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

Year Number of Results
1999 1
2004 5
2005 4
2006 3
2008 2
2009 1
2011 4
2012 7
2013 5
2014 4
2015 8
2016 6
2017 5
2018 9
2019 8
2020 8
2021 6
2022 10
2023 6
2024 2

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88 results

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Page 1
Potential Role of Sphingolipidoses-Associated Lysosphingolipids in Cancer.
Dubot P, Astudillo L, Therville N, Carrié L, Pettazzoni M, Cheillan D, Stirnemann J, Levade T, Andrieu-Abadie N, Sabourdy F. Dubot P, et al. Among authors: cheillan d. Cancers (Basel). 2022 Oct 5;14(19):4858. doi: 10.3390/cancers14194858. Cancers (Basel). 2022. PMID: 36230781 Free PMC article. Review.
[Creatine deficiency syndromes].
Cheillan D, Cognat S, Vandenberghe N, Des Portes V, Vianey-Saban C. Cheillan D, et al. Rev Neurol (Paris). 2005 Mar;161(3):284-9. doi: 10.1016/s0035-3787(05)85034-9. Rev Neurol (Paris). 2005. PMID: 15800449 Review. French.
GM3 synthase deficiency in non-Amish patients.
Heide S, Jacquemont ML, Cheillan D, Renouil M, Tallot M, Schwartz CE, Miquel J, Bintner M, Rodriguez D, Darcel F, Buratti J, Haye D, Passemard S, Gras D, Perrin L, Capri Y, Gérard B, Piton A, Keren B, Thauvin-Robinet C, Duffourd Y, Faivre L, Poe C, Pervillé A, Héron D, Thévenon J, Arnaud L, LeGuern E, La Selva L, Vetro A, Guerrini R, Nava C, Mignot C. Heide S, et al. Among authors: cheillan d. Genet Med. 2022 Feb;24(2):492-498. doi: 10.1016/j.gim.2021.10.007. Epub 2021 Nov 30. Genet Med. 2022. PMID: 34906476 Free article.
Towards Achieving Equity and Innovation in Newborn Screening across Europe.
Sikonja J, Groselj U, Scarpa M, la Marca G, Cheillan D, Kölker S, Zetterström RH, Kožich V, Le Cam Y, Gumus G, Bottarelli V, van der Burg M, Dekkers E, Battelino T, Prevot J, Schielen PCJI, Bonham JR. Sikonja J, et al. Among authors: cheillan d. Int J Neonatal Screen. 2022 May 6;8(2):31. doi: 10.3390/ijns8020031. Int J Neonatal Screen. 2022. PMID: 35645285 Free PMC article. Review.
[Newborn screening in France: where are we going?].
Sarles J, Huet F, Cheillan D, Roussey M. Sarles J, et al. Among authors: cheillan d. Arch Pediatr. 2014 Aug;21(8):813-5. doi: 10.1016/j.arcped.2014.05.004. Epub 2014 Jun 27. Arch Pediatr. 2014. PMID: 24986067 French. No abstract available.
Creatine biosynthesis and transport in health and disease.
Joncquel-Chevalier Curt M, Voicu PM, Fontaine M, Dessein AF, Porchet N, Mention-Mulliez K, Dobbelaere D, Soto-Ares G, Cheillan D, Vamecq J. Joncquel-Chevalier Curt M, et al. Among authors: cheillan d. Biochimie. 2015 Dec;119:146-65. doi: 10.1016/j.biochi.2015.10.022. Epub 2015 Nov 2. Biochimie. 2015. PMID: 26542286 Review.
Neonatal screening for congenital hypothyroidism: Time to lower the TSH threshold in France.
Levaillant L, Huet F, Bretones P, Corne C, Dupuis C, Reynaud R, Somma C, Barat P, Corcuff JB, Bouhours-Nouet N, Gauthereau V, Polak M, Leger J, Cheillan D, Coutant R. Levaillant L, et al. Among authors: cheillan d. Arch Pediatr. 2022 May;29(4):253-257. doi: 10.1016/j.arcped.2022.02.001. Epub 2022 Mar 26. Arch Pediatr. 2022. PMID: 35351343 Review.
Antenatal manifestations of inborn errors of metabolism: biological diagnosis.
Vianey-Saban C, Acquaviva C, Cheillan D, Collardeau-Frachon S, Guibaud L, Pagan C, Pettazzoni M, Piraud M, Lamazière A, Froissart R. Vianey-Saban C, et al. Among authors: cheillan d. J Inherit Metab Dis. 2016 Sep;39(5):611-624. doi: 10.1007/s10545-016-9947-8. Epub 2016 Jul 8. J Inherit Metab Dis. 2016. PMID: 27393412 Review.
88 results