308 related articles for article (PubMed ID: 23409987)
21. Hereditary thrombocytopenia with familial novel mutation in MYH9 gene: A familial case report.
Ciftciler R; Balasar Ö; Keyik H; Ciftciler AE
Transfus Apher Sci; 2023 Aug; 62(4):103710. PubMed ID: 37076359
[TBL] [Abstract][Full Text] [Related]
22. [Hereditary sensorineural hearing impairment and macrothrombocytopenia: a rare MYH9 gene mutation].
Böttcher A; Knecht R; Busch CJ; Lörincz BB; Dalchow CV
HNO; 2013 Feb; 61(2):159-60, 162-5. PubMed ID: 23223919
[TBL] [Abstract][Full Text] [Related]
23. MYH9 Associated nephropathy.
Furlano M; Arlandis R; Venegas MDP; Novelli S; Crespi J; Bullich G; Ayasreh N; Remacha Á; Ruiz P; Lorente L; Ballarín J; Matamala A; Ars E; Torra R
Nefrologia (Engl Ed); 2019; 39(2):133-140. PubMed ID: 30471777
[TBL] [Abstract][Full Text] [Related]
24. Avatrombopag improves thrombocytopenia in MYH9-related disorder following eltrombopag treatment failure.
Arif AR; Zhao M; Chen W; Xue M; Luo S; Wang Y
Platelets; 2022 Nov; 33(8):1307-1311. PubMed ID: 35791514
[TBL] [Abstract][Full Text] [Related]
25. A Japanese pedigree with a p.A95V mutation in the MYH9 gene demonstrates inherited macrothrombocytopenia without Alport manifestations.
Yokoi S; Kunishima S; Takahashi Y; Morishita M; Kojima S
Ann Hematol; 2016 Apr; 95(5):831-3. PubMed ID: 26861218
[No Abstract] [Full Text] [Related]
26. The first two cases of MYH9 disorders in Thailand: an international collaborative study.
Sirachainan N; Komwilaisak P; Kitamura K; Hongeng S; Sekine T; Kunishima S
Ann Hematol; 2015 Apr; 94(4):707-9. PubMed ID: 25394719
[No Abstract] [Full Text] [Related]
27. Haematological characteristics of MYH9 disorders due to MYH9 R702 mutations.
Kunishima S; Yoshinari M; Nishio H; Ida K; Miura T; Matsushita T; Hamaguchi M; Saito H
Eur J Haematol; 2007 Mar; 78(3):220-6. PubMed ID: 17241369
[TBL] [Abstract][Full Text] [Related]
28. Genotype-phenotype correlation of a novel MYH9 mutation (p.G736L) in a patient with macrothrombocytopenia and end-stage renal disease.
Souto Filho JTD; Lemos MM; Piraciaba JCB; Silveira ALO; Lacerda AP; Pires AZ; de Sales LR; Dias YP
Ann Hematol; 2019 Mar; 98(3):781-782. PubMed ID: 30617524
[No Abstract] [Full Text] [Related]
29. Management of patients with severe Epstein syndrome: Review of four patients who received living-donor renal transplantation.
Hashimoto J; Hamasaki Y; Takahashi Y; Kubota M; Yanagisawa T; Itabashi Y; Muramatsu M; Kawamura T; Kumagai N; Ohwada Y; Sakai K; Shishido S
Nephrology (Carlton); 2019 Apr; 24(4):450-455. PubMed ID: 29532554
[TBL] [Abstract][Full Text] [Related]
30. Renal manifestations of patients with MYH9-related disorders.
Han KH; Lee H; Kang HG; Moon KC; Lee JH; Park YS; Ha IS; Ahn HS; Choi Y; Cheong HI
Pediatr Nephrol; 2011 Apr; 26(4):549-55. PubMed ID: 21210153
[TBL] [Abstract][Full Text] [Related]
31. 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. PubMed ID: 23007341
[TBL] [Abstract][Full Text] [Related]
32. [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 Yi Xue Ban; 2008 Apr; 40(2):160-4. PubMed ID: 18458691
[TBL] [Abstract][Full Text] [Related]
33. MYH9 related platelet disorders - often unknown and misdiagnosed.
Althaus K; Najm J; Greinacher A
Klin Padiatr; 2011 May; 223(3):120-5. PubMed ID: 21567368
[TBL] [Abstract][Full Text] [Related]
34. [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. PubMed ID: 21429376
[TBL] [Abstract][Full Text] [Related]
35. 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. PubMed ID: 26446054
[TBL] [Abstract][Full Text] [Related]
36. A novel de novo MYH9 mutation in MYH9-related disease: A case report and review of literature.
Ai Q; Zhao L; Yin J; Jiang L; Jin Q; Hu X; Chen S
Medicine (Baltimore); 2020 Jan; 99(4):e18887. PubMed ID: 31977897
[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. MYH9-related disease: a novel prognostic model to predict the clinical evolution of the disease based on genotype-phenotype correlations.
Pecci A; Klersy C; Gresele P; Lee KJ; De Rocco D; Bozzi V; Russo G; Heller PG; Loffredo G; Ballmaier M; Fabris F; Beggiato E; Kahr WH; Pujol-Moix N; Platokouki H; Van Geet C; Noris P; Yerram P; Hermans C; Gerber B; Economou M; De Groot M; Zieger B; De Candia E; Fraticelli V; Kersseboom R; Piccoli GB; Zimmermann S; Fierro T; Glembotsky AC; Vianello F; Zaninetti C; Nicchia E; Güthner C; Baronci C; Seri M; Knight PJ; Balduini CL; Savoia A
Hum Mutat; 2014 Feb; 35(2):236-47. PubMed ID: 24186861
[TBL] [Abstract][Full Text] [Related]
39. 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]
40. [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]
[Previous] [Next] [New Search]