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International Journal of Hematology|December 5, 2002
Genetic abnormalities of Bernard-Soulier syndromeShinji Kunishima, Tadashi Kamiya, Hidehiko SaitoBlood|January 15, 2008
Differential expression of wild-type and mutant NMMHC-IIA polypeptides in blood cells suggests cell-specific regulation mechanisms in MYH9 disordersShinji Kunishima, Motohiro Hamaguchi, Hidehiko SaitoEuropean Journal of Haematology|May 23, 2009
Identification of three in-frame deletion mutations in MYH9 disorders suggesting an important hot spot for small rearrangements in MYH9 exon 24Koji Miyazaki, Shinji Kunishima, Wataru Fujii, et al.Genetic Testing and Molecular Biomarkers|August 4, 2009
Mutations in MYH9 exons 1, 16, 26, and 30 are infrequently found in Japanese patients with nonsyndromic deafnessShinji Kunishima, Tatsuo Matsunaga, Yoshimi Ito, et al.European Journal of Haematology|February 21, 2008
Identification and characterization of the first large deletion of the MYH9 gene associated with MYH9 disordersShinji Kunishima, Tadashi Matsushita, Motohiro Hamaguchi, et al.European Journal of Haematology|March 8, 2006
Novel heterozygous missense mutation in the second leucine rich repeat of GPIbalpha affects GPIb/IX/V expression and results in macrothrombocytopenia in a patient initially misdiagnosed with idiopathic thrombocytopenic purpuraShinji Kunishima, Toshi Imai, Motohiro Hamaguchi, et al.[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology|September 4, 2024
[Developments of high-throughput sequencing-based diagnosis of congenital thrombocytopenia/platelet disorders in a registry study]Akira Ishiguro, Toru Uchiyama, Atsushi Sakamoto, et al.European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|March 5, 2016
Late onset and high-frequency dominant hearing loss in a family with MYH9 disorderKoichiro Wasano, Tatsuo Matsunaga, Kaoru Ogawa, et al.Clinical Nephrology|May 1, 2012
Association of a novel in-frame deletion mutation of the MYH9 gene with end-stage renal failure: case report and review of the literatureMami Ishida, Yasukiyo Mori, Noriyoshi Ota, et al.Journal of Pediatric Hematology/Oncology|September 3, 2004
A unique immunofluorescence method promotes accurate diagnosis in MYH9 disorders: a case reportMiyako Yoshinari, Shinji Kunishima, Shigeaki Miyabayashi, et al.Pageof 11