Uchiyama T - 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: uchiyama t. 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

ETV6-related thrombocytopenia associated with a transient decrease in von Willebrand factor.

Kanamaru Y, Uchiyama T, Kaname T, Yanagi K, Ohara O, Kunishima S, Ishiguro A. Kanamaru Y, et al. Among authors: uchiyama t. Int J Hematol. 2021 Aug;114(2):297-300. doi: 10.1007/s12185-021-03136-4. Epub 2021 Mar 25. Int J Hematol. 2021. PMID: 33768492

3

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: uchiyama t. 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

4

[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: uchiyama t. Rinsho Ketsueki. 2024;65(8):747-755. doi: 10.11406/rinketsu.65.747. Rinsho Ketsueki. 2024. PMID: 39231703 Japanese.

5

Measurement of immature platelet fraction is useful in the differential diagnosis of MYH9 disorders.

Kouno H, Kunishima S, Takebe J, Uchiyama T, Kaname T, Ishiguro A. Kouno H, et al. Among authors: uchiyama t. Int J Lab Hematol. 2023 Oct;45(5):700-706. doi: 10.1111/ijlh.14123. Epub 2023 Jun 16. Int J Lab Hematol. 2023. PMID: 37328958

6

Inherited macrothrombocytopenia due to a novel splice donor site mutation in ITGB3.

Komeno Y, Uchiyama T, Kawano F, Kurihara Y, Kurokawa M, Ohara O, Kunishima S, Ishiguro A. Komeno Y, et al. Among authors: uchiyama t. Ann Hematol. 2023 Oct;102(10):2947-2949. doi: 10.1007/s00277-023-05387-z. Epub 2023 Jul 29. Ann Hematol. 2023. PMID: 37515626 No abstract available.

7

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: uchiyama t. 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

8

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: uchiyama t. Br J Haematol. 2024 Jun;204(6):2400-2404. doi: 10.1111/bjh.19484. Epub 2024 Apr 22. Br J Haematol. 2024. PMID: 38650331

9

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: uchiyama t. Pediatr Blood Cancer. 2024 Nov;71(11):e31292. doi: 10.1002/pbc.31292. Epub 2024 Sep 3. Pediatr Blood Cancer. 2024. PMID: 39228058

10

Autoimmune hemolytic anemia associated with Takenouchi-Kosaki syndrome.

Ishikawa K, Uchiyama T, Kaname T, Kawai T, Ishiguro A. Ishikawa K, et al. Among authors: uchiyama t. Pediatr Int. 2021 Dec;63(12):1528-1530. doi: 10.1111/ped.14651. Epub 2021 Aug 17. Pediatr Int. 2021. PMID: 34403170 No abstract available.

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