127 related articles for article (PubMed ID: 22821427)
1. 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]
2. Mutations in MYH9 exons 1, 16, 26, and 30 are infrequently found in Japanese patients with nonsyndromic deafness.
Kunishima S; Matsunaga T; Ito Y; Saito H
Genet Test Mol Biomarkers; 2009 Oct; 13(5):705-7. PubMed ID: 19645626
[TBL] [Abstract][Full Text] [Related]
3. MYH9-related disease: five novel mutations expanding the spectrum of causative mutations and confirming genotype/phenotype correlations.
De Rocco D; Zieger B; Platokouki H; Heller PG; Pastore A; Bottega R; Noris P; Barozzi S; Glembotsky AC; Pergantou H; Balduini CL; Savoia A; Pecci A
Eur J Med Genet; 2013 Jan; 56(1):7-12. PubMed ID: 23123319
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. [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]
6. G to T transversion at the first nucleotide of exon 26 of the MYH9 gene results in a novel missense mutation and abnormal splicing in platelets: comment on "A G to C transversion at the last nucleotide of exon 25 of the MYH9 gene results in a missense mutation rather than in a splicing defecton" by Vettore et al.
Kunishima S; Tomii T; Kudo K; Saito H
Eur J Med Genet; 2012 Dec; 55(12):763-5. PubMed ID: 22982478
[No Abstract] [Full Text] [Related]
7. [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]
8. [MYH9-related macrothrombocytopenia].
Nivet T; Gobert D; Mekinian A; Bibi-Triki T; Fain O
Rev Prat; 2014 Jun; 64(6):758. PubMed ID: 25090750
[No Abstract] [Full Text] [Related]
9. Advances in the understanding of MYH9 disorders.
Kunishima S; Saito H
Curr Opin Hematol; 2010 Sep; 17(5):405-10. PubMed ID: 20601875
[TBL] [Abstract][Full Text] [Related]
10. Apparent genotype-phenotype mismatch in a patient with MYH9-related disease: when the exception proves the rule.
Gresele P; De Rocco D; Bury L; Fierro T; Mezzasoma AM; Pecci A; Savoia A
Thromb Haemost; 2013 Sep; 110(3):618-20. PubMed ID: 23925420
[No Abstract] [Full Text] [Related]
11. Macrothrombocytopenia With Congenital Bilateral Cataracts: A Phenotype of MYH9 Disorder With Exon 24 Indel Mutations.
Aoki T; Kunishima S; Yamashita Y; Minamitani K; Ota S
J Pediatr Hematol Oncol; 2018 Jan; 40(1):76-78. PubMed ID: 29200148
[TBL] [Abstract][Full Text] [Related]
12. Somatic mosaicism in MYH9 disorders: the need to carefully evaluate apparently healthy parents.
Kunishima S; Kitamura K; Matsumoto T; Sekine T; Saito H
Br J Haematol; 2014 Jun; 165(6):885-7. PubMed ID: 24611568
[No Abstract] [Full Text] [Related]
13. 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]
14. 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]
15. Description of a novel mutation leading to MYH9-related disease.
Burt RA; Joseph JE; Milliken S; Collinge JE; Kile BT
Thromb Res; 2008; 122(6):861-3. PubMed ID: 18676005
[No Abstract] [Full Text] [Related]
16. 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]
17. 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]
18. A novel MYH9 mutation in a patient with MYH9 disorders and platelet size-specific effect of romiplostim on macrothrombocytopenia.
Yamanouchi J; Hato T; Kunishima S; Niiya T; Nakamura H; Yasukawa M
Ann Hematol; 2015 Sep; 94(9):1599-600. PubMed ID: 26051904
[No Abstract] [Full Text] [Related]
19. Hematologic and genetic characterization of an MYH9-related disorder in a Chinese family.
Ma ES; Wong CL; Shek TW; Hui SP
Haematologica; 2006 Jul; 91(7):1002-3. PubMed ID: 16818291
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
