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

Year Number of Results
1973 2
1976 1
1982 1
2005 1
2006 1
2007 2
2008 8
2009 3
2010 3
2011 3
2013 1
2014 3
2015 2
2016 3
2017 2
2018 3
2019 3
2020 2
2021 6
2022 4
2023 3
2024 1

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55 results

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Page 1
Prader-Willi syndrome: Hormone therapies.
Tauber M, Diene G. Tauber M, et al. Among authors: diene g. Handb Clin Neurol. 2021;181:351-367. doi: 10.1016/B978-0-12-820683-6.00026-9. Handb Clin Neurol. 2021. PMID: 34238470 Review.
[The Prader-Willi syndrome].
Diene G, Postel-Vinay A, Pinto G, Polak M, Tauber M. Diene G, et al. Ann Endocrinol (Paris). 2007 Jun;68(2-3):129-37. doi: 10.1016/j.ando.2007.03.002. Epub 2007 May 17. Ann Endocrinol (Paris). 2007. PMID: 17499572 Review. French.
A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing.
Denommé-Pichon AS, Matalonga L, de Boer E, Jackson A, Benetti E, Banka S, Bruel AL, Ciolfi A, Clayton-Smith J, Dallapiccola B, Duffourd Y, Ellwanger K, Fallerini C, Gilissen C, Graessner H, Haack TB, Havlovicova M, Hoischen A, Jean-Marçais N, Kleefstra T, López-Martín E, Macek M, Mencarelli MA, Moutton S, Pfundt R, Pizzi S, Posada M, Radio FC, Renieri A, Rooryck C, Ryba L, Safraou H, Schwarz M, Tartaglia M, Thauvin-Robinet C, Thevenon J, Tran Mau-Them F, Trimouille A, Votypka P, de Vries BBA, Willemsen MH, Zurek B, Verloes A, Philippe C; Solve-RD DITF-ITHACA; Solve-RD SNV-indel Working Group; Solve-RD Consortia; Orphanomix Group; Vitobello A, Vissers LELM, Faivre L. Denommé-Pichon AS, et al. Genet Med. 2023 Apr;25(4):100018. doi: 10.1016/j.gim.2023.100018. Epub 2023 Jan 20. Genet Med. 2023. PMID: 36681873 Free article.
First step towards a consensus strategy for multi-locus diagnostic testing of imprinting disorders.
Mackay D, Bliek J, Kagami M, Tenorio-Castano J, Pereda A, Brioude F, Netchine I, Papingi D, de Franco E, Lever M, Sillibourne J, Lombardi P, Gaston V, Tauber M, Diene G, Bieth E, Fernandez L, Nevado J, Tümer Z, Riccio A, Maher ER, Beygo J, Tannorella P, Russo S, de Nanclares GP, Temple IK, Ogata T, Lapunzina P, Eggermann T. Mackay D, et al. Among authors: diene g. Clin Epigenetics. 2022 Nov 7;14(1):143. doi: 10.1186/s13148-022-01358-9. Clin Epigenetics. 2022. PMID: 36345041 Free PMC article.
Sequelae of GH Treatment in Children with PWS.
Tauber M, Diene G, Molinas C. Tauber M, et al. Among authors: diene g. Pediatr Endocrinol Rev. 2016 Dec;14(2):138-146. doi: 10.17458/PER.2016.TDM.SequelaeofGH. Pediatr Endocrinol Rev. 2016. PMID: 28508607 Review.
Growth Hormone Treatment for Prader-Willi Syndrome.
Tauber M, Diene G, Molinas C. Tauber M, et al. Among authors: diene g. Pediatr Endocrinol Rev. 2018 Sep;16(Suppl 1):91-99. doi: 10.17458/per.vol16.2018.tdm.ghpraderwilli. Pediatr Endocrinol Rev. 2018. PMID: 30378786
Prader-Willi syndrome as a model of human hyperphagia.
Tauber M, Diene G, Mimoun E, Çabal-Berthoumieu S, Mantoulan C, Molinas C, Muscatelli F, Salles JP. Tauber M, et al. Among authors: diene g. Front Horm Res. 2014;42:93-106. doi: 10.1159/000358317. Epub 2014 Apr 7. Front Horm Res. 2014. PMID: 24732928 Review.
[Child obesity].
Tauber M, Jouret B, Diene G. Tauber M, et al. Among authors: diene g. Rev Prat. 2009 Sep 20;59(7):1005-12. Rev Prat. 2009. PMID: 19839478 French. No abstract available.
55 results