Kunishima S - Search Results

1

Novel biallelic GNE variants identified in a patient with chronic thrombocytopenia without any symptoms of myopathy.

Tsuda S, Sakamoto A, Kawaguchi H, Uchiyama T, Kaname T, Yanagi K, Kunishima S, Ishiguro A. Tsuda S, et al. Among authors: kunishima s. Ann Hematol. 2024 Dec;103(12):5945-5950. doi: 10.1007/s00277-024-06104-0. Epub 2024 Nov 22. Ann Hematol. 2024. PMID: 39576359

2

Splenectomy as an effective treatment for macrothrombocytopenia in Takenouchi-Kosaki syndrome.

Yamano S, Iguchi A, Ishikawa K, Sakamoto A, Uchiyama T, Yanagi K, Kaname T, Kunishima S, Ishiguro A. Yamano S, et al. Among authors: kunishima s. Int J Hematol. 2023 Apr;117(4):622-625. doi: 10.1007/s12185-022-03491-w. Epub 2022 Dec 2. Int J Hematol. 2023. PMID: 36459360

3

[Developments of high-throughput sequencing-based diagnosis of congenital thrombocytopenia/platelet disorders in a registry study].

Ishiguro A, Uchiyama T, Sakamoto A, Kunishima S. Ishiguro A, et al. Among authors: kunishima s. Rinsho Ketsueki. 2024;65(8):747-755. doi: 10.11406/rinketsu.65.747. Rinsho Ketsueki. 2024. PMID: 39231703 Japanese.

4

Bernard-Soulier syndrome caused by a novel GP1BB variant and 22q11.2 deletion.

Nagoshi R, Sakamoto A, Imai T, Uchiyama T, Kaname T, Kunishima S, Ishiguro A. Nagoshi R, et al. Among authors: kunishima s. Int J Hematol. 2024 Jul;120(1):142-145. doi: 10.1007/s12185-024-03768-2. Epub 2024 Apr 16. Int J Hematol. 2024. PMID: 38625506

5

Diagnostic delay of MYH9-related disorder in Japan.

Sakamoto A, Uchiyama T, Kaname T, Iguchi A, Ohara O, Ishimura M, Onum M, Kunishima S, Ishiguro A. Sakamoto A, et al. Among authors: kunishima s. Br J Haematol. 2024 Jun;204(6):2400-2404. doi: 10.1111/bjh.19484. Epub 2024 Apr 22. Br J Haematol. 2024. PMID: 38650331

6

Platelet changes and bleeding symptoms in children, adolescents, and adults with 22q11.2 deletion syndrome.

Sakamoto A, Uchiyama T, Futatsugi R, Ohara O, Iguchi A, Kaname T, Hikosaka M, Ono H, Kunishima S, Ito S, Ishiguro A. Sakamoto A, et al. Among authors: kunishima s. Pediatr Blood Cancer. 2024 Nov;71(11):e31292. doi: 10.1002/pbc.31292. Epub 2024 Sep 3. Pediatr Blood Cancer. 2024. PMID: 39228058

7

Case Report: MYH9-related disease caused by Ala44Pro mutation in a child with a previous diagnosis of chronic immune thrombocytopenia.

Niwa K, Toyoda H, Kohso A, Okumura Y, Kunishima S, Hirayama M. Niwa K, et al. Among authors: kunishima s. Front Pediatr. 2024 May 17;12:1391742. doi: 10.3389/fped.2024.1391742. eCollection 2024. Front Pediatr. 2024. PMID: 38827217 Free PMC article.

8

MYH9-related disease with a normal platelet count.

Nakatani R, Miura K, Shirai Y, Taneda S, Horinouchi T, Nozu K, Honda K, Yamaguchi Y, Kunishima S, Hattori M. Nakatani R, et al. Among authors: kunishima s. CEN Case Rep. 2024 Aug 3. doi: 10.1007/s13730-024-00922-x. Online ahead of print. CEN Case Rep. 2024. PMID: 39096414 Free article.

9

Successful administration of eltrombopag in preparation for peritoneal dialysis catheter placement in a girl with MYH9-related disease.

Nakamura M, Miura K, Shirai Y, Ishizuka K, Nakamura T, Segawa O, Kunishima S, Hattori M. Nakamura M, et al. Among authors: kunishima s. CEN Case Rep. 2023 Nov;12(4):419-422. doi: 10.1007/s13730-023-00786-7. Epub 2023 Mar 31. CEN Case Rep. 2023. PMID: 37000325 Free PMC article.

10

A nationwide survey of MYH9-related disease in Japan.

Shirai Y, Miura K, Hamada R, Ishikura K, Kunishima S, Hattori M. Shirai Y, et al. Among authors: kunishima s. Clin Exp Nephrol. 2024 Jan;28(1):40-49. doi: 10.1007/s10157-023-02404-3. Epub 2023 Sep 21. Clin Exp Nephrol. 2024. PMID: 37733142

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