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Publications by Salvatore DiMauro

CoQ10 Deficiency Diseases in Adults

Mitochondrion
Molecular MedicineCell BiologyMolecular Biology
2007English

A Novel mtDNA Deletion Associated With Primary Adrenal Insufficiency.† 594

Pediatric Research
Child HealthPediatricsPerinatology
1997English

Miopatia Por Deficiência De Succinato-Citocromo-C-Redutase: Possível Defeito No Complexo II Da Cadeia Respiratória

Arquivos de Neuro-Psiquiatria
Biological PsychiatryNeurology
1989English

Muscle Coenzyme Q10 Level in Statin-Related Myopathy

Archives of Neurology
2005English

Association of Mutations in SCO2, a Cytochrome C Oxidase Assembly Gene, With Early Fetal Lethality

Archives of Neurology
2004English

Nerve Conduction Abnormalities in Patients With MELAS and the A3243G Mutation

Archives of Neurology
2006English

Giuseppe Attardi, MD (1923-2008)

Archives of Neurology
2008English

New DGK Gene Mutations in the Hepatocerebral Form of Mitochondrial DNA Depletion Syndrome

Archives of Neurology
2005English

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