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zajkowska k
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Genetic newborn screening and digital technologies: A project protocol based on a dual approach to shorten the rare diseases diagnostic path in Europe.
PLoS One. 2023 Nov 22;18(11):e0293503. doi: 10.1371/journal.pone.0293503. eCollection 2023.
PLoS One. 2023.
PMID: 37992053
Free PMC article.
Rare diseases' genetic newborn screening as the gateway to future genomic medicine: the Screen4Care EU-IMI project.
Ferlini A, Gross ES, Garnier N; Screen4Care consortium.
Ferlini A, et al.
Orphanet J Rare Dis. 2023 Oct 4;18(1):310. doi: 10.1186/s13023-023-02916-x.
Orphanet J Rare Dis. 2023.
PMID: 37794437
Free PMC article.
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FindZebra online search delving into rare disease case reports using natural language processing.
Liévin V, Hansen JM, Lund A, Elstein D, Matthiesen ME, Elomaa K, Zarakowska K, Himmelhan I, Botha J, Borgeskov H, Winther O.
Liévin V, et al. Among authors: zarakowska k.
PLOS Digit Health. 2023 Jun 29;2(6):e0000269. doi: 10.1371/journal.pdig.0000269. eCollection 2023 Jun.
PLOS Digit Health. 2023.
PMID: 37384616
Free PMC article.
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