181 related articles for article (PubMed ID: 31243205)
1. Renin-angiotensin System Blockade Therapy for Early Renal Involvement in MYH9-related Disease with an E1841K Mutation.
Tanaka M; Miki S; Saita H; Shimada H; Nishikawa S; Taniguchi K; Hagihara K; Iwanari S; Ikeda M; Kunishima S; Takeoka H
Intern Med; 2019 Oct; 58(20):2983-2988. PubMed ID: 31243205
[TBL] [Abstract][Full Text] [Related]
2. Renin-angiotensin system blockade is effective in reducing proteinuria of patients with progressive nephropathy caused by MYH9 mutations (Fechtner-Epstein syndrome).
Pecci A; Granata A; Fiore CE; Balduini CL
Nephrol Dial Transplant; 2008 Aug; 23(8):2690-2. PubMed ID: 18503011
[No Abstract] [Full Text] [Related]
3. Nonmuscle Myosin Heavy Chain IIA Mutation Predicts Severity and Progression of Sensorineural Hearing Loss in Patients With MYH9-Related Disease.
Verver EJ; Topsakal V; Kunst HP; Huygen PL; Heller PG; Pujol-Moix N; Savoia A; Benazzo M; Fierro T; Grolman W; Gresele P; Pecci A
Ear Hear; 2016; 37(1):112-20. PubMed ID: 26226608
[TBL] [Abstract][Full Text] [Related]
4.
Cechova S; Dong F; Chan F; Kelley MJ; Ruiz P; Le TH
J Am Soc Nephrol; 2018 Jan; 29(1):155-167. PubMed ID: 28993503
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. Macrothrombocytopenia, renal dysfunction and nephrotic syndrome in a young male patient: a case report of MYH9-related disease.
Sevignani G; Pavanelli GM; Milano SS; Ferronato BR; Pachaly MA; Ii Cheong H; Carvalho M; Barreto FC
J Bras Nefrol; 2018; 40(2):198-200. PubMed ID: 29782633
[TBL] [Abstract][Full Text] [Related]
8. Patients with Epstein-Fechtner syndromes owing to MYH9 R702 mutations develop progressive proteinuric renal disease.
Sekine T; Konno M; Sasaki S; Moritani S; Miura T; Wong WS; Nishio H; Nishiguchi T; Ohuchi MY; Tsuchiya S; Matsuyama T; Kanegane H; Ida K; Miura K; Harita Y; Hattori M; Horita S; Igarashi T; Saito H; Kunishima S
Kidney Int; 2010 Jul; 78(2):207-14. PubMed ID: 20200500
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. 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]
12. Clinical, pathological, and genetic analysis of ten patients with MYH9-related disease.
Sun XH; Wang ZY; Yang HY; Cao LJ; Su J; Yu ZQ; Bai X; Ruan CG
Acta Haematol; 2013; 129(2):106-13. PubMed ID: 23207509
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Familial cases with MYH9 disorders caused by MYH9 S96L mutation.
Murayama S; Akiyama M; Namba H; Wada Y; Ida H; Kunishima S
Pediatr Int; 2013 Feb; 55(1):102-4. PubMed ID: 23409987
[TBL] [Abstract][Full Text] [Related]
16. A De Novo Mutation in MYH9 in a Child With Severe and Prolonged Macrothrombocytopenia.
Li K; Jin R; Xu W; Shen Y; Lu K; Wu X
J Pediatr Hematol Oncol; 2021 Jan; 43(1):e7-e10. PubMed ID: 32520844
[TBL] [Abstract][Full Text] [Related]
17. [Clinical features and MYH9 gene variant in two Chinese siblings with Fechtner syndrome].
Zhao SL; Zhao F; Zhang AH; Huang SM
Zhonghua Er Ke Za Zhi; 2019 Apr; 57(4):286-290. PubMed ID: 30934202
[No Abstract] [Full Text] [Related]
18. 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]
19. [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]
20. A notable case report of May-Hegglin anomaly with immune complex-related nephropathy: a genetic and histological analysis.
Ohtsuka Y; Kanaji T; Nishi M; Sakai N; Sato T; Aoki S; Wakayama K; Nakazato S; Hisano S; Sado Y; Kawachi H; Izuhara K; Hamasaki Y
Clin Nephrol; 2011 Mar; 75(3):255-62. PubMed ID: 21329637
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
