202 related articles for article (PubMed ID: 26861218)
1. 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]
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. MYH9-related disease: description of a large Chinese pedigree and a survey of reported mutations.
Zhang S; Zhou X; Liu S; Bai T; Zhang Y; Wang J; Wang S; Zhang X; Wang B
Acta Haematol; 2014; 132(2):193-8. PubMed ID: 24643058
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Genotype-phenotype correlation of a novel MYH9 mutation (p.G736L) in a patient with macrothrombocytopenia and end-stage renal disease.
Souto Filho JTD; Lemos MM; Piraciaba JCB; Silveira ALO; Lacerda AP; Pires AZ; de Sales LR; Dias YP
Ann Hematol; 2019 Mar; 98(3):781-782. PubMed ID: 30617524
[No Abstract] [Full Text] [Related]
6. 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]
7. 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]
8. 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]
9. 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]
10. 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]
11. 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]
12. 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]
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. 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]
15. 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]
16. MYH9-Related Thrombocytopenia: Four Novel Variants Affecting the Tail Domain of the Non-Muscle Myosin Heavy Chain IIA Associated with a Mild Clinical Evolution of the Disorder.
Zaninetti C; De Rocco D; Giangregorio T; Bozzi V; Demeter J; Leoni P; Noris P; Ryhänen S; Barozzi S; Pecci A; Savoia A
Hamostaseologie; 2019 Feb; 39(1):87-94. PubMed ID: 29996171
[TBL] [Abstract][Full Text] [Related]
17. [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]
18. Macrothrombocytopenia and progressive deafness is due to a mutation in MYH9.
Mhatre AN; Kim Y; Brodie HA; Lalwani AK
Otol Neurotol; 2003 Mar; 24(2):205-9. PubMed ID: 12621333
[TBL] [Abstract][Full Text] [Related]
19. A D1424N mutation in the MYH9 gene results in macrothrombocytopenia and granulocytic inclusion bodies in a Chinese inherited macrothrombocytopenia pedigree.
Guo X; Lian X; Zhang W; Hao J
Clin Chem Lab Med; 2018 Jun; 56(7):e171-e173. PubMed ID: 29451856
[No 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]
