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Year | Number of Results |
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2015 | 1 |
2017 | 1 |
2018 | 1 |
2020 | 2 |
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2024 | 1 |
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[Identification and transfer movements among caregivers in neonatal and pediatric intensive care].
Soins Pediatr Pueric. 2023 Jul-Aug;44(333):19-23. doi: 10.1016/j.spp.2023.06.007. Epub 2023 Jul 27.
Soins Pediatr Pueric. 2023.
PMID: 37574228
French.
Effect of brincidofovir on adenovirus and A549 cells transcriptome profiles.
Salmona M, Feghoul L, Mercier-Delarue S, Diaz E, Splitberger M, Armero A, Dalle JH, Dutrieux J, LeGoff J.
Salmona M, et al.
Antiviral Res. 2020 Oct;182:104872. doi: 10.1016/j.antiviral.2020.104872. Epub 2020 Aug 5.
Antiviral Res. 2020.
PMID: 32768412
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Mcph1, mutated in primary microcephaly, is also crucial for erythropoiesis.
Vial Y, Nardelli J, Bonnard AA, Rousselot J, Souyri M, Gressens P, Cavé H, Drunat S.
Vial Y, et al.
EMBO Rep. 2024 Apr 11. doi: 10.1038/s44319-024-00123-8. Online ahead of print.
EMBO Rep. 2024.
PMID: 38605277
Free article.
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Down syndrome-like acute megakaryoblastic leukemia in a patient with Cornelia de Lange syndrome.
Vial Y, Lachenaud J, Verloes A, Besnard M, Fenneteau O, Lainey E, Marceau-Renaut A, Preudhomme C, Baruchel A, Cavé H, Drunat S.
Vial Y, et al.
Haematologica. 2018 Jun;103(6):e274-e276. doi: 10.3324/haematol.2017.178590. Epub 2017 Dec 7.
Haematologica. 2018.
PMID: 29217785
Free PMC article.
No abstract available.
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Detection of SARS-CoV-2 N-antigen in blood during acute COVID-19 provides a sensitive new marker and new testing alternatives.
Hingrat QL, Visseaux B, Laouenan C, Tubiana S, Bouadma L, Yazdanpanah Y, Duval X, Burdet C, Ichou H, Damond F, Bertine M, Benmalek N, Choquet C, Timsit JF, Ghosn J, Charpentier C, Descamps D, Houhou-Fidouh N; French COVID cohort management committee, CoV-CONTACT study group; members of the French-COVID cohort study group (by alphabetical order); member of the CoV-CONTACT study group. Principal investigator; Steering Committee; CoV-CONTACT Clinical Centers; Coordination and statistical analyses; Virological Lab; Biological Center; Partners; Sponsor; Genetic.
Hingrat QL, et al.
Clin Microbiol Infect. 2020 Dec 8;27(5):789.e1-5. doi: 10.1016/j.cmi.2020.11.025. Online ahead of print.
Clin Microbiol Infect. 2020.
PMID: 33307227
Free PMC article.
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Insertion of an extra copy of Xq22.2 into 1p36 results in functional duplication of the PLP1 gene in a girl with classical Pelizaeus-Merzbacher disease.
Masliah-Planchon J, Dupont C, Vartzelis G, Trimouille A, Eymard-Pierre E, Gay-Bellile M, Renaldo F, Dorboz I, Pagan C, Quentin S, Elmaleh M, Kotsogianni C, Konstantelou E, Drunat S, Tabet AC, Boespflug-Tanguy O.
Masliah-Planchon J, et al.
BMC Med Genet. 2015 Sep 2;16:77. doi: 10.1186/s12881-015-0226-6.
BMC Med Genet. 2015.
PMID: 26329556
Free PMC article.
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