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International Journal of Laboratory Hematology|June 17, 2023
Measurement of immature platelet fraction is useful in the differential diagnosis of MYH9 disordersHiroyoshi Kouno, Shinji Kunishima, Junko Takebe, et al.
British Journal of Haematology|January 26, 2005
First description of somatic mosaicism in MYH9 disordersShinji Kunishima, Tadashi Matsushita, Takao Yoshihara, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|May 19, 2009
A novel homozygous 8-base pair deletion mutation in the glycoprotein Ibalpha gene in a patient with Bernard-Soulier syndromeChihaya Imai, Shinji Kunishima, Takayuki Takachi, et al.
International Journal of Hematology|March 26, 2021
ETV6-related thrombocytopenia associated with a transient decrease in von Willebrand factorYuri Kanamaru, Toru Uchiyama, Tadashi Kaname, et al.
International Journal of Hematology|April 16, 2024
Bernard-Soulier syndrome caused by a novel GP1BB variant and 22q11.2 deletionRintaro Nagoshi, Atsushi Sakamoto, Tsuyoshi Imai, et al.
Hemasphere|November 15, 2019
Anagrelide Modulates Proplatelet Formation Resulting in Decreased Number and Increased Size of PlateletsNaohiro Miyashita, Masahiro Onozawa, Shota Yokoyama, et al.
American Journal of Medical Genetics. Part A|February 14, 2022
Platelet function and filamin A expression in two families with novel FLNA gene mutations associated with periventricular nodular heterotopia and panlobular emphysemaLaura M Tanner, Shinji Kunishima, Elina Lehtinen, et al.
European Journal of Haematology|January 16, 2008
Characterization of a patient with atypical amegakaryocytic thrombocytopeniaSachiko Kanaji, Taisuke Kanaji, Masahiro Migita, et al.
Hematology (Amsterdam, Netherlands)|June 3, 2015
Immature platelet fraction measurement is influenced by platelet size and is a useful parameter for discrimination of macrothrombocytopeniaKoji Miyazaki, Yukako Koike, Shinji Kunishima, et al.
European Journal of Haematology|January 24, 2007
Haematological characteristics of MYH9 disorders due to MYH9 R702 mutationsShinji Kunishima, Miyako Yoshinari, Hisanori Nishio, et al.
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