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Year Number of Results
1984 2
1986 1
1996 1
2002 1
2004 1
2007 1
2008 3
2009 2
2010 3
2011 2
2013 3
2014 2
2015 3
2016 3
2017 2
2018 1
2019 5
2020 2
2021 1
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38 results
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Page 1
Elements of morphology: Standard terminology for the teeth and classifying genetic dental disorders.
de La Dure-Molla M, Fournier BP, Manzanares MC, Acevedo AC, Hennekam RC, Friedlander L, Boy-Lefèvre ML, Kerner S, Toupenay S, Garrec P, Vi-Fane B, Felizardo R, Berteretche MV, Jordan L, Ferré F, Clauss F, Jung S, de Chalendar M, Troester S, Kawczynski M, Chaloyard J; International Group of Dental Nomenclature, Manière MC, Berdal A, Bloch-Zupan A. de La Dure-Molla M, et al. Among authors: maniere mc. Am J Med Genet A. 2019 Oct;179(10):1913-1981. doi: 10.1002/ajmg.a.61316. Epub 2019 Aug 29. Am J Med Genet A. 2019. PMID: 31468724
Only four genes (EDA1, EDAR, EDARADD, and WNT10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia cases.
Cluzeau C, Hadj-Rabia S, Jambou M, Mansour S, Guigue P, Masmoudi S, Bal E, Chassaing N, Vincent MC, Viot G, Clauss F, Manière MC, Toupenay S, Le Merrer M, Lyonnet S, Cormier-Daire V, Amiel J, Faivre L, de Prost Y, Munnich A, Bonnefont JP, Bodemer C, Smahi A. Cluzeau C, et al. Among authors: maniere mc. Hum Mutat. 2011 Jan;32(1):70-2. doi: 10.1002/humu.21384. Hum Mutat. 2011. PMID: 20979233
Multidisciplinary consensus recommendations from a European network for the diagnosis and practical management of patients with incontinentia pigmenti.
Bodemer C, Diociaiuti A, Hadj-Rabia S, Robert MP, Desguerre I, Manière MC, de la Dure-Molla M, De Liso P, Federici M, Galeotti A, Fusco F, Fraitag S, Demily C, Taieb C, Valeria Ursini M, El Hachem M, Steffann J. Bodemer C, et al. Among authors: maniere mc. J Eur Acad Dermatol Venereol. 2020 Jul;34(7):1415-1424. doi: 10.1111/jdv.16403. J Eur Acad Dermatol Venereol. 2020. PMID: 32678511
Efficacy, tolerability, and safety of an innovative medical device for improving oral accessibility during oral examination in special-needs patients: A multicentric clinical trial.
Mogenot M, Hein-Halbgewachs L, Goetz C, Ouamara N, Droz-Desprez D, Strazielle C, Albecker S, Mengus B, Strub M, Manière MC, Richardin P, Wang S, Piga G, Dalstein A, Anastasio D. Mogenot M, et al. Among authors: maniere mc. PLoS One. 2020 Sep 28;15(9):e0239898. doi: 10.1371/journal.pone.0239898. eCollection 2020. PLoS One. 2020. PMID: 32986784 Free PMC article. Clinical Trial.
A New SLC10A7 Homozygous Missense Mutation Responsible for a Milder Phenotype of Skeletal Dysplasia With Amelogenesis Imperfecta.
Laugel-Haushalter V, Bär S, Schaefer E, Stoetzel C, Geoffroy V, Alembik Y, Kharouf N, Huckert M, Hamm P, Hemmerlé J, Manière MC, Friant S, Dollfus H, Bloch-Zupan A. Laugel-Haushalter V, et al. Among authors: maniere mc. Front Genet. 2019 May 28;10:504. doi: 10.3389/fgene.2019.00504. eCollection 2019. Front Genet. 2019. PMID: 31191616 Free PMC article.
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