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

Year Number of Results
2002 4
2003 1
2004 4
2005 3
2006 7
2007 1
2008 5
2009 4
2010 11
2011 10
2012 10
2013 10
2014 11
2015 10
2016 13
2017 12
2018 10
2019 13
2020 12
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Search Results

132 results
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Page 1
Pathophysiology of cerebral palsy.
Marret S, Vanhulle C, Laquerriere A. Marret S, et al. Among authors: laquerriere a. Handb Clin Neurol. 2013;111:169-76. doi: 10.1016/B978-0-444-52891-9.00016-6. Handb Clin Neurol. 2013. PMID: 23622161 Review.
Pineoblastoma segregates into molecular sub-groups with distinct clinico-pathologic features: a Rare Brain Tumor Consortium registry study.
Li BK, Vasiljevic A, Dufour C, Yao F, Ho BLB, Lu M, Hwang EI, Gururangan S, Hansford JR, Fouladi M, Nobusawa S, Laquerriere A, Delisle MB, Fangusaro J, Forest F, Toledano H, Solano-Paez P, Leary S, Birks D, Hoffman LM, Szathmari A, Faure-Conter C, Fan X, Catchpoole D, Zhou L, Schultz KAP, Ichimura K, Gauchotte G, Jabado N, Jones C, Loussouarn D, Mokhtari K, Rousseau A, Ziegler DS, Tanaka S, Pomeroy SL, Gajjar A, Ramaswamy V, Hawkins C, Grundy RG, Hill DA, Bouffet E, Huang A, Jouvet A. Li BK, et al. Among authors: laquerriere a. Acta Neuropathol. 2020 Feb;139(2):223-241. doi: 10.1007/s00401-019-02111-y. Epub 2019 Dec 9. Acta Neuropathol. 2020. PMID: 31820118
Early fetal presentation of Koolen-de Vries: Case report with literature review.
Sauvestre F, Marguet F, Rooryck C, Vuillaume ML, Cardinaud F, Laquerrière A, André G, Pelluard F. Sauvestre F, et al. Among authors: laquerriere a. Eur J Med Genet. 2017 Nov;60(11):605-609. doi: 10.1016/j.ejmg.2017.08.012. Epub 2017 Aug 12. Eur J Med Genet. 2017. PMID: 28811189 Review.
Pontocerebellar hypoplasia with rhombencephalosynapsis and microlissencephaly expands the spectrum of PCH type 1B.
Saugier-Veber P, Marguet F, Vezain M, Bucourt M, Letard P, Delahaye A, Pipiras E, Frébourg T, Gonzalez B, Laquerrière A. Saugier-Veber P, et al. Among authors: laquerriere a. Eur J Med Genet. 2020 Apr;63(4):103814. doi: 10.1016/j.ejmg.2019.103814. Epub 2019 Nov 23. Eur J Med Genet. 2020. PMID: 31770597
[Fetal alcohol exposure: when placenta would help to the early diagnosis of child brain impairments].
Sautreuil C, Laquerrière A, Lecuyer M, Brasse-Lagnel C, Jégou S, Bekri S, Marcorelles P, Gil S, Marret S, Gonzalez BJ. Sautreuil C, et al. Among authors: laquerriere a. Med Sci (Paris). 2019 Nov;35(11):859-865. doi: 10.1051/medsci/2019167. Epub 2019 Dec 17. Med Sci (Paris). 2019. PMID: 31845877 Free article. Review. French.
Metabolic causes of nonimmune hydrops fetalis: A next-generation sequencing panel as a first-line investigation.
Sudrié-Arnaud B, Marguet F, Patrier S, Martinovic J, Louillet F, Broux F, Charbonnier F, Dranguet H, Coutant S, Vezain M, Lanos R, Tebani A, Fuller M, Lamari F, Chambon P, Brehin AC, Trestard L, Tournier I, Marret S, Verspyck E, Laquerrière A, Bekri S. Sudrié-Arnaud B, et al. Among authors: laquerriere a. Clin Chim Acta. 2018 Jun;481:1-8. doi: 10.1016/j.cca.2018.02.023. Epub 2018 Feb 22. Clin Chim Acta. 2018. PMID: 29476731
Fraser syndrome: features suggestive of prenatal diagnosis in a review of 38 cases.
Tessier A, Sarreau M, Pelluard F, André G, Blesson S, Bucourt M, Dechelotte P, Faivre L, Frébourg T, Goldenberg A, Goua V, Jeanne-Pasquier C, Guimiot F, Laquerriere A, Laurent N, Lefebvre M, Loget P, Maréchaud M, Mechler C, Perez MJ, Sabourin JC, Verloes A, Patrier S, Guerrot AM. Tessier A, et al. Among authors: laquerriere a. Prenat Diagn. 2016 Dec;36(13):1270-1275. doi: 10.1002/pd.4971. Epub 2016 Dec 9. Prenat Diagn. 2016. PMID: 27859469 Review.
Basal ganglia involvement in ARX patients: The reason for ARX patients very specific grasping?
Curie A, Friocourt G, des Portes V, Roy A, Nazir T, Brun A, Cheylus A, Marcorelles P, Retzepi K, Maleki N, Bussy G, Paulignan Y, Reboul A, Ibarrola D, Kong J, Hadjikhani N, Laquerrière A, Gollub RL. Curie A, et al. Among authors: laquerriere a. Neuroimage Clin. 2018 Apr 5;19:454-465. doi: 10.1016/j.nicl.2018.04.001. eCollection 2018. Neuroimage Clin. 2018. PMID: 29984154 Free PMC article.
Phenotypic and Neuropathological Characterization of Fetal Pyruvate Dehydrogenase Deficiency.
Pirot N, Crahes M, Adle-Biassette H, Soares A, Bucourt M, Boutron A, Carbillon L, Mignot C, Trestard L, Bekri S, Laquerrière A. Pirot N, et al. Among authors: laquerriere a. J Neuropathol Exp Neurol. 2016 Mar;75(3):227-38. doi: 10.1093/jnen/nlv022. Epub 2016 Feb 9. J Neuropathol Exp Neurol. 2016. PMID: 26865159
Giant epidermoid cyst of the occipital area with bone invasion: A case report.
Alorini M, Vianney G, Florent M, Olivier L, Annie L. Alorini M, et al. Among authors: annie l. Int J Health Sci (Qassim). 2018 Jul-Aug;12(4):92-93. Int J Health Sci (Qassim). 2018. PMID: 30022910 Free PMC article.
132 results
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