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Compared outcomes of very preterm infants born in 2000 and 2005.
Guerrot AM, Chadie A, Torre S, Rondeau S, Pinto Cardoso G, Abily-Donval L, Marret S; Perinatal Network of Haute-Normandie. Guerrot AM, et al. Among authors: rondeau s. Acta Paediatr. 2012 Jul;101(7):731-5. doi: 10.1111/j.1651-2227.2012.02678.x. Epub 2012 Apr 24. Acta Paediatr. 2012. PMID: 22452381
[Treatment of encephalopathy by hypothermia in the term newborn].
Marret S, Jadas V, Kieffer A, Chollat C, Rondeau S, Chadie A. Marret S, et al. Among authors: rondeau s. Arch Pediatr. 2014 Sep;21(9):1026-34. doi: 10.1016/j.arcped.2014.06.012. Epub 2014 Jul 28. Arch Pediatr. 2014. PMID: 25080834 Review. French.
[Interstitial pregnancy: experience at Rouen's hospital].
Douysset X, Verspyck E, Diguet A, Marpeau L, Chanavaz-Lacheray I, Rondeau S, Resch B, Sergent F. Douysset X, et al. Among authors: rondeau s. Gynecol Obstet Fertil. 2014 Apr;42(4):216-21. doi: 10.1016/j.gyobfe.2012.09.012. Epub 2013 Apr 18. Gynecol Obstet Fertil. 2014. PMID: 23602139 French.
Heterozygous UBR5 variants result in a neurodevelopmental syndrome with developmental delay, autism, and intellectual disability.
Sabeh P, Dumas SA, Maios C, Daghar H, Korzeniowski M, Rousseau J, Lines M, Guerin A, Millichap JJ, Landsverk M, Grebe T, Lindstrom K, Strober J, Ait Mouhoub T, Zweier C, Steinraths M, Hebebrand M, Callewaert B, Abou Jamra R, Kautza-Lucht M, Wegler M, Kruszka P, Kumps C, Banne E, Waberski MB, Dieux A, Raible S, Krantz I, Medne L, Pechter K, Villard L, Guerrini R, Bianchini C, Barba C, Mei D, Blanc X, Kallay C, Ranza E, Yang XR, O'Heir E, Donald KA, Murugasen S, Bruwer Z, Calikoglu M, Mathews JM, Lesieur-Sebellin M, Baujat G, Derive N, Pierson TM, Murrell JR, Shillington A, Ormieres C, Rondeau S, Reis A, Fernandez-Jaen A, Au PYB, Sweetser DA, Briere LC, Couque N, Perrin L, Schymick J, Gueguen P, Lefebvre M, Van Andel M, Juusola J, Antonarakis SE, Parker JA, Burnett BG, Campeau PM. Sabeh P, et al. Among authors: rondeau s. Am J Hum Genet. 2025 Jan 2;112(1):75-86. doi: 10.1016/j.ajhg.2024.11.009. Epub 2024 Dec 24. Am J Hum Genet. 2025. PMID: 39721588
Pathogenic SATB2 missense variants affecting p.Gly392 have variable functional implications and result in diverse clinical phenotypes.
den Hoed J, Hashimoto H, Khan M, Semmekrot F, Bosanko KA, Abe-Hatano C, Nakagawa E, Venselaar H, Quercia N, Chad L, Kurosaka H, Rondeau S, Fisher SE, Yamamoto S, Zarate YA. den Hoed J, et al. Among authors: rondeau s. J Med Genet. 2024 Oct 23;61(11):1062-1067. doi: 10.1136/jmg-2024-110015. J Med Genet. 2024. PMID: 39327041
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