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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1965 1
1967 1
1968 1
1969 2
1978 1
1982 1
1996 1
2001 2
2005 1
2006 2
2007 1
2009 2
2013 1
2017 3
2018 3
2019 3
2021 1
2022 2
2023 1
2024 1
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29 results

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Page 1
L’administration des médicaments chez l’enfant.
Saint-Lorant G, Jéhan M, Chatelier N, Arion A. Saint-Lorant G, et al. Among authors: arion a. Rev Infirm. 2018 Oct;67(244):49-50. doi: 10.1016/j.revinf.2018.08.016. Rev Infirm. 2018. PMID: 30415693 French. No abstract available.
A severe pediatric life-threatening metabolic ketoacidosis.
Roulland C, Le Pallec C, Faucon C, Andre CO, Arion A, Goyer I, Brossier D. Roulland C, et al. Among authors: arion a. J Diabetes Metab Disord. 2024 Mar 25;23(1):1415-1418. doi: 10.1007/s40200-024-01410-w. eCollection 2024 Jun. J Diabetes Metab Disord. 2024. PMID: 38932849 Free PMC article.
Non-coding cis-regulatory variants in HK1 cause congenital hyperinsulinism with variable disease severity.
Bennett JJ, Saint-Martin C, Neumann B, Männistö JME, Houghton JAL, Empting S, Johnson MB, Laver TW, Locke JM, Spurrier B, Wakeling MN, Banerjee I, Dastamani A, Demirbilek H, Mitchell J, Stange M; International Congenital Hyperinsulinism Consortium; Mohnike K, Arnoux JB, Owens NDL, Zenker M, Bellanné-Chantelot C, Flanagan SE. Bennett JJ, et al. Genome Med. 2025 Mar 3;17(1):17. doi: 10.1186/s13073-025-01440-w. Genome Med. 2025. PMID: 40033430 Free PMC article.
Bronconeumopatías agudas del niño.
Brouard J, Vabret A, Nimal-Cuvillon D, Bach N, Bessière A, Arion A, Freymuth F. Brouard J, et al. Among authors: arion a. EMC Pediatr. 2009;44(1):1-16. doi: 10.1016/S1245-1789(09)70209-4. Epub 2011 Aug 10. EMC Pediatr. 2009. PMID: 32308523 Free PMC article. Spanish.
Association between acute complications in PMM2-CDG patients and haemostasis anomalies: Data from a multicentric study and suggestions for acute management.
Wicker C, Roux CJ, Goujon L, de Feraudy Y, Hully M, Brassier A, Bérat CM, Chemaly N, Wiedemann A, Damaj L, Abi-Warde MT, Dobbelaere D, Roubertie A, Cano A, Arion A, Kaminska A, Da Costa S, Bruneel A, Vuillaumier-Barrot S, Boddaert N, Pascreau T, Borgel D, Kossorotoff M, Harroche A, de Lonlay P. Wicker C, et al. Among authors: arion a. Mol Genet Metab. 2023 Nov;140(3):107674. doi: 10.1016/j.ymgme.2023.107674. Epub 2023 Jul 31. Mol Genet Metab. 2023. PMID: 37542768
Influence of early identification and therapy on long-term outcomes in early-onset MTHFR deficiency.
Yverneau M, Leroux S, Imbard A, Gleich F, Arion A, Moreau C, Nassogne MC, Szymanowski M, Tardieu M, Touati G, Bueno M, Chapman KA, Chien YH, Huemer M, Ješina P, Janssen MCH, Kölker S, Kožich V, Lavigne C, Lund AM, Mochel F, Morris A, Pons MR, Porras-Hurtado GL, Benoist JF, Damaj L, Schiff M; E-HOD Consortium. Yverneau M, et al. Among authors: arion a. J Inherit Metab Dis. 2022 Jul;45(4):848-861. doi: 10.1002/jimd.12504. Epub 2022 May 9. J Inherit Metab Dis. 2022. PMID: 35460084 Free article.
29 results