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3. 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]
4. [May-Hegglin anomaly: past and present--novel diagnostic test and new concept of the disease]. Kunishima S Rinsho Byori; 2009 Jan; 57(1):54-9. PubMed ID: 19227191 [TBL] [Abstract][Full Text] [Related]
5. Mutations responsible for MYH9-related thrombocytopenia impair SDF-1-driven migration of megakaryoblastic cells. Pecci A; Bozzi V; Panza E; Barozzi S; Gruppi C; Seri M; Balduini CL Thromb Haemost; 2011 Oct; 106(4):693-704. PubMed ID: 21833445 [TBL] [Abstract][Full Text] [Related]
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7. Analysis of clinical manifestations, mutant gene and encoded protein in two Chinese MYH9-related disease families. Yi Y; Sen Zhang G; Xu M; San Ling Z; Ru Shao X; Zeng Li J; Ma J Clin Chim Acta; 2006 Nov; 373(1-2):49-54. PubMed ID: 16806139 [TBL] [Abstract][Full Text] [Related]
8. Cloning of the murine non-muscle myosin heavy chain IIA gene ortholog of human MYH9 responsible for May-Hegglin, Sebastian, Fechtner, and Epstein syndromes. D'Apolito M; Guarnieri V; Boncristiano M; Zelante L; Savoia A Gene; 2002 Mar; 286(2):215-22. PubMed ID: 11943476 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. Genetics, clinical and pathological features of glomerulonephritis associated with mutations of nonmuscle myosin IIA (Fechtner syndrome). Ghiggeri GM; Caridi G; Magrini U; Sessa A; Savoia A; Seri M; Pecci A; Romagnoli R; Gangarossa S; Noris P; Sartore S; Necchi V; Ravazzolo R; Balduini CL Am J Kidney Dis; 2003 Jan; 41(1):95-104. PubMed ID: 12500226 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. 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]
14. Identification of the first in cis mutations in MYH9 disorder. Miyajima Y; Kunishima S Eur J Haematol; 2009 Apr; 82(4):288-91. PubMed ID: 19191864 [TBL] [Abstract][Full Text] [Related]
15. Immunocytochemistry for the heavy chain of the non-muscle myosin IIA as a diagnostic tool for MYH9-related disorders. Pecci A; Noris P; Invernizzi R; Savoia A; Seri M; Ghiggeri GM; Sartore S; Gangarossa S; Bizzaro N; Balduini CL Br J Haematol; 2002 Apr; 117(1):164-7. PubMed ID: 11918549 [TBL] [Abstract][Full Text] [Related]
16. [Autosomal dominant macrothrombocytopenia with leukocyte inclusion bodies and MYH9 disorders]. Kunishima S Rinsho Byori; 2009 Apr; 57(4):365-70. PubMed ID: 19489439 [TBL] [Abstract][Full Text] [Related]