about
Limited dCTP availability accounts for mitochondrial DNA depletion in mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)Feeding the deoxyribonucleoside salvage pathway to rescue mitochondrial DNA.The neurobiology of autism spectrum disorders.Spotlight on the relevance of mtDNA in cancer.Comparative analysis of the pathogenic mechanisms associated with the G8363A and A8296G mutations in the mitochondrial tRNA(Lys) gene.Administration of deoxyribonucleosides or inhibition of their catabolism as a pharmacological approach for mitochondrial DNA depletion syndrome.Genetically Confirmed Familial Hypercholesterolemia in Patients With Acute Coronary Syndrome.Genetic Etiology for Alcohol-Induced Cardiac Toxicity.Adverse clinical course and poor prognosis of hypertrophic cardiomyopathy due to mutations in FHL1Mild ocular myopathy associated with a novel mutation in mitochondrial twinkle helicaseAssociation of novel POLG mutations and multiple mitochondrial DNA deletions with variable clinical phenotypes in a Spanish populationPrevalence of wild type ATTR assessed as myocardial uptake in bone scan in the elderly population
P50
Q28477625-A7C2D975-D3ED-4476-9FD6-E584A72EB941Q34354792-94957CE8-F96B-4F7E-B805-6075AB1A3694Q34387811-DD27DEEF-5CBC-4B93-ACB1-56BDA382F6DBQ38990083-269039F7-FC24-48C5-9B53-A7306E5A8FF9Q40489976-A1FBBF0B-B448-4934-A926-B83810BD044DQ43423091-00CDD73D-F49E-4DF7-B613-F6716ACC4235Q47668153-B42B89D8-C0FC-4097-8D87-7ACDC1F9CEBDQ53818418-1EF5EDA7-D30B-4CB9-B52E-CBE2FC48EBB8Q60465664-1756C6AC-240C-408A-A334-F4C4ABF2AF92Q80574512-68F08EC6-9DA1-412C-8E4B-A7329F012C29Q82214372-13932E3E-E1E2-419C-BB71-F000BC405CB6Q89106649-2387E57D-AF6A-4830-B750-A249EA207280
P50
description
investigador
@es
researcher
@en
wetenschapper
@nl
name
Emiliano Gonzalez-Vioque
@en
Emiliano Gonzalez-Vioque
@nl
type
label
Emiliano Gonzalez-Vioque
@en
Emiliano Gonzalez-Vioque
@nl
prefLabel
Emiliano Gonzalez-Vioque
@en
Emiliano Gonzalez-Vioque
@nl
P31
P496
0000-0001-7279-4311