96 related articles for article (PubMed ID: 22211851)
21. [The MYH9 syndrome: report of a new case with a new mutation of the MYH9 gene].
Schleinitz N; Favier R; Mazodier K; Difeo A; Ebbo M; Veit V; Berda-Haddad Y; Bernit E; Heudier P; Kaplanski G; Camoin L; Bardet V; Harle JR
Rev Med Interne; 2006 Oct; 27(10):783-6. PubMed ID: 16978745
[TBL] [Abstract][Full Text] [Related]
22. Identification and characterization of the first large deletion of the MYH9 gene associated with MYH9 disorders.
Kunishima S; Matsushita T; Hamaguchi M; Saito H
Eur J Haematol; 2008 Jun; 80(6):540-4. PubMed ID: 18284620
[TBL] [Abstract][Full Text] [Related]
23. Genotype-phenotype Correlation of the p.R1165C Mutation in the MYH9 Disorder: Report of a Japanese Pedigree.
Okano S; Takase M; Iseki K; Toriumi N; Kaneda M; Kunishima S
J Pediatr Hematol Oncol; 2015 Aug; 37(6):e352-5. PubMed ID: 26056797
[TBL] [Abstract][Full Text] [Related]
24. Adams-Oliver syndrome and familial MYH9 mutation.
Uyeda T; Echizenya T; Eto S; Ohtani K; Sato T; Takahashi T; Ito E; Yonesaka S; Kunishima S
Pediatr Int; 2012 Jun; 54(3):407-9. PubMed ID: 22631568
[No Abstract] [Full Text] [Related]
25. [MYH9 syndrome and auto-immune haemolytic anaemia: an unrelated association?].
Chauffrey L; Chamouni P; Bégarin L; Benhamou Y; Cailleux N; Borg JY; Callat MP; Schlegel N; Lévesque H
Rev Med Interne; 2012 Feb; 33(2):99-102. PubMed ID: 22217922
[TBL] [Abstract][Full Text] [Related]
26. Novel variant of
Lian X; Wang Y; Gao J; Liu H; Hao J; Kunishima S
Clin Chem Lab Med; 2021 Sep; 59(10):e398-e400. PubMed ID: 34013674
[No Abstract] [Full Text] [Related]
27. 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]
28. A rare case of MYH9 disorders presenting with macrothrombocytopenia and deafness caused by MYH9-R702C mutation.
Kodama R; Taketani T; Kunishima S; Mishima S; Yoshikawa Y; Kanai R; Suyama T; Yoshino I; Kunishi H; Shibata H; Nagai A; Yamaguchi S; Masuda J
Thromb Res; 2009 Sep; 124(4):508-11. PubMed ID: 19250658
[No Abstract] [Full Text] [Related]
29. Double nucleotidic mutation of the MYH9 gene in a young patient with end-stage renal disease.
Capria M; Andreucci M; Fuiano L; Mancuso D; Cianfrone P; Comi N; Mazza G; Caglioti A; Fuiano G
Nephrol Dial Transplant; 2004 Jan; 19(1):249-51. PubMed ID: 14671068
[No Abstract] [Full Text] [Related]
30. Identification of the first duplication in MYH9-related disease: a hot spot for unequal crossing-over within exon 24 of the MYH9 gene.
De Rocco D; Pujol-Moix N; Pecci A; Faletra F; Bozzi V; Balduini CL; Savoia A
Eur J Med Genet; 2009; 52(4):191-4. PubMed ID: 19450438
[TBL] [Abstract][Full Text] [Related]
31. Detection of unique neutrophil non-muscle myosin heavy chain-A localization by immunofluorescence analysis in MYH9 disorder presented with macrothrombocytopenia without leukocyte inclusions and deafness.
Kunishima S; Matsushita T; Shiratsuchi M; Ikuta T; Nishimura J; Hamaguchi M; Naoe T; Saito H
Eur J Haematol; 2005 Jan; 74(1):1-5. PubMed ID: 15613099
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. Giant platelet syndromes and the MYH9 mutations.
Balduini CL
Lab Hematol; 2004; 10(3):187-8. PubMed ID: 15529446
[No Abstract] [Full Text] [Related]
34. A family with Bolzano-type Bernard-Soulier syndrome carries a benign A1939T MYH9 mutation.
Sarangi SN; Golightly M; Weber J; Chan EL
Platelets; 2013; 24(1):81-4. PubMed ID: 22372535
[No Abstract] [Full Text] [Related]
35. Non-muscle myosin heavy chain IIA and IIB interact and co-localize in living cells: relevance for MYH9-related disease.
Marini M; Bruschi M; Pecci A; Romagnoli R; Musante L; Candiano G; Ghiggeri GM; Balduini C; Seri M; Ravazzolo R
Int J Mol Med; 2006 May; 17(5):729-36. PubMed ID: 16596254
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. Transient hemiparesis in a 14-year-old boy with MYH9 disorders.
Kitamura K; Kunishima S; Tahara M; Ogiwara S; Dobata N; Dobata T; Sugihara A; Nakashima T; Sasaki Y; Nagumo K; Kubota M; Kinugawa Y; Ieko M; Kumaki S
Int J Hematol; 2012 Sep; 96(3):376-9. PubMed ID: 22821427
[No Abstract] [Full Text] [Related]
38. Thrombocytopenia and proteinuria. Nonmuscle myosin heavy-chain-9-related disease ( MYH9 RD) or Epstein syndrome (ES).
Bhatt A; Broxson E; Witte D; Omoloja A
Pediatr Nephrol; 2009 Mar; 24(3):485-8. PubMed ID: 18781340
[No Abstract] [Full Text] [Related]
39. Megakaryocytes of patients with MYH9-related thrombocytopenia present an altered proplatelet formation.
Pecci A; Malara A; Badalucco S; Bozzi V; Torti M; Balduini CL; Balduini A
Thromb Haemost; 2009 Jul; 102(1):90-6. PubMed ID: 19572073
[TBL] [Abstract][Full Text] [Related]
40. Germinal mosaicism in MYH9 disorders: a family with two affected siblings of normal parents.
Kunishima S; Takaki K; Ito Y; Saito H
Br J Haematol; 2009 Apr; 145(2):260-2. PubMed ID: 19208103
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
