MARÍA TERESA
GARCÍA SILVA
Investigadora hasta 2019
Yolanda
Campos Martín
Publicaciones en las que colabora con Yolanda Campos Martín (7)
2012
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Clinical and cellular consequences of the mutation m.12300G>A in the mitochondrial tRNA Leu(CUN) gene
Mitochondrion, Vol. 12, Núm. 2, pp. 288-293
2005
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Renal pathology in children with mitochondrial diseases
Pediatric Nephrology, Vol. 20, Núm. 9, pp. 1299-1305
1999
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Slow segregation and rapid shift to homoplasmy coexist in a family with the T8993 > G mutation
Journal of Inherited Metabolic Disease, Vol. 22, Núm. 8, pp. 939-940
1998
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Clinical heterogeneity associated with mitochondrial DNA depletion in muscle
Neuromuscular Disorders, Vol. 8, Núm. 8, pp. 568-573
1997
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Syndrome of encephalopathy, petechiae, and ethylmalonic aciduria
Pediatric Neurology, Vol. 17, Núm. 2, pp. 165-170
1995
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Mitochondrial DNA deletion in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes (MELAS) and Fanconi's syndrome
Pediatric Neurology, Vol. 13, Núm. 1, pp. 69-72