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

Year Number of Results
1989 1
1990 1
1991 1
1993 1
1994 2
1995 1
1996 2
1997 3
1998 4
1999 9
2000 9
2001 9
2002 4
2003 7
2004 4
2005 4
2006 8
2007 2
2008 9
2009 12
2010 6
2011 5
2012 9
2013 15
2014 12
2015 14
2016 11
2017 10
2018 12
2019 7
2020 3
2021 7
2022 2
2023 7
2024 4

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193 results

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Page 1
[Congenital thrombocytopenia].
Kunishima S. Kunishima S. Rinsho Ketsueki. 2018;59(6):764-773. doi: 10.11406/rinketsu.59.764. Rinsho Ketsueki. 2018. PMID: 29973458 Review. Japanese.
Congenital macrothrombocytopenias.
Kunishima S, Saito H. Kunishima S, et al. Blood Rev. 2006 Mar;20(2):111-21. doi: 10.1016/j.blre.2005.08.001. Epub 2005 Sep 19. Blood Rev. 2006. PMID: 16169642 Review.
Giant platelet syndrome.
Saito H, Matsushita T, Yamamoto K, Kojima T, Kunishima S. Saito H, et al. Among authors: kunishima s. Hematology. 2005;10 Suppl 1:41-6. doi: 10.1080/10245330512331389881. Hematology. 2005. PMID: 16188632 Review. No abstract available.
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: kunishima s. Hum Mutat. 2014 Sep;35(9):1033-45. doi: 10.1002/humu.22607. Epub 2014 Jul 15. Hum Mutat. 2014. PMID: 24934643 Review.
Regulation of lipid synthesis in myelin modulates neural activity and is required for motor learning.
Kato D, Aoyama Y, Nishida K, Takahashi Y, Sakamoto T, Takeda I, Tatematsu T, Go S, Saito Y, Kunishima S, Cheng J, Hou L, Tachibana Y, Sugio S, Kondo R, Eto F, Sato S, Moorhouse AJ, Yao I, Kadomatsu K, Setou M, Wake H. Kato D, et al. Among authors: kunishima s. Glia. 2023 Nov;71(11):2591-2608. doi: 10.1002/glia.24441. Epub 2023 Jul 20. Glia. 2023. PMID: 37475643
Advances in the understanding of MYH9 disorders.
Kunishima S, Saito H. Kunishima S, et al. Curr Opin Hematol. 2010 Sep;17(5):405-10. doi: 10.1097/MOH.0b013e32833c069c. Curr Opin Hematol. 2010. PMID: 20601875 Review.
Expanding the genetic spectrum of TUBB1-related thrombocytopenia.
Palma-Barqueros V, Bury L, Kunishima S, Lozano ML, Rodríguez-Alen A, Revilla N, Bohdan N, Padilla J, Fernández-Pérez MP, de la Morena-Barrio ME, Marín-Quilez A, Benito R, López-Fernández MF, Marcellini S, Zamora-Cánovas A, Vicente V, Martínez C, Gresele P, Bastida JM, Rivera J. Palma-Barqueros V, et al. Among authors: kunishima s. Blood Adv. 2021 Dec 28;5(24):5453-5467. doi: 10.1182/bloodadvances.2020004057. Blood Adv. 2021. PMID: 34516618 Free PMC article.
Diagnostic delay of MYH9-related disorder in Japan.
Sakamoto A, Uchiyama T, Kaname T, Iguchi A, Ohara O, Ishimura M, Onum M, Kunishima S, Ishiguro A. Sakamoto A, et al. Among authors: kunishima s. Br J Haematol. 2024 Apr 22. doi: 10.1111/bjh.19484. Online ahead of print. Br J Haematol. 2024. PMID: 38650331
193 results