Similar articles for PMID: 19450438

Year	Number of Results
1923	1
1997	1
1998	1
2000	3
2001	4
2002	8
2003	13
2004	9
2005	12
2006	19
2007	25
2008	63
2009	82
2010	14
2011	10
2012	16
2013	16
2014	14
2015	7
2016	4
2017	6
2018	9
2019	8
2020	4
2021	5
2022	3
2023	2
2024	0

1

Identification of the first duplication in MYH9-related disease: a hot spot for unequal crossing-over within exon 24 of the MYH9 gene.

De Rocco D, Pujol-Moix N, Pecci A, Faletra F, Bozzi V, Balduini CL, Savoia A. De Rocco D, et al. Eur J Med Genet. 2009 Jul-Aug;52(4):191-4. doi: 10.1016/j.ejmg.2009.01.006. Epub 2009 Feb 9. Eur J Med Genet. 2009. PMID: 19450438

2

Identification of three in-frame deletion mutations in MYH9 disorders suggesting an important hot spot for small rearrangements in MYH9 exon 24.

Miyazaki K, Kunishima S, Fujii W, Higashihara M. Miyazaki K, et al. Eur J Haematol. 2009 Sep;83(3):230-4. doi: 10.1111/j.1600-0609.2009.01274.x. Epub 2009 May 4. Eur J Haematol. 2009. PMID: 19459928

3

Identification of the first in cis mutations in MYH9 disorder.

Miyajima Y, Kunishima S. Miyajima Y, et al. Eur J Haematol. 2009 Apr;82(4):288-91. doi: 10.1111/j.1600-0609.2008.01202.x. Epub 2008 Dec 19. Eur J Haematol. 2009. PMID: 19191864

4

[Autosomal dominant macrothrombocytopenia with leukocyte inclusion bodies and MYH9 disorders].

Kunishima S. Kunishima S. Rinsho Byori. 2009 Apr;57(4):365-70. Rinsho Byori. 2009. PMID: 19489439 Review. Japanese.

5

Analysis of clinical manifestations, mutant gene and encoded protein in two Chinese MYH9-related disease families.

Yi Y, Sen Zhang G, Xu M, San Ling Z, Ru Shao X, Zeng Li J, Ma J. Yi Y, et al. Clin Chim Acta. 2006 Nov;373(1-2):49-54. doi: 10.1016/j.cca.2006.04.027. Epub 2006 May 16. Clin Chim Acta. 2006. PMID: 16806139

6

Identification of six novel MYH9 mutations and genotype-phenotype relationships in autosomal dominant macrothrombocytopenia with leukocyte inclusions.

Kunishima S, Matsushita T, Kojima T, Amemiya N, Choi YM, Hosaka N, Inoue M, Jung Y, Mamiya S, Matsumoto K, Miyajima Y, Zhang G, Ruan C, Saito K, Song KS, Yoon HJ, Kamiya T, Saito H. Kunishima S, et al. J Hum Genet. 2001;46(12):722-9. doi: 10.1007/s100380170007. J Hum Genet. 2001. PMID: 11776386

7

Detection of unique neutrophil non-muscle myosin heavy chain-A localization by immunofluorescence analysis in MYH9 disorder presented with macrothrombocytopenia without leukocyte inclusions and deafness.

Kunishima S, Matsushita T, Shiratsuchi M, Ikuta T, Nishimura J, Hamaguchi M, Naoe T, Saito H. Kunishima S, et al. Eur J Haematol. 2005 Jan;74(1):1-5. doi: 10.1111/j.1600-0609.2004.00328.x. Eur J Haematol. 2005. PMID: 15613099

8

Clinical manifestation and molecular genetic characterization of MYH9 disorders.

Provaznikova D, Geierova V, Kumstyrova T, Kotlin R, Mikulenkova D, Zurkova K, Matoska V, Hrachovinova I, Rittich S. Provaznikova D, et al. Platelets. 2009 Aug;20(5):289-96. doi: 10.1080/09537100902993022. Platelets. 2009. PMID: 19557653

9

Alport syndrome. Molecular genetic aspects.

Hertz JM. Hertz JM. Dan Med Bull. 2009 Aug;56(3):105-52. Dan Med Bull. 2009. PMID: 19728970

10

MYH9-related platelet disorders.

Althaus K, Greinacher A. Althaus K, et al. Semin Thromb Hemost. 2009 Mar;35(2):189-203. doi: 10.1055/s-0029-1220327. Epub 2009 Apr 30. Semin Thromb Hemost. 2009. PMID: 19408192 Review.

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