Similar articles for PMID: 16098078

Year	Number of Results
1991	1
2000	3
2001	4
2002	6
2003	6
2004	4
2005	5
2006	7
2007	4
2008	7
2009	17
2010	8
2011	10
2012	11
2013	10
2014	7
2015	5
2016	8
2017	1
2018	5
2019	12
2020	11
2021	11
2022	4
2023	1
2024	1

1

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.

2

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.

3

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

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

Asp1424Asn MYH9 mutation results in an unstable protein responsible for the phenotypes in May-Hegglin anomaly/Fechtner syndrome.

Deutsch S, Rideau A, Bochaton-Piallat ML, Merla G, Geinoz A, Gabbiani G, Schwede T, Matthes T, Antonarakis SE, Beris P. Deutsch S, et al. Blood. 2003 Jul 15;102(2):529-34. doi: 10.1182/blood-2002-09-2783. Epub 2003 Mar 20. Blood. 2003. PMID: 12649151 Free article.

6

Mutation of MYH9, encoding non-muscle myosin heavy chain A, in May-Hegglin anomaly.

Kelley MJ, Jawien W, Ortel TL, Korczak JF. Kelley MJ, et al. Nat Genet. 2000 Sep;26(1):106-8. doi: 10.1038/79069. Nat Genet. 2000. PMID: 10973260

7

Nonmuscle Myosin Heavy Chain IIA Mutation Predicts Severity and Progression of Sensorineural Hearing Loss in Patients With MYH9-Related Disease.

Verver EJ, Topsakal V, Kunst HP, Huygen PL, Heller PG, Pujol-Moix N, Savoia A, Benazzo M, Fierro T, Grolman W, Gresele P, Pecci A. Verver EJ, et al. Ear Hear. 2016 Jan-Feb;37(1):112-20. doi: 10.1097/AUD.0000000000000198. Ear Hear. 2016. PMID: 26226608

8

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

9

[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.

10

High-resolution melting analysis for detection of MYH9 mutations.

Provaznikova D, Kumstyrova T, Kotlin R, Salaj P, Matoska V, Hrachovinova I, Rittich S. Provaznikova D, et al. Platelets. 2008 Sep;19(6):471-5. doi: 10.1080/09537100802140013. Platelets. 2008. PMID: 18925516

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