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Characterization of RAGE and CK2 Expressions in Human Fetal Membranes.
Int J Mol Sci. 2023 Feb 17;24(4):4074. doi: 10.3390/ijms24044074.
Int J Mol Sci. 2023.
PMID: 36835482
Free PMC article.
Prenatal diagnosis of hemimegalencephaly revealing tuberous sclerosis complex.
Bruet S, Francannet C, Marguet F, Biard M, Sarret C, Laurichesse Delmas H.
Bruet S, et al.
Ultrasound Obstet Gynecol. 2020 May;55(5):688-689. doi: 10.1002/uog.21874.
Ultrasound Obstet Gynecol. 2020.
PMID: 31568608
Free article.
No abstract available.
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Systematic review of high-flow nasal cannula versus continuous positive airway pressure for primary support in preterm infants.
Bruet S, Butin M, Dutheil F.
Bruet S, et al.
Arch Dis Child Fetal Neonatal Ed. 2022 Jan;107(1):56-59. doi: 10.1136/archdischild-2020-321094. Epub 2021 May 20.
Arch Dis Child Fetal Neonatal Ed. 2022.
PMID: 34016651
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MYT1L mutations cause intellectual disability and variable obesity by dysregulating gene expression and development of the neuroendocrine hypothalamus.
Blanchet P, Bebin M, Bruet S, Cooper GM, Thompson ML, Duban-Bedu B, Gerard B, Piton A, Suckno S, Deshpande C, Clowes V, Vogt J, Turnpenny P, Williamson MP, Alembik Y; Clinical Sequencing Exploratory Research Study Consortium; Deciphering Developmental Disorders Consortium; Glasgow E, McNeill A.
Blanchet P, et al. Among authors: bruet s.
PLoS Genet. 2017 Aug 31;13(8):e1006957. doi: 10.1371/journal.pgen.1006957. eCollection 2017 Aug.
PLoS Genet. 2017.
PMID: 28859103
Free PMC article.
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