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

Year Number of Results
2007 3
2008 5
2009 2
2010 3
2011 2
2012 2
2013 3
2014 7
2015 9
2016 12
2017 7
2018 6
2019 10
2020 6
2021 9
2022 8
2023 7
2024 1

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85 results

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Page 1
Biallelic PRKAG2 Truncating Variants Are Associated with Severe Neonatal Cardiomyopathies.
Janin A, Gouy E, Putoux A, Perouse-de-Monclos T, Chevalier P, Faucherre A, Mancilla Abaroa J, Jopling C, Collardeau Frachon S, Radojevic J, El Chehadeh S, Millat G. Janin A, et al. Among authors: collardeau frachon s. Circ Genom Precis Med. 2023 Jun;16(3):277-279. doi: 10.1161/CIRCGEN.122.003881. Epub 2023 Apr 4. Circ Genom Precis Med. 2023. PMID: 37013823 Free article. No abstract available.
[Placental mesenchymal dysplasia].
Allias F, Lebreton F, Collardeau-Frachon S, Vasiljevic A, Rossignol S, Massardier J, Huissoud C, Devouassoux-Shisheboran M. Allias F, et al. Among authors: collardeau frachon s. Ann Pathol. 2008 Apr;28(2):85-94. doi: 10.1016/j.annpat.2008.03.005. Epub 2008 Jul 2. Ann Pathol. 2008. PMID: 18675158 French.
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: collardeau frachon s. 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.
A quest for Q fever.
Olivier-Gougenheim L, Freychet C, Collardeau-Frachon S, Roure-Sobas C, Di Filippo S, Riva R, Lega JC, Belot A. Olivier-Gougenheim L, et al. Among authors: collardeau frachon s. Lancet. 2019 Aug 3;394(10196):419. doi: 10.1016/S0140-6736(19)31675-7. Lancet. 2019. PMID: 31379332 No abstract available.
DCDC2 Mutations Cause Neonatal Sclerosing Cholangitis.
Girard M, Bizet AA, Lachaux A, Gonzales E, Filhol E, Collardeau-Frachon S, Jeanpierre C, Henry C, Fabre M, Viremouneix L, Galmiche L, Debray D, Bole-Feysot C, Nitschke P, Pariente D, Guettier C, Lyonnet S, Heidet L, Bertholet A, Jacquemin E, Henrion-Caude A, Saunier S. Girard M, et al. Among authors: collardeau frachon s. Hum Mutat. 2016 Oct;37(10):1025-9. doi: 10.1002/humu.23031. Epub 2016 Aug 24. Hum Mutat. 2016. PMID: 27319779
Radiographic features of the skeleton in disorders of post-squalene cholesterol biosynthesis.
Rossi M, Hall CM, Bouvier R, Collardeau-Frachon S, Le Breton F, Bucourt M, Cordier MP, Vianey-Saban C, Parenti G, Andria G, Le Merrer M, Edery P, Offiah AC. Rossi M, et al. Among authors: collardeau frachon s. Pediatr Radiol. 2015 Jul;45(7):965-76. doi: 10.1007/s00247-014-3257-9. Epub 2015 Feb 3. Pediatr Radiol. 2015. PMID: 25646736 Review.
Fetal phenotypes in otopalatodigital spectrum disorders.
Naudion S, Moutton S, Coupry I, Sole G, Deforges J, Guerineau E, Hubert C, Deves S, Pilliod J, Rooryck C, Abel C, Le Breton F, Collardeau-Frachon S, Cordier MP, Delezoide AL, Goldenberg A, Loget P, Melki J, Odent S, Patrier S, Verloes A, Viot G, Blesson S, Bessières B, Lacombe D, Arveiler B, Goizet C, Fergelot P. Naudion S, et al. Among authors: collardeau frachon s. Clin Genet. 2016 Mar;89(3):371-7. doi: 10.1111/cge.12679. Epub 2015 Oct 29. Clin Genet. 2016. PMID: 26404489
85 results