Teresa L. Campos
Penafiel, Portugal
Last Updated: 09/26/2026
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Found 8 publications
The genetic landscape of mitochondrial diseases in the next-generation sequencing era: a Portuguese cohort study.
Journal: Frontiers in cell and developmental biology
Published: October 31, 2023
How to handle HMG-CoA lyase deficiency and type 1 diabetes? A challenging case report.
Journal: Endocrinologia, diabetes y nutricion
Published: June 07, 2023
Evaluation of Frequency, Clinical Correlation, and Antibodies Confirmation Profile in Patients with Suspected Antiphospholipid Syndrome.
Journal: TH open : companion journal to thrombosis and haemostasis
Published: May 10, 2021
Hyperammonaemic encephalopathy in a teenage girl.
Journal: Journal of paediatrics and child health
Published: May 05, 2021
Phenylketonuria in Portugal: Genotype-phenotype correlations using molecular, biochemical, and haplotypic analyses.
Journal: Molecular genetics & genomic medicine
Published: August 05, 2020
Protocol for the etiological investigation of cerebral palsy
Journal: Revista de neurologia
Published: December 11, 2019
Targeted next generation sequencing identifies novel pathogenic variants and provides molecular diagnoses in a cohort of pediatric and adult patients with unexplained mitochondrial dysfunction.
Journal: Mitochondrion
Published: October 23, 2018
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Last Updated: 09/26/2026