172 related articles for article (PubMed ID: 25394719)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. An interesting case of thrombocytopenia in pregnancy.
Garcia-Horton A; Chin-Yee I; Lam S
Int J Hematol; 2020 Aug; 112(2):139-140. PubMed ID: 32557127
[No Abstract] [Full Text] [Related]
7. MYH9 gene mutations associated with bleeding.
Savoia A; De Rocco D; Pecci A
Platelets; 2017 May; 28(3):312-315. PubMed ID: 28368695
[No Abstract] [Full Text] [Related]
8. 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]
9. Misdiagnosed MYH9 related inherited macrothrombocytopenia with an inadvertent splenectomy.
Thakral B; Rojanapremsuk T; Saluja K; Eldibany M
Pathology; 2015 Jun; 47(4):377-9. PubMed ID: 25938358
[No Abstract] [Full Text] [Related]
10. The case ∣ proteinuria and low platelet count.
Piccoli GB; Vigotti FN; Balduini CL; Pecci A
Kidney Int; 2012 May; 81(9):927-8. PubMed ID: 22499142
[No Abstract] [Full Text] [Related]
11. 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]
12. 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]
13. [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]
14. Macrothrombocytopenia With Döhle Body-Like Granulocyte Inclusions: A Case Report of May-Hegglin Anomaly in a 33-Year-Old White Woman With an Update on the Molecular Findings of MYH9-Related Disease.
Ruhoy SM; Yates A
Lab Med; 2016 Aug; 47(3):246-50. PubMed ID: 27353381
[TBL] [Abstract][Full Text] [Related]
15. R705H mutation of MYH9 is associated with MYH9-related disease and not only with non-syndromic deafness DFNA17.
Verver E; Pecci A; De Rocco D; Ryhänen S; Barozzi S; Kunst H; Topsakal V; Savoia A
Clin Genet; 2015 Jul; 88(1):85-9. PubMed ID: 24890873
[TBL] [Abstract][Full Text] [Related]
16. Intriguing outcome of JAK2V617F mutation seen in a patient with MYH9-related hereditary macrothrombocytopenia.
Fabris F; Scandellari R; Vettore S; Scapin M; Bizzaro N; Randi ML
Thromb Haemost; 2010 Oct; 104(4):858-9. PubMed ID: 20694274
[No Abstract] [Full Text] [Related]
17. 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]
18. 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]
19. Congenital thrombocytopenia with nephritis - The first case of MYH9 related disorder in Serbia.
Kuzmanović M; Kunishima S; Putnik J; Stajić N; Paripović A; Bogdanović R
Vojnosanit Pregl; 2014 Apr; 71(4):395-8. PubMed ID: 24783421
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]