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

Year Number of Results
1983 1
1989 1
1992 4
1993 2
1994 1
1997 1
2001 1
2003 1
2006 1
2008 2
2011 3
2012 2
2013 3
2014 4
2015 5
2016 7
2017 8
2018 5
2019 9
2020 8
2021 5
2022 10
2023 8
2024 7

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89 results

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Page 1
Vitamin D and calcium intakes in general pediatric populations: A French expert consensus paper.
Bacchetta J, Edouard T, Laverny G, Bernardor J, Bertholet-Thomas A, Castanet M, Garnier C, Gennero I, Harambat J, Lapillonne A, Molin A, Naud C, Salles JP, Laborie S, Tounian P, Linglart A. Bacchetta J, et al. Among authors: molin a. Arch Pediatr. 2022 May;29(4):312-325. doi: 10.1016/j.arcped.2022.02.008. Epub 2022 Mar 16. Arch Pediatr. 2022. PMID: 35305879 Free article.
Targeted next-generation sequencing in a large series of fetuses with severe renal diseases.
Jordan P, Dorval G, Arrondel C, Morinière V, Tournant C, Audrezet MP, Michel-Calemard L, Putoux A, Lesca G, Labalme A, Whalen S, Loeuillet L, Martinovic J, Attie-Bitach T, Bessières B, Schaefer E, Scheidecker S, Lambert L, Beneteau C, Patat O, Boute-Benejean O, Molin A, Guimiot F, Fontanarosa N, Nizon M, Lefebvre M, Jeanpierre C, Saunier S, Heidet L. Jordan P, et al. Among authors: molin a. Hum Mutat. 2022 Mar;43(3):347-361. doi: 10.1002/humu.24324. Epub 2022 Jan 10. Hum Mutat. 2022. PMID: 35005812
Consolidation of the clinical and genetic definition of a SOX4-related neurodevelopmental syndrome.
Angelozzi M, Karvande A, Molin AN, Ritter AL, Leonard JMM, Savatt JM, Douglass K, Myers SM, Grippa M, Tolchin D, Zackai E, Donoghue S, Hurst ACE, Descartes M, Smith K, Velasco D, Schmanski A, Crunk A, Tokita MJ, de Lange IM, van Gassen K, Robinson H, Guegan K, Suri M, Patel C, Bournez M, Faivre L, Tran-Mau-Them F, Baker J, Fabie N, Weaver K, Shillington A, Hopkin RJ, Barge-Schaapveld DQCM, Ruivenkamp CA, Bökenkamp R, Vergano S, Seco Moro MN, Díaz de Bustamante A, Misra VK, Kennelly K, Rogers C, Friedman J, Wigby KM, Lenberg J, Graziano C, Ahrens-Nicklas RC, Lefebvre V. Angelozzi M, et al. Among authors: molin an. J Med Genet. 2022 Nov;59(11):1058-1068. doi: 10.1136/jmedgenet-2021-108375. Epub 2022 Mar 1. J Med Genet. 2022. PMID: 35232796 Free PMC article.
One-Year Follow up of Noninvasive Respiratory Support in General Wards.
Moretto F, Fracazzini M, Verdina F, Ferrante D, Baino S, Grossi F, Castello L, Cammarota G, Balbo P, Sainaghi PP, Campanini M, Pirisi M, Patti G, Molin AD, Corte FD, Navalesi P, Vaschetto R. Moretto F, et al. Among authors: molin ad. Respir Care. 2022 Jul 19:respcare.09625. doi: 10.4187/respcare.09625. Online ahead of print. Respir Care. 2022. PMID: 35853702
A chromosome-anchored eggplant genome sequence reveals key events in Solanaceae evolution.
Barchi L, Pietrella M, Venturini L, Minio A, Toppino L, Acquadro A, Andolfo G, Aprea G, Avanzato C, Bassolino L, Comino C, Molin AD, Ferrarini A, Maor LC, Portis E, Reyes-Chin-Wo S, Rinaldi R, Sala T, Scaglione D, Sonawane P, Tononi P, Almekias-Siegl E, Zago E, Ercolano MR, Aharoni A, Delledonne M, Giuliano G, Lanteri S, Rotino GL. Barchi L, et al. Among authors: molin ad. Sci Rep. 2019 Aug 13;9(1):11769. doi: 10.1038/s41598-019-47985-w. Sci Rep. 2019. PMID: 31409808 Free PMC article.
Multiple molecular diagnoses in the field of intellectual disability and congenital anomalies: 3.5% of all positive cases.
Racine C, Denommé-Pichon AS, Engel C, Tran Mau-Them F, Bruel AL, Vitobello A, Safraou H, Sorlin A, Nambot S, Delanne J, Garde A, Colin E, Moutton S, Thevenon J, Jean-Marçais N, Willems M, Geneviève D, Pinson L, Perrin L, Laffargue F, Lespinasse J, Lacaze E, Molin A, Gerard M, Lambert L, Benigni C, Patat O; Orphanomix Physician's Group; Bourgeois V, Poe C, Chevarin M, Couturier V, Garret P, Philippe C, Duffourd Y, Faivre L, Thauvin-Robinet C. Racine C, et al. Among authors: molin a. J Med Genet. 2023 Dec 21;61(1):36-46. doi: 10.1136/jmg-2023-109170. J Med Genet. 2023. PMID: 37586840
89 results