, Boneh A, Dennett X, Chow CW, Cleary MA,<br />

Thorburn DR. Diagnostic criteria for respiratory chain<br />

disorders in adults and children. Neurology 2002; 59: 1406-<br />

1411.<br />

2. Artuch R, Pineda M, Vilaseca MA, Briones P, Ribes A,<br />

Colomer J, Vernet A, Campistol J. Respiratory chain and<br />

pyruvate metabolism deficiencies in pediatric patients:<br />

evaluation of biochemical tests for s<strong>el</strong>ective screening.<br />

Rev Neurol. 1998; 26(149):38-42.<br />

3. Eng<strong>el</strong> WK, Cunningham GC. Rapid examination of muscle<br />

tissue: An improved trichrome stain method for fresh<br />

frozen biopsy sections. Neurology 1963; 13:919-26.<br />

4. Campos Y, Arenas J, Cab<strong>el</strong>lo A, et al. Respiratory chain<br />

enzyme defects in patients with idiopathic inflammatory<br />

myopathy. Ann Rheum Dis 1995b; 54:491-93.<br />

5. González-Crespo R, Arenas J, Gómez-Reino J, et al. Muscle<br />

dysfunction in ederly individuals with hip fracture. J<br />

Rheumatol 1999; 26:2229-32.<br />

6. Holt IJ, Harding AE, Petty RK, et al. A new mitochondrial<br />

disease associated with mitochondrial DNA heteroplasmy.<br />

Am J Hum Genet 1990 ; 46:428-33.<br />

7. Cab<strong>el</strong>lo A, Navarro C, Ricoy JR. Alteraciones morfológicas<br />

de las miopatías <strong>mitocondriales</strong>. Rev Neurol<br />

1998; 26:44-9.<br />

8. Bonilla E, Sciacco M, Tanji K, et al. New morphological<br />

approaches to the study of mitochondrial encephalomyopathies.<br />

Brain Pathol 1992; 2:113-19.<br />

9. DiMauro S, Nicholson JF, Hays AP, et al. Benign infantile<br />

micochondrial myopathy due to reversible cytochrome c<br />

oxidase deficiency. Ann Neurol 1983; 14:226-34.<br />

10. Tritschler HJ, Andreetta F, Moraes CT, et al. Mitochondrial<br />

myopathy of childhood associated with depletion of mitochondrial<br />

DNA. Neurology 1992; 42:209-17.<br />

422

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