430 related articles for article (PubMed ID: 29090586)
21. Establishment of mouse model of MYH9 disorders: heterozygous R702C mutation provokes macrothrombocytopenia with leukocyte inclusion bodies, renal glomerulosclerosis and hearing disability.
Suzuki N; Kunishima S; Ikejiri M; Maruyama S; Sone M; Takagi A; Ikawa M; Okabe M; Kojima T; Saito H; Naoe T; Matsushita T
PLoS One; 2013; 8(8):e71187. PubMed ID: 23976996
[TBL] [Abstract][Full Text] [Related]
22. [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
Zhonghua Er Ke Za Zhi; 2021 Nov; 59(11):968-972. PubMed ID: 34711033
[No Abstract] [Full Text] [Related]
23. 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. PubMed ID: 22541678
[TBL] [Abstract][Full Text] [Related]
24. MYH9-Related Thrombocytopenia: Four Novel Variants Affecting the Tail Domain of the Non-Muscle Myosin Heavy Chain IIA Associated with a Mild Clinical Evolution of the Disorder.
Zaninetti C; De Rocco D; Giangregorio T; Bozzi V; Demeter J; Leoni P; Noris P; Ryhänen S; Barozzi S; Pecci A; Savoia A
Hamostaseologie; 2019 Feb; 39(1):87-94. PubMed ID: 29996171
[TBL] [Abstract][Full Text] [Related]
25. Late onset and high-frequency dominant hearing loss in a family with MYH9 disorder.
Wasano K; Matsunaga T; Ogawa K; Kunishima S
Eur Arch Otorhinolaryngol; 2016 Nov; 273(11):3547-3552. PubMed ID: 26942920
[TBL] [Abstract][Full Text] [Related]
26. Position of nonmuscle myosin heavy chain IIA (NMMHC-IIA) mutations predicts the natural history of MYH9-related disease.
Pecci A; Panza E; Pujol-Moix N; Klersy C; Di Bari F; Bozzi V; Gresele P; Lethagen S; Fabris F; Dufour C; Granata A; Doubek M; Pecoraro C; Koivisto PA; Heller PG; Iolascon A; Alvisi P; Schwabe D; De Candia E; Rocca B; Russo U; Ramenghi U; Noris P; Seri M; Balduini CL; Savoia A
Hum Mutat; 2008 Mar; 29(3):409-17. PubMed ID: 18059020
[TBL] [Abstract][Full Text] [Related]
27. A Case of Myosin Heavy Chain 9-Related Disorder Following Splenectomy Due to Misdiagnosis of Idiopathic Thrombocytopenic Purpura.
Arslan Davulcu E; Karaca E; Akad Soyer N
Cureus; 2024 Feb; 16(2):e55064. PubMed ID: 38550428
[TBL] [Abstract][Full Text] [Related]
28. [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
Zhonghua Er Ke Za Zhi; 2021 Nov; 59(11):957-962. PubMed ID: 34711031
[No Abstract] [Full Text] [Related]
29. 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. PubMed ID: 15667538
[TBL] [Abstract][Full Text] [Related]
30. Platelet diameters in inherited thrombocytopenias: analysis of 376 patients with all known disorders.
Noris P; Biino G; Pecci A; Civaschi E; Savoia A; Seri M; Melazzini F; Loffredo G; Russo G; Bozzi V; Notarangelo LD; Gresele P; Heller PG; Pujol-Moix N; Kunishima S; Cattaneo M; Bussel J; De Candia E; Cagioni C; Ramenghi U; Barozzi S; Fabris F; Balduini CL
Blood; 2014 Aug; 124(6):e4-e10. PubMed ID: 24990887
[TBL] [Abstract][Full Text] [Related]
31. Platelet size distinguishes between inherited macrothrombocytopenias and immune thrombocytopenia.
Noris P; Klersy C; Zecca M; Arcaini L; Pecci A; Melazzini F; Terulla V; Bozzi V; Ambaglio C; Passamonti F; Locatelli F; Balduini CL
J Thromb Haemost; 2009 Dec; 7(12):2131-6. PubMed ID: 19740094
[TBL] [Abstract][Full Text] [Related]
32. A unique immunofluorescence method promotes accurate diagnosis in MYH9 disorders: a case report.
Yoshinari M; Kunishima S; Miyabayashi S; Saito H; Tsuchiya S
J Pediatr Hematol Oncol; 2004 Sep; 26(9):579-83. PubMed ID: 15342975
[TBL] [Abstract][Full Text] [Related]
33. Use of the novel thrombopoietin receptor-agonist romiplostim, in combination with steroids and immunoglobulins for the increase of platelets prior to splenectomy, in refractory immune thrombocytopenia: a case report.
Sivera P; Ruella M; Gueli A; Hu H; Wade M; Tarella C
Blood Coagul Fibrinolysis; 2012 Jun; 23(4):331-4. PubMed ID: 22343685
[TBL] [Abstract][Full Text] [Related]
34. Thrombopoietin receptor agonists in patients with persistent or chronic immune thrombocytopenia.
Agnelli Giacchello J; Valeri F; Boccadoro M; Borchiellini A
Eur J Haematol; 2018 Mar; 100(3):304-307. PubMed ID: 29243329
[TBL] [Abstract][Full Text] [Related]
35. Sporadic Epstein syndrome with macrothrombocytopenia, sensorineural hearing loss and renal failure.
Makino S; Kunishima S; Ikumi A; Awaguni H; Shinozuka J; Tanaka S; Maruyama R; Imashuku S
Pediatr Int; 2015 Oct; 57(5):977-81. PubMed ID: 26387855
[TBL] [Abstract][Full Text] [Related]
36. 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. PubMed ID: 21542825
[TBL] [Abstract][Full Text] [Related]
37. Unveiling the hidden clues: Döhle body-like inclusions as morphological markers for MYH9-related disorders: A case report.
Zhang Y; Zuo Z; Yu W; Xu A
Medicine (Baltimore); 2023 Dec; 102(51):e36735. PubMed ID: 38134071
[TBL] [Abstract][Full Text] [Related]
38. Renal Biopsy-induced Hematoma and Infection in a Patient with Asymptomatic May-Hegglin Anomaly.
Matsumoto T; Yanagihara T; Yoshizaki K; Tsuchiya M; Terasaki M; Nagahama K; Shimizu A; Kunishima S; Maeda M
J Nippon Med Sch; 2021 Dec; 88(6):579-584. PubMed ID: 33692298
[TBL] [Abstract][Full Text] [Related]
39. Successful immunostaining demonstrates abnormal intracytoplasmic MYH9 protein (NMMHC-IIA) in neutrophils of a dog with May-Hegglin anomaly.
Flatland B; Kunishima S
Vet Clin Pathol; 2011 Dec; 40(4):409-410. PubMed ID: 22136472
[No Abstract] [Full Text] [Related]
40. 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
J Hum Genet; 2001; 46(12):722-9. PubMed ID: 11776386
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]