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Results by year

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

Year Number of Results
1851 1
1948 1
1965 1
1966 3
1968 1
1969 1
1971 2
1974 3
1975 5
1976 4
1977 2
1978 5
1979 1
1981 1
1986 2
1987 5
1990 1
1993 1
1994 1
1995 1
1996 1
1997 1
2000 5
2001 3
2002 2
2003 1
2004 4
2005 1
2006 4
2007 2
2008 6
2009 6
2010 6
2011 1
2012 2
2013 1
2014 2
2015 2
2016 4
2017 3
2018 5
2019 4
2020 5
2021 6
2022 4
2023 5
2024 2

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124 results

Results by year

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Page 1
Diagnosis and management of Silver-Russell syndrome: first international consensus statement.
Wakeling EL, Brioude F, Lokulo-Sodipe O, O'Connell SM, Salem J, Bliek J, Canton AP, Chrzanowska KH, Davies JH, Dias RP, Dubern B, Elbracht M, Giabicani E, Grimberg A, Grønskov K, Hokken-Koelega AC, Jorge AA, Kagami M, Linglart A, Maghnie M, Mohnike K, Monk D, Moore GE, Murray PG, Ogata T, Petit IO, Russo S, Said E, Toumba M, Tümer Z, Binder G, Eggermann T, Harbison MD, Temple IK, Mackay DJ, Netchine I. Wakeling EL, et al. Among authors: canton ap. Nat Rev Endocrinol. 2017 Feb;13(2):105-124. doi: 10.1038/nrendo.2016.138. Epub 2016 Sep 2. Nat Rev Endocrinol. 2017. PMID: 27585961
Pathogenic variants in TNRC6B cause a genetic disorder characterised by developmental delay/intellectual disability and a spectrum of neurobehavioural phenotypes including autism and ADHD.
Granadillo JL, P A Stegmann A, Guo H, Xia K, Angle B, Bontempo K, Ranells JD, Newkirk P, Costin C, Viront J, Stumpel CT, Sinnema M, Panis B, Pfundt R, Krapels IPC, Klaassens M, Nicolai J, Li J, Jiang Y, Marco E, Canton A, Latronico AC, Montenegro L, Leheup B, Bonnet C, M Amudhavalli S, Lawson CE, McWalter K, Telegrafi A, Pearson R, Kvarnung M, Wang X, Bi W, Rosenfeld JA, Shinawi M. Granadillo JL, et al. Among authors: canton a. J Med Genet. 2020 Oct;57(10):717-724. doi: 10.1136/jmedgenet-2019-106470. Epub 2020 Mar 9. J Med Genet. 2020. PMID: 32152250
Global Citizenship Education.
Cantón A, Garcia BI. Cantón A, et al. New Dir Stud Leadersh. 2018 Dec;2018(160):21-30. doi: 10.1002/yd.20307. New Dir Stud Leadersh. 2018. PMID: 30382628
On Teething.
Canton A. Canton A. Am J Dent Sci. 1851 Oct;2(1):131-138. Am J Dent Sci. 1851. PMID: 30751059 Free PMC article. No abstract available.
The EMILIN protein family.
Colombatti A, Doliana R, Bot S, Canton A, Mongiat M, Mungiguerra G, Paron-Cilli S, Spessotto P. Colombatti A, et al. Among authors: canton a. Matrix Biol. 2000 Aug;19(4):289-301. doi: 10.1016/s0945-053x(00)00074-3. Matrix Biol. 2000. PMID: 10963989 Review.
Tubular regeneration.
Mangione F, Mazzucco G, Canton AD. Mangione F, et al. Among authors: canton ad. NDT Plus. 2008 Feb;1(1):51-52. doi: 10.1093/ndtplus/sfm007. Epub 2007 Dec 19. NDT Plus. 2008. PMID: 30792786 Free PMC article. No abstract available.
Pioneering studies on monogenic central precocious puberty.
Canton APM, Seraphim CE, Brito VN, Latronico AC. Canton APM, et al. Arch Endocrinol Metab. 2019 Aug 22;63(4):438-444. doi: 10.20945/2359-3997000000164. Arch Endocrinol Metab. 2019. PMID: 31460623 Free PMC article. Review.
LipoDDx: a mobile application for identification of rare lipodystrophy syndromes.
Araújo-Vilar D, Fernández-Pombo A, Rodríguez-Carnero G, Martínez-Olmos MÁ, Cantón A, Villar-Taibo R, Hermida-Ameijeiras Á, Santamaría-Nieto A, Díaz-Ortega C, Martínez-Rey C, Antela A, Losada E, Muy-Pérez AE, González-Méndez B, Sánchez-Iglesias S. Araújo-Vilar D, et al. Among authors: canton a. Orphanet J Rare Dis. 2020 Apr 2;15(1):81. doi: 10.1186/s13023-020-01364-1. Orphanet J Rare Dis. 2020. PMID: 32241282 Free PMC article.
124 results