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

Year Number of Results
1993 1
2001 1
2002 6
2003 4
2004 6
2005 2
2006 2
2007 3
2008 3
2009 6
2010 7
2011 5
2012 6
2013 6
2014 9
2015 5
2016 5
2017 5
2018 7
2019 3
2021 3
2022 6
2023 7
2024 1

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93 results

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Page 1
MYH9-Related Disease.
Savoia A, Pecci A. Savoia A, et al. 2008 Nov 20 [updated 2021 Feb 18]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2008 Nov 20 [updated 2021 Feb 18]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301740 Free Books & Documents. Review.
Identification of a robust DNA methylation signature for Fanconi anemia.
Pagliara D, Ciolfi A, Pedace L, Haghshenas S, Ferilli M, Levy MA, Miele E, Nardini C, Cappelletti C, Relator R, Pitisci A, De Vito R, Pizzi S, Kerkhof J, McConkey H, Nazio F, Kant SG, Di Donato M, Agolini E, Matraxia M, Pasini B, Pelle A, Galluccio T, Novelli A, Barakat TS, Andreani M, Rossi F, Mecucci C, Savoia A, Sadikovic B, Locatelli F, Tartaglia M. Pagliara D, et al. Among authors: savoia a. Am J Hum Genet. 2023 Nov 2;110(11):1938-1949. doi: 10.1016/j.ajhg.2023.09.014. Epub 2023 Oct 20. Am J Hum Genet. 2023. PMID: 37865086 Free PMC article.
Inherited thrombocytopenias: molecular mechanisms.
Balduini CL, Savoia A. Balduini CL, et al. Among authors: savoia a. Semin Thromb Hemost. 2004 Oct;30(5):513-23. doi: 10.1055/s-2004-835672. Semin Thromb Hemost. 2004. PMID: 15497094 Review.
Spectrum of the mutations in Bernard-Soulier syndrome.
Savoia A, Kunishima S, De Rocco D, Zieger B, Rand ML, Pujol-Moix N, Caliskan U, Tokgoz H, Pecci A, Noris P, Srivastava A, Ward C, Morel-Kopp MC, Alessi MC, Bellucci S, Beurrier P, de Maistre E, Favier R, Hézard N, Hurtaud-Roux MF, Latger-Cannard V, Lavenu-Bombled C, Proulle V, Meunier S, Négrier C, Nurden A, Randrianaivo H, Fabris F, Platokouki H, Rosenberg N, HadjKacem B, Heller PG, Karimi M, Balduini CL, Pastore A, Lanza F. Savoia A, et al. Hum Mutat. 2014 Sep;35(9):1033-45. doi: 10.1002/humu.22607. Epub 2014 Jul 15. Hum Mutat. 2014. PMID: 24934643 Review.
Genetics of familial forms of thrombocytopenia.
Balduini CL, Savoia A. Balduini CL, et al. Among authors: savoia a. Hum Genet. 2012 Dec;131(12):1821-32. doi: 10.1007/s00439-012-1215-x. Epub 2012 Aug 11. Hum Genet. 2012. PMID: 22886561 Review.
MYH9 gene mutations associated with bleeding.
Savoia A, De Rocco D, Pecci A. Savoia A, et al. Platelets. 2017 May;28(3):312-315. doi: 10.1080/09537104.2017.1294250. Epub 2017 Apr 3. Platelets. 2017. PMID: 28368695 No abstract available.
93 results