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Current global vitamin and cofactor prescribing practices for primary mitochondrial diseases: Results of a European reference network survey.
J Inherit Metab Dis. 2024 Nov 11. doi: 10.1002/jimd.12805. Online ahead of print.
J Inherit Metab Dis. 2024.
PMID: 39529390
Phenotyping mitochondrial glutamyl-tRNA synthetase deficiency (EARS2): A case series and systematic literature review.
Pelayo G, Paiva Coelho M, Correia J, Bandeira A, Nogueira C, Vilarinho L, Martins E.
Pelayo G, et al. Among authors: paiva coelho m.
Neurobiol Dis. 2024 Oct 1;200:106644. doi: 10.1016/j.nbd.2024.106644. Epub 2024 Aug 22.
Neurobiol Dis. 2024.
PMID: 39173847
Free article.
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Management of infantile hemangiomas-experience of a tertiary hospital.
Gomes R, Salazar L, Fraga C, Correia MR, Barbosa-Sequeira J, Fernandes A, Álvares S, Banquart Leitão J, Paiva Coelho M.
Gomes R, et al. Among authors: paiva coelho m.
Eur J Pediatr. 2023 Apr;182(4):1611-1618. doi: 10.1007/s00431-023-04827-2. Epub 2023 Jan 27.
Eur J Pediatr. 2023.
PMID: 36705724
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Diagnosis, management, and follow-up of mitochondrial disorders in childhood: a personalized medicine in the new era of genome sequence.
Paiva Coelho M, Martins E, Vilarinho L.
Paiva Coelho M, et al.
Eur J Pediatr. 2019 Jan;178(1):21-32. doi: 10.1007/s00431-018-3292-x. Epub 2018 Dec 7.
Eur J Pediatr. 2019.
PMID: 30535772
Review.
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