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Publications by Silvio Ferraris
New DGK Gene Mutations in the Hepatocerebral Form of Mitochondrial DNA Depletion Syndrome
Archives of Neurology
Related publications
Hearing Loss in a Patient With the Myopathic Form of Mitochondrial DNA Depletion Syndrome and a Novel Mutation in the TK2 Gene
Pediatric Research
Child Health
Pediatrics
Perinatology
Mitochondrial DNA Depletion, Mitochondrial Mutations and High TFAM Expression in Hepatocellular Carcinoma
Oncotarget
Oncology
First Cases of MPV17 Related Mitochondrial DNA Depletion Syndrome With Compound Heterozygous Mutations in p.R50Q/p.R50W: A Case Report
Hepatoma Research
Mitochondrial DNA Depletion Syndrome Is Expressed in Amniotic Fluid Cell Cultures
American Journal of Pathology
Forensic Medicine
Pathology
The Prevalence of Mitochondrial DNA Mutations in Leigh Syndrome in a Brazilian Series
Medical Express
Lipopolysaccharide-Induced Mitochondrial DNA Depletion
Antioxidants and Redox Signaling
Cell Biology
Molecular Biology
Biochemistry
Clinical Biochemistry
Medicine
Physiology
The Effect of Mitochondrial DNA Mutations in Brain Tumors
Journal of Basic and Clinical Health Sciences
Four Novel Thymidine Phosphorylase Gene Mutations in Mitochondrial Neurogastrointestinal Encephalomyopathy Syndrome (MNGIE) Patients
European Journal of Human Genetics
Genetics
Depletion of Mitochondrial DNA in Differentiated Retinal Pigment Epithelial Cells
Scientific Reports
Multidisciplinary