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

Year Number of Results
2005 2
2006 1
2007 2
2008 1
2009 1
2010 1
2011 2
2012 1
2013 3
2014 3
2015 3
2016 1
2017 2
2018 2
2019 4
2020 5
2021 4
2022 2
2023 4
2024 1

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39 results

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Page 1
Unequal Impact of COL1A1 and COL1A2 Variants on Dentinogenesis Imperfecta.
Yamaguti PM, de La Dure-Molla M, Monnot S, Cardozo-Amaya YJ, Baujat G, Michot C, Fournier BPJ, Riou MC, Caldas Rosa ECC, Soares de Lima Y, Dos Santos PAC, Alcaraz G, Guerra ENS, Castro LC, de Oliveira SF, Pogue R, Berdal A, de Paula LM, Mazzeu JF, Cormier-Daire V, Acevedo AC. Yamaguti PM, et al. Among authors: monnot s. J Dent Res. 2023 Jun;102(6):616-625. doi: 10.1177/00220345231154569. Epub 2023 Mar 23. J Dent Res. 2023. PMID: 36951356
Assessing bleeding risk in 18 children with Osteogenesis imperfecta.
Léguillier T, Favier R, Harroche A, Lasne D, Bachelot-Loza C, Borgel D, Boussaroque A, Pascreau T, Lallemant-Dudek P, Gkalea V, Haguet MC, Cormier-Daire V, Beaudeux JL, Monnot S, Lapillonne H, Baujat G, Forin V, Nivet-Antoine V. Léguillier T, et al. Among authors: monnot s. Br J Haematol. 2021 Feb;192(4):785-788. doi: 10.1111/bjh.17303. Epub 2021 Jan 21. Br J Haematol. 2021. PMID: 33475155 No abstract available.
Innovative multi-modality imaging to assess paravalvular leak.
Isorni MA, Monnot S, Kloeckner M, Gerardin B, Hascoet S. Isorni MA, et al. Among authors: monnot s. Postepy Kardiol Interwencyjnej. 2019;15(1):120-122. doi: 10.5114/aic.2019.83778. Epub 2019 Apr 4. Postepy Kardiol Interwencyjnej. 2019. PMID: 31043995 Free PMC article. No abstract available.
FAM46A mutations are responsible for autosomal recessive osteogenesis imperfecta.
Doyard M, Bacrot S, Huber C, Di Rocco M, Goldenberg A, Aglan MS, Brunelle P, Temtamy S, Michot C, Otaify GA, Haudry C, Castanet M, Leroux J, Bonnefont JP, Munnich A, Baujat G, Lapunzina P, Monnot S, Ruiz-Perez VL, Cormier-Daire V. Doyard M, et al. Among authors: monnot s. J Med Genet. 2018 Apr;55(4):278-284. doi: 10.1136/jmedgenet-2017-104999. Epub 2018 Jan 22. J Med Genet. 2018. PMID: 29358272
39 results