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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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Seeing oneself as a data reuser: How subjectification activates the drivers of data reuse in science.
LaFlamme M, Poetz M, Spichtinger D.
LaFlamme M, et al. Among authors: poetz m.
PLoS One. 2022 Aug 18;17(8):e0272153. doi: 10.1371/journal.pone.0272153. eCollection 2022.
PLoS One. 2022.
PMID: 35980953
Free PMC article.
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Immunostaining of gastric leiomyosarcoma for muscle-specific actin.
Shah IA, Somsin A, Poetz MH.
Shah IA, et al. Among authors: poetz mh.
Am J Clin Pathol. 1992 Mar;97(3):436-7. doi: 10.1093/ajcp/97.3.436.
Am J Clin Pathol. 1992.
PMID: 1371904
No abstract available.
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