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Author Correction: Oesophageal atresia.
van Lennep M, Singendonk MMJ, Dall'Oglio L, Gottrand F, Krishnan U, Terheggen-Lagro SWJ, Omari TI, Benninga MA, van Wijk MP. van Lennep M, et al. Among authors: gottrand f. Nat Rev Dis Primers. 2024 Mar 22;10(1):24. doi: 10.1038/s41572-024-00513-1. Nat Rev Dis Primers. 2024. PMID: 38519551 No abstract available.
Refeeding Syndrome in Pediatric Age, An Unknown Disease: A Narrative Review.
Corsello A, Trovato CM, Dipasquale V, Bolasco G, Labriola F, Gottrand F, Verduci E, Diamanti A, Romano C. Corsello A, et al. Among authors: gottrand f. J Pediatr Gastroenterol Nutr. 2023 Dec 1;77(6):e75-e83. doi: 10.1097/MPG.0000000000003945. Epub 2023 Sep 14. J Pediatr Gastroenterol Nutr. 2023. PMID: 37705405 Free PMC article. Review.
[Idiopathic pulmonary fibrosis: Desperately seeking a model].
Hennion N, Chenivesse C, Humez S, Gottrand F, Desseyn JL, Gouyer V. Hennion N, et al. Among authors: gottrand f. Rev Mal Respir. 2024 Apr;41(4):274-278. doi: 10.1016/j.rmr.2024.02.009. Epub 2024 Mar 12. Rev Mal Respir. 2024. PMID: 38480096 Review. French.
Time to consider oesophageal atresia as a life-long disease.
Leroy M, Aumar M, Seguy D, Vandamme F, Widenmann A, Sfeir R, Gottrand F. Leroy M, et al. Among authors: gottrand f. Int J Surg. 2024 May 1;110(5):2506-2507. doi: 10.1097/JS9.0000000000001167. Int J Surg. 2024. PMID: 38376869 Free PMC article. No abstract available.
Interplay of the Mediterranean diet and genetic hypertension risk on blood pressure in European adolescents: Findings from the HELENA study.
Pérez-Gimeno G, Seral-Cortes M, Sabroso-Lasa S, Esteban LM, Widhalm K, Gottrand F, Stehle P, Meirhaeghe A, Muntaner M, Kafatos A, Gutierrez A, Manios Y, Anastasiou CA, Gonzalez-Gross M, Breidenassel C, Censi L, de Henauw S, Labayen I, Bueno-Lozano G, Rupérez AI, Moreno LA. Pérez-Gimeno G, et al. Among authors: gottrand f. Eur J Pediatr. 2024 May;183(5):2101-2110. doi: 10.1007/s00431-024-05435-4. Epub 2024 Feb 13. Eur J Pediatr. 2024. PMID: 38349423 Free PMC article.
Recurrent "outsider" intronic variation in the SLC5A6 gene causes severe mixed axonal and demyelinating neuropathy, cyclic vomiting and optic atrophy in 3 families from Maghreb.
Mansour-Hendili L, Gitiaux C, Harion M, Latouche C, Heron B, Stojkovic T, Rama M, Smol T, Sophie Jourdain A, Mention K, Nadjar Y, Schiff M, Lemale J, Ghoumid J, Gottrand F, Talbotec C, Rötig A, Funalot B, Desguerre I. Mansour-Hendili L, et al. Among authors: gottrand f. Front Genet. 2024 Jan 29;15:1352006. doi: 10.3389/fgene.2024.1352006. eCollection 2024. Front Genet. 2024. PMID: 38348452 Free PMC article.
680 results