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ArticlesPeer ReviewedFull Text
A nationwide survey of MYH9-related disease in Japan
Author / Creator:Shirai, Yoko ; Miura, Kenichiro ; Hamada, Riku ; Ishikura, Kenji ; Kunishima, Shinji ; Hattori, Motoshi
Publisher:Tokyo: Springer Nature B.V
Journal title:Clinical and experimental nephrology, 2024-01, Vol.28 (1), p.40-49
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ETV6-related thrombocytopenia associated with a transient decrease in von Willebrand factor
Author / Creator:Kanamaru Yuri ; Uchiyama Toru ; Kaname Tadashi ; Yanagi Kumiko ; Ohara Osamu ; Kunishima Shinji ; Ishiguro Akira
Publisher:Tokyo: Springer Nature B.V
Journal title:International journal of hematology, 2021-08, Vol.114 (2), p.297-300
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Thrombosis from a Prothrombin Mutation Conveying Antithrombin Resistance
Author / Creator:Miyawaki, Yuhri ; Suzuki, Atsuo ; Fujita, Junko ; Maki, Asuka ; Okuyama, Eriko ; Murata, Moe ; Takagi, Akira ; Murate, Takashi ; Kunishima, Shinji ; Sakai, Michio ; Okamoto, Kohji ; Matsushita, Tadashi ; Naoe, Tomoki ; Saito, Hidehiko ; Kojima, Tetsuhito
Publisher:Waltham, MA: Massachusetts Medical Society
Journal title:The New England journal of medicine, 2012-06, Vol.366 (25), p.2390-2396
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Inherited macrothrombocytopenia due to a novel splice donor site mutation in ITGB3
Author / Creator:Komeno, Yukiko ; Uchiyama, Toru ; Kawano, Fuyuko ; Kurihara, Yuya ; Kurokawa, Mineo ; Ohara, Osamu ; Kunishima, Shinji ; Ishiguro, Akira
Publisher:Berlin: Springer Nature B.V
Journal title:Annals of hematology, 2023-10, Vol.102 (10), p.2947-2949
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Splenectomy as an effective treatment for macrothrombocytopenia in Takenouchi-Kosaki syndrome
Author / Creator:Yamano, Shio ; Iguchi, Akihiro ; Ishikawa, Kotaro ; Sakamoto, Atsushi ; Uchiyama, Toru ; Yanagi, Kumiko ; Kaname, Tadashi ; Kunishima, Shinji ; Ishiguro, Akira
Publisher:Tokyo: Springer Nature B.V
Journal title:International journal of hematology, 2023-04, Vol.117 (4), p.622-625
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Clinical utility of next-generation sequencing for inherited bone marrow failure syndromes
Author / Creator:Muramatsu, Hideki ; Okuno, Yusuke ; Yoshida, Kenichi ; Shiraishi, Yuichi ; Doisaki, Sayoko ; Narita, Atsushi ; Sakaguchi, Hirotoshi ; Kawashima, Nozomu ; Wang, Xinan ; Xu, Yinyan ; Chiba, Kenichi ; Tanaka, Hiroko ; Hama, Asahito ; Sanada, Masashi ; Takahashi, Yoshiyuki ; Kanno, Hitoshi ; Yamaguchi, Hiroki ; Ohga, Shouichi ; Manabe, Atsushi ; Harigae, Hideo ; Kunishima, Shinji ; Ishii, Eiichi ; Kobayashi, Masao ; Koike, Kenichi ; Watanabe, Kenichiro ; Ito, Etsuro ; Takata, Minoru ; Yabe, Miharu ; Ogawa, Seishi ; Miyano, Satoru ; Kojima, Seiji
Publisher:New York: Nature Publishing Group US
Journal title:Genetics in medicine, 2017-07, Vol.19 (7), p.796-802
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ArticlesPeer ReviewedFull Text
Microtubule polyglutamylation and acetylation drive microtubule dynamics critical for platelet formation
Author / Creator:van Dijk, Juliette ; Bompard, Guillaume ; Cau, Julien ; Kunishima, Shinji ; Rabeharivelo, Gabriel ; Mateos-Langerak, Julio ; Cazevieille, Chantal ; Cavelier, Patricia ; Boizet-Bonhoure, Brigitte ; Delsert, Claude ; Morin, Nathalie
Publisher:England: BioMed Central Ltd
Journal title:BMC biology, 2018-10, Vol.16 (1), p.116-17, Article 116
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Anesthetic management without perioperative platelet transfusion for cervical laminectomy and laminoplasty in a case of May–Hegglin anomaly
Author / Creator:Kumemura, Masateru ; Omae, Takeshi ; Kou, Keito ; Sakuraba, Sonoko ; Niimi, Naoko ; Kunishima, Shinji
Publisher:Tokyo: Springer Japan
Journal title:Journal of anesthesia, 2018-08, Vol.32 (4), p.641-644
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Establishment of Mouse Model of MYH9 Disorders: Heterozygous R702C Mutation Provokes Macrothrombocytopenia with Leukocyte Inclusion Bodies, Renal Glomerulosclerosis and Hearing Disability
Author / Creator:Suzuki, Nobuaki ; Kunishima, Shinji ; Ikejiri, Makoto ; Maruyama, Shoichi ; Sone, Michihiko ; Takagi, Akira ; Ikawa, Masahito ; Okabe, Masaru ; Kojima, Tetsuhito ; Saito, Hidehiko ; Naoe, Tomoki ; Matsushita, Tadashi
Publisher:United States: Public Library of Science
Journal title:PloS one, 2013-08, Vol.8 (8), p.e71187
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Efficacy of neutrophil non-muscle myosin heavy chain-IIA immunofluorescence analysis in determining the pathogenicity of MYH9 variants
Author / Creator:Kunishima, Shinji ; Yusuke, Okuno ; Muramatsu, Hideki ; Kojima, Daiei ; Nagai, Noriko ; Takahashi, Yoshiyuki ; Kojima, Seiji
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Annals of hematology, 2017-06, Vol.96 (6), p.1065-1066
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11q23 deletion syndrome (Jacobsen syndrome) with severe bleeding: a case report
Author / Creator:Ichimiya, Yuko ; Wada, Yuka ; Kunishima, Shinji ; Tsukamoto, Keiko ; Kosaki, Rika ; Sago, Haruhiko ; Ishiguro, Akira ; Ito, Yushi
Publisher:England: BioMed Central Ltd
Journal title:Journal of medical case reports, 2018-01, Vol.12 (1), p.3-4, Article 3
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Successful management of perioperative hemostasis in a patient with Glanzmann thrombasthenia who underwent a right total mastectomy
Author / Creator:Ogawa, Yoshiyuki ; Kunishima, Shinji ; Yanagisawa, Kunio ; Osaki, Yohei ; Uchiyama, Yuri ; Matsumoto, Naomichi ; Tokiniwa, Hideaki ; Horiguchi, Jun ; Nojima, Yoshihisa ; Handa, Hiroshi
Publisher:Tokyo: Springer Japan
Journal title:International journal of hematology, 2017-02, Vol.105 (2), p.221-225
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The first two cases of MYH9 disorders in Thailand: an international collaborative study
Author / Creator:Sirachainan, Nongnuch ; Komwilaisak, Patcharee ; Kitamura, Katsumasa ; Hongeng, Suradej ; Sekine, Takashi ; Kunishima, Shinji
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Annals of hematology, 2015-04, Vol.94 (4), p.707-709
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A case of MYH9 disorders caused by a novel mutation (p.K74E)
Author / Creator:Kanematsu, Takeshi ; Suzuki, Nobuaki ; Yoshida, Tadao ; Kishimoto, Mayuko ; Aoki, Tomohiro ; Ogawa, Mika ; Kagami, Yoshitoyo ; Kiyoi, Hitoshi ; Matsushita, Tadashi ; Kunishima, Shinji
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Annals of hematology, 2016-01, Vol.95 (1), p.161-163
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A Brazilian case of Bernard–Soulier syndrome with two distinct founder mutations
Author / Creator:Kanda, Kenji ; Kunishima, Shinji ; Sato, Aya ; Abe, Daisuke ; Nishijima, Setsuko ; Ishigami, Tsuyoshi
Publisher:London: Nature Publishing Group UK
Journal title:Human genome variation, 2017-07, Vol.4 (1), p.17030, Article 17030
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FLNA p.V528M substitution is neither associated with bilateral periventricular nodular heterotopia nor with macrothrombocytopenia
Author / Creator:Kunishima, Shinji ; Ito-Yamamura, Yoshimi ; Hayakawa, Akira ; Yamamoto, Toshimichi ; Saito, Hidehiko
Publisher:London: Nature Publishing Group UK
Journal title:Journal of human genetics, 2010-12, Vol.55 (12), p.844-846
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Two Cases of the MYH9 Disorder Fechtner Syndrome Diagnosed from Observation of Peripheral Blood Cells before End-Stage Renal Failure
Author / Creator:Kunishima, Shinji ; Sakaguchi, Katsuhiko ; Morishima, Atsuyuki ; Okute, Yujiro ; Minami, Tomohiro ; Miki, Sho ; Terashima, Ken ; Kasahara, Hidenori ; Muratsu, Jun ; Teshirogi, Shin ; Yoneda, Suguru
Publisher:Cairo, Egypt: Hindawi Publishing Corporation
Journal title:Case Reports in Nephrology, 2019, Vol.2019 (2019), p.1-6
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Genetic Abnormalities of Bernard-Soulier Syndrome
Author / Creator:Kunishima, Shinji ; Kamiya, Tadashi ; Saito, Hidehiko
Publisher:Tokyo: Springer
Journal title:International journal of hematology, 2002-11, Vol.76 (4), p.319-327
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Transient hemiparesis in a 14-year-old boy with MYH9 disorders
Author / Creator:Kitamura, Katsumasa ; Kunishima, Shinji ; Tahara, Mayu ; Ogiwara, Shigetoshi ; Dobata, Nana ; Dobata, Tomoyuki ; Sugihara, Akemi ; Nakashima, Taiji ; Sasaki, Yasushi ; Nagumo, Kiyoshi ; Kubota, Mitsuru ; Kinugawa, Yoshikazu ; Ieko, Masahiro ; Kumaki, Satoru
Publisher:Japan: Springer Japan
Journal title:International journal of hematology, 2012-09, Vol.96 (3), p.376-379
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Perinatal Management for a Pregnant Woman with an MYH9 Disorder
Author / Creator:Sekizawa, Akihiko ; Ogawa, Kohichi ; Shirato, Nahoko ; Hamada, Shoko ; Ariizumi, Hirotsugu ; Oikawa, Yoshie ; Kunishima, Shinji ; Matsuura, Rei ; Yamashita, Yuka ; Matsuoka, Ryu
Publisher:Cairo, Egypt: Hindawi Publishing Corporation
Journal title:Case reports in obstetrics and gynecology, 2016-01, Vol.2016 (2016), p.1-3
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Showing 1 to 20 of 44 results

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A nationwide survey of MYH9-related disease in Japan

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

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Thrombosis from a Prothrombin Mutation Conveying Antithrombin Resistance

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

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

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Clinical utility of next-generation sequencing for inherited bone marrow failure syndromes

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Microtubule polyglutamylation and acetylation drive microtubule dynamics critical for platelet formation

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Anesthetic management without perioperative platelet transfusion for cervical laminectomy and laminoplasty in a case of May–Hegglin anomaly

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Establishment of Mouse Model of MYH9 Disorders: Heterozygous R702C Mutation Provokes Macrothrombocytopenia with Leukocyte Inclusion Bodies, Renal Glomerulosclerosis and Hearing Disability

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Efficacy of neutrophil non-muscle myosin heavy chain-IIA immunofluorescence analysis in determining the pathogenicity of MYH9 variants

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11q23 deletion syndrome (Jacobsen syndrome) with severe bleeding: a case report

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Successful management of perioperative hemostasis in a patient with Glanzmann thrombasthenia who underwent a right total mastectomy

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The first two cases of MYH9 disorders in Thailand: an international collaborative study

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A case of MYH9 disorders caused by a novel mutation (p.K74E)

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A Brazilian case of Bernard–Soulier syndrome with two distinct founder mutations

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FLNA p.V528M substitution is neither associated with bilateral periventricular nodular heterotopia nor with macrothrombocytopenia

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Two Cases of the MYH9 Disorder Fechtner Syndrome Diagnosed from Observation of Peripheral Blood Cells before End-Stage Renal Failure

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Genetic Abnormalities of Bernard-Soulier Syndrome

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Transient hemiparesis in a 14-year-old boy with MYH9 disorders

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Perinatal Management for a Pregnant Woman with an MYH9 Disorder

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