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Items: 1 to 20 of 108

1.

[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
2.

[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
3.

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
4.

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.

5.

Advances in the understanding of MYH9 disorders.

Kunishima S, Saito H.

Curr Opin Hematol. 2010 Sep;17(5):405-10. doi: 10.1097/MOH.0b013e32833c069c. Review.

PMID:
20601875
6.

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
7.

[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
8.

Germinal mosaicism in MYH9 disorders: a family with two affected siblings of normal parents.

Kunishima S, Takaki K, Ito Y, Saito H.

Br J Haematol. 2009 Apr;145(2):260-2. doi: 10.1111/j.1365-2141.2009.07584.x. Epub 2009 Feb 4. No abstract available.

PMID:
19208103
9.

May-Hegglin anomaly: morphologic and clinical manifestations.

Saito H, Kunishima S.

Clin Adv Hematol Oncol. 2009 Feb;7(2):111-3. No abstract available.

PMID:
19367252
10.

Hematologic and genetic characterization of an MYH9-related disorder in a Chinese family.

Ma ES, Wong CL, Shek TW, Hui SP.

Haematologica. 2006 Jul;91(7):1002-3.

11.

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

Kunishima S.

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

PMID:
19489439
12.

[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
13.

A case of MYH9 disorders caused by a novel mutation (p.K74E).

Kanematsu T, Suzuki N, Yoshida T, Kishimoto M, Aoki T, Ogawa M, Kagami Y, Kiyoi H, Matsushita T, Kunishima S.

Ann Hematol. 2016 Jan;95(1):161-3. doi: 10.1007/s00277-015-2506-9. Epub 2015 Sep 17. No abstract available.

PMID:
26382273
14.

MYH9 related platelet disorders - often unknown and misdiagnosed.

Althaus K, Najm J, Greinacher A.

Klin Padiatr. 2011 May;223(3):120-5. doi: 10.1055/s-0031-1275664. Epub 2011 May 12. Review.

PMID:
21567368
15.

Description of a novel mutation leading to MYH9-related disease.

Burt RA, Joseph JE, Milliken S, Collinge JE, Kile BT.

Thromb Res. 2008;122(6):861-3. doi: 10.1016/j.thromres.2008.06.011. Epub 2008 Aug 3. No abstract available.

PMID:
18676005
16.

The first report of homozygous May-Hegglin anomaly E1841K mutation.

Poopak B, Rezvani H, Difeo A, Martignetti JA, Khosravipour G, Yousefian A, Farahani K, Haghnejad Doshanlo F, Saki N.

Eur J Haematol. 2011 Apr;86(4):357. doi: 10.1111/j.1600-0609.2010.01553.x. Epub 2011 Jan 11. No abstract available.

PMID:
21083612
17.

A rare case of MYH9 disorders presenting with macrothrombocytopenia and deafness caused by MYH9-R702C mutation.

Kodama R, Taketani T, Kunishima S, Mishima S, Yoshikawa Y, Kanai R, Suyama T, Yoshino I, Kunishi H, Shibata H, Nagai A, Yamaguchi S, Masuda J.

Thromb Res. 2009 Sep;124(4):508-11. doi: 10.1016/j.thromres.2009.02.001. Epub 2009 Feb 27. No abstract available.

PMID:
19250658
18.

[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
19.

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.

J Am Soc Nephrol. 2002 Jan;13(1):65-74.

20.

[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

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