Similar articles for PMID: 11776386

Year	Number of Results
1913	1
1962	1
1975	2
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1981	1
1982	2
1984	1
1985	1
1988	4
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1990	3
1991	2
1992	2
1993	4
1994	2
1995	2
1996	1
1997	5
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1999	6
2000	12
2001	6
2002	13
2003	15
2004	8
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2007	8
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2013	13
2014	12
2015	15
2016	9
2017	12
2018	14
2019	13
2020	9
2021	12
2022	6
2023	2
2024	1

1

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

2

Hereditary thrombocytopenia with familial novel mutation in MYH9 gene: A familial case report.

Ciftciler R, Balasar Ö, Keyik H, Ciftciler AE. Ciftciler R, et al. Transfus Apher Sci. 2023 Aug;62(4):103710. doi: 10.1016/j.transci.2023.103710. Epub 2023 Apr 6. Transfus Apher Sci. 2023. PMID: 37076359

3

A familial case of MYH9 gene mutation associated with multiple functional and structural platelet abnormalities.

Safiullina SI, Evtugina NG, Andrianova IA, Khismatullin RR, Kravtsova OA, Khabirova AI, Nagaswami C, Daminova AG, Peshkova AD, Litvinov RI, Weisel JW. Safiullina SI, et al. Sci Rep. 2022 Nov 20;12(1):19975. doi: 10.1038/s41598-022-24098-5. Sci Rep. 2022. PMID: 36404341 Free PMC article.

4

Avatrombopag improves thrombocytopenia in MYH9-related disorder following eltrombopag treatment failure.

Arif AR, Zhao M, Chen W, Xue M, Luo S, Wang Y. Arif AR, et al. Platelets. 2022 Nov 17;33(8):1307-1311. doi: 10.1080/09537104.2022.2096211. Epub 2022 Jul 5. Platelets. 2022. PMID: 35791514

5

Defective VWF secretion due to expression of MYH9-RD E1841K mutant in endothelial cells disrupts hemostasis.

Cao Y, Sun Y, Deng Y, Wei G, Liu J, Jin S, Dong C, Kang X, Huo Y, Zhang J, Luo J. Cao Y, et al. Blood Adv. 2022 Aug 9;6(15):4537-4552. doi: 10.1182/bloodadvances.2022008011. Blood Adv. 2022. PMID: 35764499 Free PMC article.

6

Reduced platelet forces underlie impaired hemostasis in mouse models of MYH9-related disease.

Baumann J, Sachs L, Otto O, Schoen I, Nestler P, Zaninetti C, Kenny M, Kranz R, von Eysmondt H, Rodriguez J, Schäffer TE, Nagy Z, Greinacher A, Palankar R, Bender M. Baumann J, et al. Sci Adv. 2022 May 20;8(20):eabn2627. doi: 10.1126/sciadv.abn2627. Epub 2022 May 18. Sci Adv. 2022. PMID: 35584211 Free PMC article.

7

The surgical management of a patient with chronic renal failure and macrothrombocytopenia related to the MYH9 gene mutation: A case report.

Costa RF, Bucharles SGE, Kagueiama DE, Kus CP, Andrade AA, Dirschnabel AJ, de Araujo MR, de Lima AAS. Costa RF, et al. Spec Care Dentist. 2022 Nov;42(6):651-656. doi: 10.1111/scd.12727. Epub 2022 May 10. Spec Care Dentist. 2022. PMID: 35537118

8

Ex vivo anticoagulants affect human blood platelet biomechanics with implications for high-throughput functional mechanophenotyping.

Sachs L, Wesche J, Lenkeit L, Greinacher A, Bender M, Otto O, Palankar R. Sachs L, et al. Commun Biol. 2022 Jan 21;5(1):86. doi: 10.1038/s42003-021-02982-6. Commun Biol. 2022. PMID: 35064207 Free PMC article.

9

[Clinical and genetic features of seven children with MYH9-related disease].

Hu Y, Ma JY, Liu HQ, Yang BX, Zhao SS, Zhang JL, Wu RH. Hu Y, et al. Zhonghua Er Ke Za Zhi. 2021 Nov 2;59(11):968-972. doi: 10.3760/cma.j.cn112140-20210809-00657. Zhonghua Er Ke Za Zhi. 2021. PMID: 34711033 Chinese.

10

[Gene analysis and clinical features of MYH9-related disease].

Luo XJ, Cao K, Liu J, Duan QY, Chen SY, Zhang Y, Huang T, Mao XN, Li CG, Chen YS. Luo XJ, et al. Zhonghua Er Ke Za Zhi. 2021 Nov 2;59(11):957-962. doi: 10.3760/cma.j.cn112140-20210507-00389. Zhonghua Er Ke Za Zhi. 2021. PMID: 34711031 Chinese.

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