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

Year Number of Results
1989 1
1990 3
1991 3
1994 2
1996 2
1998 1
1999 3
2000 2
2001 3
2002 1
2003 2
2004 2
2005 2
2006 3
2007 2
2008 2
2009 1
2010 1
2011 1
2015 1
2017 1
2018 2
2020 1
2021 2
2022 1
2023 2
2024 2

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44 results

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Page 1
[Mucinous lobular carcinoma].
Ab Der Halden C, Taillandier A, Bonneau C, Delalande F, Trehorel L, Michenet P. Ab Der Halden C, et al. Among authors: taillandier a. Ann Pathol. 2023 Jan;43(1):57-59. doi: 10.1016/j.annpat.2022.09.003. Epub 2022 Oct 19. Ann Pathol. 2023. PMID: 36270907 French. No abstract available.
[Story of a generalized histiocytosis].
Taillandier A, Chantreau PL, David C, Kerdraon R, Richard S, Michenet P. Taillandier A, et al. Ann Pathol. 2023 Nov;43(6):507-510. doi: 10.1016/j.annpat.2023.04.006. Epub 2023 May 9. Ann Pathol. 2023. PMID: 37169641 French. No abstract available.
[An emerging lymphoproliferative disorder].
Fort N, Taillandier A, Binois R, Kerdraon R, Kervarrec T, Delalande F. Fort N, et al. Among authors: taillandier a. Ann Pathol. 2024 Mar 18:S0242-6498(24)00071-3. doi: 10.1016/j.annpat.2024.02.011. Online ahead of print. Ann Pathol. 2024. PMID: 38503612 French. No abstract available.
[Basal cell carcinoma with myoepithelial differentiation].
David C, Taillandier A, Chantreau PL, Kerdraon R, Delalande F, Michenet P. David C, et al. Among authors: taillandier a. Ann Pathol. 2024 Mar 5:S0242-6498(24)00045-2. doi: 10.1016/j.annpat.2024.02.004. Online ahead of print. Ann Pathol. 2024. PMID: 38448266 French. No abstract available.
Genetic analysis of adults heterozygous for ALPL mutations.
Taillandier A, Domingues C, Dufour A, Debiais F, Guggenbuhl P, Roux C, Cormier C, Cortet B, Porquet-Bordes V, Coury F, Geneviève D, Chiesa J, Colin T, Fletcher E, Guichet A, Javier RM, Laroche M, Laurent M, Lausch E, LeHeup B, Lukas C, Schwabe G, van der Burgt I, Muti C, Simon-Bouy B, Mornet E. Taillandier A, et al. J Bone Miner Metab. 2018 Nov;36(6):723-733. doi: 10.1007/s00774-017-0888-6. Epub 2017 Dec 13. J Bone Miner Metab. 2018. PMID: 29236161
Utility of genetic testing for prenatal presentations of hypophosphatasia.
Sperelakis-Beedham B, Taillandier A, Domingues C, Guberto M, Colin E, Porquet-Bordes V, Rothenbuhler A, Salles JP, Wenkert D, Zankl A, Muti C, Bacrot S, Simon-Bouy B, Mornet E. Sperelakis-Beedham B, et al. Among authors: taillandier a. Mol Genet Metab. 2021 Mar;132(3):198-203. doi: 10.1016/j.ymgme.2021.01.009. Epub 2021 Jan 27. Mol Genet Metab. 2021. PMID: 33549410
A molecular approach to dominance in hypophosphatasia.
Lia-Baldini AS, Muller F, Taillandier A, Gibrat JF, Mouchard M, Robin B, Simon-Bouy B, Serre JL, Aylsworth AS, Bieth E, Delanote S, Freisinger P, Hu JC, Krohn HP, Nunes ME, Mornet E. Lia-Baldini AS, et al. Among authors: taillandier a. Hum Genet. 2001 Jul;109(1):99-108. doi: 10.1007/s004390100546. Hum Genet. 2001. PMID: 11479741
44 results