C. Pereira
发表
A. Tessa,
F. Santorelli,
L. Vilarinho,
2011,
Genetics research international.
E. Martins,
E. Rodrigues,
L. Vilarinho,
2019,
Mitochondrion.
L. Vilarinho,
L. Vedolin,
F. Vairo,
2019,
Journal of Inborn Errors of Metabolism and Screening.
L. Vilarinho,
A. Guimarães,
L. Almeida,
2017,
Muscle & nerve.
L. Vilarinho,
Liliana Igreja,
D. Quelhas,
2023,
Parkinsonism & related disorders.
Identification of a new mtDNA mutation (14724G>A) associated with mitochondrial leukoencephalopathy.
A. Tessa,
F. Santorelli,
L. Vilarinho,
2007,
Biochemical and biophysical research communications.
E. Martins,
E. Rodrigues,
L. Vilarinho,
2023,
Genes.
mtDNA single macrodeletions associated with myopathies: Absence of haplogroup-related increased risk
A. Amorim,
L. Vilarinho,
L. Pereira,
2005,
Journal of Inherited Metabolic Disease.