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[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology|December 27, 2008
[Usefulness of immunofluorescence analysis of neutrophil nonmuscle myosin heavy chain-A for diagnosing in two sisters with May-Hegglin anomaly]Noriko Kimura, Masanori Matsumoto, Katsuya Matsumoto, et al.Journal of Pediatric Hematology/Oncology|December 5, 2017
Macrothrombocytopenia With Congenital Bilateral Cataracts: A Phenotype of MYH9 Disorder With Exon 24 Indel MutationsTakahiro Aoki, Shinji Kunishima, Yoshiharu Yamashita, et al.European Journal of Internal Medicine|May 29, 2025
Natural history of the severe subtype of MYH9-related disease (Epstein syndrome)Kazuma Shinno, Shinji Kunishima, Atsushi Sakamoto, et al.European Journal of Haematology|September 19, 2006
Molecular genetic analysis of a variant Bernard-Soulier syndrome due to compound heterozygosity for two novel glycoprotein Ibbeta mutationsShinji Kunishima, Masahiro Sako, Tomio Yamazaki, et al.American Journal of Hematology|November 26, 2002
Novel nonsense mutation in the platelet glycoprotein Ibbeta gene associated with Bernard-Soulier syndromeShinji Kunishima, Tadashi Matsushita, Takahiko Ito, et al.Journal of Pediatric Hematology/Oncology|September 1, 2004
A Unique Immunofluorescence Method Promotes Accurate Diagnosis in MYH9 Disorders: A Case ReportMiyako Yoshinari, Shinji Kunishima, Shigeaki Miyabayashi, et al.European Journal of Haematology|December 19, 2013
TUBB1 mutation disrupting microtubule assembly impairs proplatelet formation and results in congenital macrothrombocytopeniaShinji Kunishima, Satoshi Nishimura, Hidenori Suzuki, et al.Journal of Human Genetics|September 17, 2010
FLNA p.V528M substitution is neither associated with bilateral periventricular nodular heterotopia nor with macrothrombocytopeniaShinji Kunishima, Yoshimi Ito-Yamamura, Akira Hayakawa, et al.Blood|October 14, 2008
Mutation of the beta1-tubulin gene associated with congenital macrothrombocytopenia affecting microtubule assemblyShinji Kunishima, Ryoji Kobayashi, Tomohiko J Itoh, et al.Thrombosis Research|August 18, 2015
A family having type 2B von Willebrand disease with a novel VWF p.R1308S mutation: Detection of characteristic platelet aggregates on peripheral blood smears as the key aspect of diagnosisKyoko Hatta, Shinji Kunishima, Hiroki Suganuma, et al.Pageof 11