Rafael Artuch

Clinical and Molecular Phenotype of Aicardi-Goutières Syndrome

Gillian Rice, Teresa Patrick, Rekha Parmar et al. · The American Journal of Human Genetics · 2007 · 450 citations · Full text

Medicine, Cardiology, Genetics +11

Coenzyme Q deficiency triggers mitochondria degradation by mitophagy

Mario D. Cordero, Leonardo Salviati, Rafael Artuch et al. · Autophagy · 2009 · 192 citations · Full text

Life Sciences, Biochemistry, Cell Biology +17

GDF-15 Is Elevated in Children with Mitochondrial Diseases and Is Induced by Mitochondrial Dysfunction

Raquel Montero, Dèlia Yubero, Joan Villarroya et al. · PLoS ONE · 2016 · 176 citations · Full text

Life Sciences, Biochemistry, Pediatrics +12

Cerebral folate deficiency and leukoencephalopathy caused by a mitochondrial DNA deletion

Merçè Pineda, Aída Ormazábal, Ester López‐Gallardo et al. · Annals of Neurology · 2005 · 158 citations

Life Sciences, Neurology, Neuroscience +17

Total Homocysteine in Pediatric Patients

Marta Vilaseca, Dolores Moyano, Imma Ferrer et al. · Clinical Chemistry · 1997 · 147 citations · Full text

Public Health, Child Health, Pediatrics +12