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

Year Number of Results
1987 1
1988 3
1989 3
1990 2
1991 3
1992 3
1993 5
1994 1
1995 2
1996 1
1997 4
1998 4
1999 3
2000 2
2001 4
2002 3
2003 2
2004 3
2005 2
2006 3
2007 2
2008 2
2009 6
2010 4
2011 6
2012 9
2013 8
2014 8
2015 10
2016 4
2017 4
2018 5
2019 6
2020 7
2021 7
2022 5
2023 2
2024 0

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131 results

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Page 1
Inherited thrombocytopenias.
Balduini CL, Noris P. Balduini CL, et al. Among authors: noris p. Hematology. 2015 Jul;20(6):374-5. doi: 10.1179/1024533215Z.000000000374. Hematology. 2015. PMID: 26084367 No abstract available.
Platelet count and aging.
Balduini CL, Noris P. Balduini CL, et al. Among authors: noris p. Haematologica. 2014 Jun;99(6):953-5. doi: 10.3324/haematol.2014.106260. Haematologica. 2014. PMID: 24881040 Free PMC article. No abstract available.
Hereditary thrombocytopenias: a growing list of disorders.
Noris P, Pecci A. Noris P, et al. Hematology Am Soc Hematol Educ Program. 2017 Dec 8;2017(1):385-399. doi: 10.1182/asheducation-2017.1.385. Hematology Am Soc Hematol Educ Program. 2017. PMID: 29222283 Free PMC article. Review.
Inherited thrombocytopenias: the evolving spectrum.
Balduini CL, Pecci A, Noris P. Balduini CL, et al. Among authors: noris p. Hamostaseologie. 2012;32(4):259-70. doi: 10.5482/ha12050001. Epub 2012 Sep 13. Hamostaseologie. 2012. PMID: 22972471 Review.
Diagnosis and management of inherited thrombocytopenias.
Balduini CL, Pecci A, Noris P. Balduini CL, et al. Among authors: noris p. Semin Thromb Hemost. 2013 Mar;39(2):161-71. doi: 10.1055/s-0032-1333540. Epub 2013 Feb 8. Semin Thromb Hemost. 2013. PMID: 23397552 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. Among authors: noris p. Hum Mutat. 2014 Sep;35(9):1033-45. doi: 10.1002/humu.22607. Epub 2014 Jul 15. Hum Mutat. 2014. PMID: 24934643 Review.
Expert opinion on the use of platelet secretion assay for the diagnosis of inherited platelet function disorders: Communication from the ISTH SSC Subcommittee on Platelet Physiology.
Mezzano D, Harrison P, Frelinger AL 3rd, Mumford AD, Noris P, Lordkipanidzé M, Gresele P. Mezzano D, et al. Among authors: noris p. J Thromb Haemost. 2022 Sep;20(9):2127-2135. doi: 10.1111/jth.15781. Epub 2022 Jun 30. J Thromb Haemost. 2022. PMID: 35770723 Free article. Review.
Exome sequencing in 116 patients with inherited thrombocytopenia that remained of unknown origin after systematic phenotype-driven diagnostic workup.
Marconi C, Pecci A, Palombo F, Melazzini F, Bottega R, Nardi E, Bozzi V, Faleschini M, Barozzi S, Giangregorio T, Magini P, Balduini CL, Savoia A, Seri M, Noris P, Pippucci T. Marconi C, et al. Among authors: noris p. Haematologica. 2023 Jul 1;108(7):1909-1919. doi: 10.3324/haematol.2022.280993. Haematologica. 2023. PMID: 36519321 Free PMC article.
131 results