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Items: 1 to 20 of 31

1.

[Renal diseases related to MYH9 disorders].

Galeano D, Zanoli L, L'Imperio V, Fatuzzo P, Granata A.

G Ital Nefrol. 2017 Apr;34(2):40-57. Review. Italian.

PMID:
28682562
2.

[Which genetic testing in renal disease].

Granata M, Canto C, Mazzarino MC, Fatuzzo P, Granata A.

G Ital Nefrol. 2015 Sep-Oct;32(5). pii: gin/32.5.3. Review. Italian.

PMID:
26480254
3.

Preoperative use of platelets in a 6-year-old with acute appendicitis and a myosin heavy chain 9-related disorder: a case report and review of literature.

Eichel Y, Tormos LM, Squires JE.

Transfusion. 2016 Feb;56(2):349-53. doi: 10.1111/trf.13366. Epub 2015 Oct 7. Review.

PMID:
26446054
4.

MYH9-related thrombocytopenia and intracranial bleedings: a complex clinical/surgical management and review of the literature.

Palandri F, Zoli M, Polverelli N, Noris P, Sollazzo D, Catani L, Vianelli N, Palandri G.

Br J Haematol. 2015 Sep;170(5):729-31. doi: 10.1111/bjh.13324. Epub 2015 Mar 8. Review. No abstract available. Erratum in: Br J Haematol. 2016 Jan;172(1):147.

PMID:
25752999
5.

[Recent progress in platelet laboratory testing].

Yatomi Y.

Rinsho Ketsueki. 2014 Oct;55(10):2054-9. Review. Japanese. No abstract available.

PMID:
25297771
6.

[Anaesthetic implications in a pregnant patient with an extreme thrombocytopenia due to a May-Hegglin anomaly: general o regional anaesthesia?].

GarcĂ­a Vallejo G, Cabellos M, Kabiri M, Fraile JR, Cuesta J.

Rev Esp Anestesiol Reanim. 2014 Oct;61(8):460-5. doi: 10.1016/j.redar.2014.02.006. Epub 2014 Apr 4. Review. Spanish.

PMID:
24704095
7.

MYH9-related disease: description of a large Chinese pedigree and a survey of reported mutations.

Zhang S, Zhou X, Liu S, Bai T, Zhang Y, Wang J, Wang S, Zhang X, Wang B.

Acta Haematol. 2014;132(2):193-8. Review.

PMID:
24643058
8.

May-Hegglin anomaly and pregnancy: a systematic review.

Hussein BA, Gomez K, Kadir RA.

Blood Coagul Fibrinolysis. 2013 Jul;24(5):554-61. doi: 10.1097/MBC.0b013e32835fad03. Review.

PMID:
23811802
9.

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
10.

Genetics of familial forms of thrombocytopenia.

Balduini CL, Savoia A.

Hum Genet. 2012 Dec;131(12):1821-32. doi: 10.1007/s00439-012-1215-x. Epub 2012 Aug 11. Review.

PMID:
22886561
11.

Association of a novel in-frame deletion mutation of the MYH9 gene with end-stage renal failure: case report and review of the literature.

Ishida M, Mori Y, Ota N, Inaba T, Kunishima S.

Clin Nephrol. 2013 Sep;80(3):218-22. doi: 10.5414/CN107237. Review.

PMID:
22541678
12.

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
13.

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
14.

[Fechtner syndrome, a nonmuscle myosin heavy chain 9 gene mutation related disease: a case report and literature review].

Hu R, Hao JH, Yang HL, Zhu Y, Li SY, Zhao J, Lin FR, Niu ZY.

Zhonghua Xue Ye Xue Za Zhi. 2011 Feb;32(2):103-6. Review. Chinese.

PMID:
21429376
15.

Genetic disorders of glomerular basement membranes.

Kashtan CE, Segal Y.

Nephron Clin Pract. 2011;118(1):c9-c18. doi: 10.1159/000320876. Epub 2010 Nov 11. Review.

PMID:
21071975
16.

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
17.

CKD in MYH9-related disorders.

Singh N, Nainani N, Arora P, Venuto RC.

Am J Kidney Dis. 2009 Oct;54(4):732-40. doi: 10.1053/j.ajkd.2009.06.023. Epub 2009 Sep 2. Review.

PMID:
19726116
18.

Regulation of platelet biogenesis: insights from the May-Hegglin anomaly and other MYH9-related disorders.

Chen Z, Shivdasani RA.

J Thromb Haemost. 2009 Jul;7 Suppl 1:272-6. doi: 10.1111/j.1538-7836.2009.03425.x. Review.

19.

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

Kunishima S.

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

PMID:
19489439
20.

MYH9-related platelet disorders.

Althaus K, Greinacher A.

Semin Thromb Hemost. 2009 Mar;35(2):189-203. doi: 10.1055/s-0029-1220327. Epub 2009 Apr 30. Review.

PMID:
19408192

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