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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 8
2010 6
2011 1
2012 3
2013 3
2014 3
2015 2
2016 4
2017 3
2018 5
2019 4
2020 6
2021 7
2022 4
2023 5
2024 9
2025 5

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141 results

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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
Rare variants in the MECP2 gene in girls with central precocious puberty: a translational cohort study.
Canton APM, Tinano FR, Guasti L, Montenegro LR, Ryan F, Shears D, de Melo ME, Gomes LG, Piana MP, Brauner R, Espino-Aguilar R, Escribano-Muñoz A, Paganoni A, Read JE, Korbonits M, Seraphim CE, Costa SS, Krepischi AC, Jorge AAL, David A, Kaisinger LR, Ong KK, Perry JRB, Abreu AP, Kaiser UB, Argente J, Mendonca BB, Brito VN, Howard SR, Latronico AC. Canton APM, et al. Lancet Diabetes Endocrinol. 2023 Aug;11(8):545-554. doi: 10.1016/S2213-8587(23)00131-6. Epub 2023 Jun 26. Lancet Diabetes Endocrinol. 2023. PMID: 37385287 Free PMC article.
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
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.
DLK1 Is a Novel Link Between Reproduction and Metabolism.
Gomes LG, Cunha-Silva M, Crespo RP, Ramos CO, Montenegro LR, Canton A, Lees M, Spoudeas H, Dauber A, Macedo DB, Bessa DS, Maciel GA, Baracat EC, Jorge AAL, Mendonca BB, Brito VN, Latronico AC. Gomes LG, et al. Among authors: canton a. J Clin Endocrinol Metab. 2019 Jun 1;104(6):2112-2120. doi: 10.1210/jc.2018-02010. J Clin Endocrinol Metab. 2019. PMID: 30462238
Peripheral precocious puberty in girls with McCune-Albright syndrome: a case series.
Faria AG, Montenegro LR, Jorge AAL, Martin RM, Fragoso MCBV, Tinano FR, Seraphim CE, Canton APM, Gomes LG, Martos-Moreno GA, García IT, Carcavilla A, Tirado-Capistros M, Souza-Pinto NC, Argente J, Latronico AC, Mendonca BB, Brito VN. Faria AG, et al. Among authors: canton apm. Arch Endocrinol Metab. 2025 May 14;69(2):e240459. doi: 10.20945/2359-4292-2024-0459. Arch Endocrinol Metab. 2025. PMID: 40366083 Free PMC article.
141 results