Kunishima S - Search Results

1

Two Cases of the MYH9 Disorder Fechtner Syndrome Diagnosed from Observation of Peripheral Blood Cells before End-Stage Renal Failure.

Teshirogi S, Muratsu J, Kasahara H, Terashima K, Miki S, Minami T, Okute Y, Yoneda S, Morishima A, Kunishima S, Sakaguchi K. Teshirogi S, et al. Among authors: kunishima s. Case Rep Nephrol. 2019 Nov 26;2019:5149762. doi: 10.1155/2019/5149762. eCollection 2019. Case Rep Nephrol. 2019. PMID: 31885961 Free PMC article.

2

Perinatal Management for a Pregnant Woman with an MYH9 Disorder.

Yamashita Y, Matsuura R, Kunishima S, Oikawa Y, Ariizumi H, Hamada S, Shirato N, Matsuoka R, Ogawa K, Sekizawa A. Yamashita Y, et al. Among authors: kunishima s. Case Rep Obstet Gynecol. 2016;2016:6730174. doi: 10.1155/2016/6730174. Epub 2016 Jun 29. Case Rep Obstet Gynecol. 2016. PMID: 27437156 Free PMC article.

3

Renin-angiotensin System Blockade Therapy for Early Renal Involvement in MYH9-related Disease with an E1841K Mutation.

Tanaka M, Miki S, Saita H, Shimada H, Nishikawa S, Taniguchi K, Hagihara K, Iwanari S, Ikeda M, Kunishima S, Takeoka H. Tanaka M, et al. Among authors: kunishima s. Intern Med. 2019 Oct 15;58(20):2983-2988. doi: 10.2169/internalmedicine.2997-19. Epub 2019 Jun 27. Intern Med. 2019. PMID: 31243205 Free PMC article.

4

Advances in the understanding of MYH9 disorders.

Kunishima S, Saito H. Kunishima S, et al. Curr Opin Hematol. 2010 Sep;17(5):405-10. doi: 10.1097/MOH.0b013e32833c069c. Curr Opin Hematol. 2010. PMID: 20601875 Review.

5

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. Okano S, et al. Among authors: kunishima s. J Pediatr Hematol Oncol. 2015 Aug;37(6):e352-5. doi: 10.1097/MPH.0000000000000379. J Pediatr Hematol Oncol. 2015. PMID: 26056797

6

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. Makino S, et al. Among authors: kunishima s. Pediatr Int. 2015 Oct;57(5):977-81. doi: 10.1111/ped.12736. Epub 2015 Sep 21. Pediatr Int. 2015. PMID: 26387855

7

Late onset and high-frequency dominant hearing loss in a family with MYH9 disorder.

Wasano K, Matsunaga T, Ogawa K, Kunishima S. Wasano K, et al. Among authors: kunishima s. Eur Arch Otorhinolaryngol. 2016 Nov;273(11):3547-3552. doi: 10.1007/s00405-016-3954-0. Epub 2016 Mar 4. Eur Arch Otorhinolaryngol. 2016. PMID: 26942920

8

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. Aoki T, et al. Among authors: kunishima s. J Pediatr Hematol Oncol. 2018 Jan;40(1):76-78. doi: 10.1097/MPH.0000000000000998. J Pediatr Hematol Oncol. 2018. PMID: 29200148

9

11q23 deletion syndrome (Jacobsen syndrome) with severe bleeding: a case report.

Ichimiya Y, Wada Y, Kunishima S, Tsukamoto K, Kosaki R, Sago H, Ishiguro A, Ito Y. Ichimiya Y, et al. Among authors: kunishima s. J Med Case Rep. 2018 Jan 8;12(1):3. doi: 10.1186/s13256-017-1535-5. J Med Case Rep. 2018. PMID: 29307309 Free PMC article.

10

Identification of six novel MYH9 mutations and genotype-phenotype relationships in autosomal dominant macrothrombocytopenia with leukocyte inclusions.

Kunishima S, Matsushita T, Kojima T, Amemiya N, Choi YM, Hosaka N, Inoue M, Jung Y, Mamiya S, Matsumoto K, Miyajima Y, Zhang G, Ruan C, Saito K, Song KS, Yoon HJ, Kamiya T, Saito H. Kunishima S, et al. J Hum Genet. 2001;46(12):722-9. doi: 10.1007/s100380170007. J Hum Genet. 2001. PMID: 11776386

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