Similar articles for PMID: 11590545

Year	Number of Results
1985	1
1992	1
1993	1
1999	3
2000	5
2001	5
2002	8
2003	10
2004	5
2005	7
2006	8
2007	7
2008	14
2009	21
2010	13
2011	14
2012	14
2013	15
2014	14
2015	5
2016	7
2017	4
2018	12
2019	6
2020	14
2021	13
2022	11
2023	4
2024	1

1

Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly and Fechtner, Sebastian, Epstein, and Alport-like syndromes.

Heath KE, Campos-Barros A, Toren A, Rozenfeld-Granot G, Carlsson LE, Savige J, Denison JC, Gregory MC, White JG, Barker DF, Greinacher A, Epstein CJ, Glucksman MJ, Martignetti JA. Heath KE, et al. Am J Hum Genet. 2001 Nov;69(5):1033-45. doi: 10.1086/324267. Epub 2001 Oct 4. Am J Hum Genet. 2001. PMID: 11590545 Free PMC article.

2

Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium.

Seri M, Cusano R, Gangarossa S, Caridi G, Bordo D, Lo Nigro C, Ghiggeri GM, Ravazzolo R, Savino M, Del Vecchio M, d'Apolito M, Iolascon A, Zelante LL, Savoia A, Balduini CL, Noris P, Magrini U, Belletti S, Heath KE, Babcock M, Glucksman MJ, Aliprandis E, Bizzaro N, Desnick RJ, Martignetti JA. Seri M, et al. Nat Genet. 2000 Sep;26(1):103-5. doi: 10.1038/79063. Nat Genet. 2000. PMID: 10973259

3

Epstein syndrome: another renal disorder with mutations in the nonmuscle myosin heavy chain 9 gene.

Seri M, Savino M, Bordo D, Cusano R, Rocca B, Meloni I, Di Bari F, Koivisto PA, Bolognesi M, Ghiggeri GM, Landolfi R, Balduini CL, Zelante L, Ravazzolo R, Renieri A, Savoia A. Seri M, et al. Hum Genet. 2002 Feb;110(2):182-6. doi: 10.1007/s00439-001-0659-1. Epub 2001 Dec 14. Hum Genet. 2002. PMID: 11935325

4

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

5

[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.

6

Expression of the nonmuscle myosin heavy chain IIA in the human kidney and screening for MYH9 mutations in Epstein and Fechtner syndromes.

Arrondel C, Vodovar N, Knebelmann B, Grünfeld JP, Gubler MC, Antignac C, Heidet L. Arrondel C, et al. J Am Soc Nephrol. 2002 Jan;13(1):65-74. doi: 10.1681/ASN.V13165. J Am Soc Nephrol. 2002. PMID: 11752022

7

Cloning of the murine non-muscle myosin heavy chain IIA gene ortholog of human MYH9 responsible for May-Hegglin, Sebastian, Fechtner, and Epstein syndromes.

D'Apolito M, Guarnieri V, Boncristiano M, Zelante L, Savoia A. D'Apolito M, et al. Gene. 2002 Mar 20;286(2):215-22. doi: 10.1016/s0378-1119(02)00455-9. Gene. 2002. PMID: 11943476

8

[May-Hegglin anomaly--from genome research to clinical laboratory].

Kunishima S. Kunishima S. Rinsho Byori. 2003 Sep;51(9):898-904. Rinsho Byori. 2003. PMID: 14560660 Japanese.

9

Genotype-phenotype correlation in MYH9-related thrombocytopenia.

Dong F, Li S, Pujol-Moix N, Luban NL, Shin SW, Seo JH, Ruiz-Saez A, Demeter J, Langdon S, Kelley MJ. Dong F, et al. Br J Haematol. 2005 Aug;130(4):620-7. doi: 10.1111/j.1365-2141.2005.05658.x. Br J Haematol. 2005. PMID: 16098078 Free article.

10

Genetics, clinical and pathological features of glomerulonephritis associated with mutations of nonmuscle myosin IIA (Fechtner syndrome).

Ghiggeri GM, Caridi G, Magrini U, Sessa A, Savoia A, Seri M, Pecci A, Romagnoli R, Gangarossa S, Noris P, Sartore S, Necchi V, Ravazzolo R, Balduini CL. Ghiggeri GM, et al. Am J Kidney Dis. 2003 Jan;41(1):95-104. doi: 10.1053/ajkd.2003.50028. Am J Kidney Dis. 2003. PMID: 12500226

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