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Results: 1 to 20 of 115

1.

A Trp33Arg mutation at exon 1 of the MYH9 gene in a Korean patient with May-Hegglin anomaly.

Jang MJ, Park HJ, Chong SY, Huh JY, Kim IH, Jang JH, Kim HJ, Oh D.

Yonsei Med J. 2012 May;53(3):662-6. doi: 10.3349/ymj.2012.53.3.662.

PMID:
22477015
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

[Analysis of gene mutation in a family featuring autosomal dominant May-Hegglin anomaly].

Feng Y, Guo X, Li L, Li J, Liu Z, Zhu X, Liu Q.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013 Jun;30(3):305-8. doi: 10.3760/cma.j.issn.1003-9406.2013.03.012. Chinese.

PMID:
23744320
[PubMed - indexed for MEDLINE]
3.

R1933X mutation in the MYH9 gene in May-Hegglin anomaly mimicking idiopathic thrombocytopenic purpura.

Sung CC, Lin SH, Chao TK, Chen YC.

J Formos Med Assoc. 2014 Jan;113(1):56-9. doi: 10.1016/j.jfma.2012.07.024. Epub 2013 Jun 10.

PMID:
23759689
[PubMed - indexed for MEDLINE]
4.

[The MYH9 syndrome: report of a new case with a new mutation of the MYH9 gene].

Schleinitz N, Favier R, Mazodier K, Difeo A, Ebbo M, Veit V, Berda-Haddad Y, Bernit E, Heudier P, Kaplanski G, Camoin L, Bardet V, Harle JR.

Rev Med Interne. 2006 Oct;27(10):783-6. Epub 2006 Aug 15. French.

PMID:
16978745
[PubMed - indexed for MEDLINE]
5.

[Identification of nonmuscle mysin heavy chain 9 gene mutation in a May-Hegglin anomaly family].

Zhang G, Yi Y, Xu M, Ling Z.

Zhonghua Yi Xue Za Zhi. 2002 Jul;82(13):918-20. Chinese.

PMID:
12126520
[PubMed - indexed for MEDLINE]
6.

[Clinical and molecular-biological study of a May-Hegglin anomaly family].

Shao XR, Li JZ, Ma J, Zhan ZM, Liang H, She XN, Lu HL, Wang LC, Jia CM, Wu LJ, Jin MH, Chen LJ.

Zhonghua Xue Ye Xue Za Zhi. 2004 Sep;25(9):548-51. Chinese.

PMID:
15569536
[PubMed - indexed for MEDLINE]
7.

[A non-familial May-Hegglin anomaly accompanying with MYH9 gene R1933X mutation and I1626V polymorphism].

Li Y, Wang YW, Zhang GS, Fang MY.

Zhonghua Xue Ye Xue Za Zhi. 2009 Sep;30(9):577-81. Chinese.

PMID:
19954613
[PubMed - indexed for MEDLINE]
8.

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.

Clin Chim Acta. 2006 Nov;373(1-2):49-54. Epub 2006 May 16.

PMID:
16806139
[PubMed - indexed for MEDLINE]
9.

[Clinical manifestations and gene mutations of a Chinese family with MYH9-related syndrome].

Shi RM, Cao XQ, Luo SF, Fang XL, Wang RH, Liu ZG.

Zhongguo Dang Dai Er Ke Za Zhi. 2012 Sep;14(9):678-82. Chinese.

PMID:
22989438
[PubMed - indexed for MEDLINE]
Free Article
10.

[Usefulness of immunofluorescence analysis of neutrophil nonmuscle myosin heavy chain-A for diagnosing in two sisters with May-Hegglin anomaly].

Kimura N, Matsumoto M, Matsumoto K, Asai N, Kunishima S.

Rinsho Ketsueki. 2008 Dec;49(12):1614-8. Japanese.

PMID:
19110523
[PubMed - indexed for MEDLINE]
11.

First description of somatic mosaicism in MYH9 disorders.

Kunishima S, Matsushita T, Yoshihara T, Nakase Y, Yokoi K, Hamaguchi M, Saito H.

Br J Haematol. 2005 Feb;128(3):360-5.

PMID:
15667538
[PubMed - indexed for MEDLINE]
12.

[Identification of MYH9 gene mutation in a May-Hegglin anomaly family].

Gao F, Hao JH, Wang ZL.

Zhonghua Xue Ye Xue Za Zhi. 2012 Aug;33(8):660-2. Chinese. No abstract available.

PMID:
23134864
[PubMed - indexed for MEDLINE]
Free Article
13.

[Nonmuscle myosin heavy chain 9 gene mutations related disease: a family report].

Hua Y, Wang F, Zhao Wh, Lu Ww, Zhang Hw, Li Jg, Ding J, Lu Xt.

Beijing Da Xue Xue Bao. 2008 Apr;40(2):160-4. Chinese.

PMID:
18458691
[PubMed - indexed for MEDLINE]
Free Article
14.

Identification of a novel MYH9 mutation in a patient with May-Hegglin anomaly.

Otsubo K, Kanegane H, Nomura K, Ogawa J, Miyawaki T, Kunishima S.

Pediatr Blood Cancer. 2006 Dec;47(7):968-9. No abstract available.

PMID:
16642488
[PubMed - indexed for MEDLINE]
15.

[Clinical and molecular study on Fechtner syndrome--case report and literature review].

Yang HY, Wang ZY, Su YH, Cao LJ, Bai X, Ruan CG.

Zhonghua Xue Ye Xue Za Zhi. 2007 Mar;28(3):160-4. Review. Chinese.

PMID:
17649707
[PubMed - indexed for MEDLINE]
16.

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

Kelley MJ, Jawien W, Ortel TL, Korczak JF.

Nat Genet. 2000 Sep;26(1):106-8.

PMID:
10973260
[PubMed - indexed for MEDLINE]
17.

Recent advances in the understanding and management of MYH9-related inherited thrombocytopenias.

Balduini CL, Pecci A, Savoia A.

Br J Haematol. 2011 Jul;154(2):161-74. doi: 10.1111/j.1365-2141.2011.08716.x. Epub 2011 May 4. Review.

PMID:
21542825
[PubMed - indexed for MEDLINE]
18.

Report of a young girl with MYH9 mutation and review of the literature.

Landi D, Lockhart E, Miller SE, Datto M, Rehder C, Kanaly A, Thornburg CD.

J Pediatr Hematol Oncol. 2012 Oct;34(7):538-40. Review.

PMID:
23007341
[PubMed - indexed for MEDLINE]
19.

Macrothrombocytopenia and progressive deafness is due to a mutation in MYH9.

Mhatre AN, Kim Y, Brodie HA, Lalwani AK.

Otol Neurotol. 2003 Mar;24(2):205-9.

PMID:
12621333
[PubMed - indexed for MEDLINE]
20.

[Case of an hemodialysis patient with MYH9 disorders].

Ishida R, Kusaba T, Kirita Y, Matsuoka E, Nakayama M, Uchiyama H, Kajita Y.

Nihon Jinzo Gakkai Shi. 2011;53(2):195-9. Japanese.

PMID:
21516706
[PubMed - indexed for MEDLINE]

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