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

Year Number of Results
1992 1
1993 1
2004 1
2005 1
2006 2
2008 3
2009 1
2013 2
2015 1
2016 1
2017 1
2018 3
2019 1
2020 2
2023 0
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19 results
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Page 1
Clinical heterogeneity and phenotype/genotype findings in 5 families with GYG1 deficiency.
Ben Yaou R, Hubert A, Nelson I, Dahlqvist JR, Gaist D, Streichenberger N, Beuvin M, Krahn M, Petiot P, Parisot F, Michel F, Malfatti E, Romero N, Carlier RY, Eymard B, Labrune P, Duno M, Krag T, Cerino M, Bartoli M, Bonne G, Vissing J, Laforet P, Petit FM. Ben Yaou R, et al. Among authors: parisot f. Neurol Genet. 2017 Dec 18;3(6):e208. doi: 10.1212/NXG.0000000000000208. eCollection 2017 Dec. Neurol Genet. 2017. PMID: 29264399 Free PMC article.
The Tunisian population history through the Crigler-Najjar type I syndrome.
Petit FM, Bézieau S, Gajdos V, Parisot F, Scoul C, Capel L, Stozinic V, Khrouf N, M'Rad R, Koshy A, Mollet-Boudjemline A, Francoual J, Labrune P. Petit FM, et al. Among authors: parisot f. Eur J Hum Genet. 2008 Jul;16(7):848-53. doi: 10.1038/sj.ejhg.5201989. Epub 2008 Jan 16. Eur J Hum Genet. 2008. PMID: 18197191
Major discrepancy between factual antibiotic resistance and consumption in South of France: analysis of 539,037 bacterial strains.
Diallo OO, Baron SA, Dubourg G, Chaudet H, Halfon P, Camiade S, Comte B, Joubert S, François A, Seyral P, Parisot F, Casalta JP, Ruimy R, Maruejouls C, Achiardy JC, Burignat S, Carvajal J, Delaunay E, Meyer S, Levy PY, Roussellier P, Brunet P, Bosi C, Stolidi P, Arzouni JP, Gay G, Hance P, Colson P, Raoult D, Rolain JM. Diallo OO, et al. Among authors: parisot f. Sci Rep. 2020 Oct 26;10(1):18262. doi: 10.1038/s41598-020-75158-7. Sci Rep. 2020. PMID: 33106494 Free PMC article.
19 results