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1

Immature platelet fraction measurement is influenced by platelet size and is a useful parameter for discrimination of macrothrombocytopenia

Miyazaki, Koji, Koike, Yukako, Kunishima, Shinji, Ishii, Ryuji, Danbara, Mikio, Horie, Ryouichi, Yatomi, Yutaka, Higashihara, Masaaki

Journal:

Hematology (Maney Publishing)

Year:

2015

Language:

english

File:

PDF, 418 KB

english, 2015

2

Spectrum of the Mutations in Bernard-Soulier Syndrome

Savoia, Anna, Kunishima, Shinji, De Rocco, Daniela, Zieger, Barbara, Rand, Margaret L., Pujol-Moix, Nuria, Caliskan, Umran, Tokgoz, Huseyin, Pecci, Alessandro, Noris, Patrizia, Srivastava, Alok, Ward,

Journal:

Year:

2014

File:

PDF, 1.86 MB

2014

3

ACTN1rod domain mutation associated with congenital macrothrombocytopenia

Yasutomi, Motoko, Kunishima, Shinji, Okazaki, Shintaro, Tanizawa, Akihiko, Tsuchida, Shinya, Ohshima, Yusei

Journal:

Annals of Hematology

Year:

2016

Language:

english

File:

PDF, 613 KB

english, 2016

4

Perinatal Management for a Pregnant Woman with an MYH9 Disorder

Yamashita, Yuka, Matsuura, Rei, Kunishima, Shinji, Oikawa, Yoshie, Ariizumi, Hirotsugu, Hamada, Shoko, Shirato, Nahoko, Matsuoka, Ryu, Ogawa, Kohichi, Sekizawa, Akihiko

Journal:

Case Reports in Obstetrics and Gynecology

Year:

2016

Language:

english

File:

PDF, 1.47 MB

english, 2016

5

Vulnerable mutation Trp126 → stop of glycoprotein IX in Japanese Bernard – Soulier syndrome

Masako Iwanaga, Shinji Kunishima, Shuichi Ikeda, Masao Tomonaga, Tomoki Naoe

Journal:

European Journal of Haematology

Year:

1998

Language:

english

File:

PDF, 238 KB

english, 1998

6

Somatic mosaicism in MYH9 disorders: the need to carefully evaluate apparently healthy parents

Kunishima, Shinji, Kitamura, Katsumasa, Matsumoto, Tae, Sekine, Takashi, Saito, Hidehiko

Journal:

British Journal of Haematology

Year:

2014

Language:

english

File:

PDF, 184 KB

english, 2014

7

Exon skipping causes atypical phenotypes associated with a loss-of-function mutation in FLNA by restoring its protein function

Oda, Hirotsugu, Sato, Tatsuhiro, Kunishima, Shinji, Nakagawa, Kenji, Izawa, Kazushi, Hiejima, Eitaro, Kawai, Tomoki, Yasumi, Takahiro, Doi, Hiraku, Katamura, Kenji, Numabe, Hironao, Okamoto, Shinya, N

Journal:

European Journal of Human Genetics

Year:

2015

Language:

english

File:

PDF, 633 KB

english, 2015

8

Novel ACTN1 variants in cases of thrombocytopenia

Vincenot, Anne, Saultier, Paul, Kunishima, Shinji, Poggi, Marjorie, Hurtaud-Roux, Marie-Françoise, Roussel, Alain, Schlegel, Nicole, Alessi, Marie-Christine

Journal:

Year:

2019

Language:

english

File:

PDF, 717 KB

english, 2019

9

Diagnosis of inherited platelet disorders on a blood smear: a tool to facilitate worldwide diagnosis of platelet disorders

Greinacher, Andreas, Pecci, Alessandro, Kunishima, Shinji, Althaus, Karina, Nurden, Paquita, Balduini, Carlo L, Bakchoul, Tamam

Journal:

Journal of Thrombosis and Haemostasis

Year:

2017

Language:

english

File:

PDF, 643 KB

english, 2017

10

Homozygous Pro74 → Arg Mutation in the Platelet Glycoprotein Ibβ Gene Associated with Bernard-Soulier Syndrome

Kunishima, Shinji, Tomiyama, Yoshiaki, Honda, Shigenori, Fukunishi, Mariko, Hara, Junichi, Inoue, Chikako, Kamiya, Tadashi, Saito, Hidehiko

Journal:

Thrombosis and Haemostasis

Year:

2000

Language:

english

File:

PDF, 143 KB

english, 2000

11

Renin-angiotensin System Blockade Therapy for Early Renal Involvement in MYH9-related Disease with an E1841K Mutation: A Case Report

Tanaka, Mari, Miki, Sho, Saita, Hirona, Shimada, Hiroki, Nishikawa, Seira, Taniguchi, Keisuke, Hagihara, Koichiro, Iwanari, Sachio, Ikeda, Masaki, Kunishima, Shinji, Takeoka, Hiroya

Journal:

Internal Medicine

Year:

2019

File:

PDF, 1.04 MB

2019

12

Detection of unique neutrophil non-muscle myosin heavy chain-A localization by immunofluorescence analysis in MYH9 disorder presented with macrothrombocytopenia without leukocyte inclusions and deafness

Shinji Kunishima, Tadashi Matsushita, Motoaki Shiratsuchi, Takuya Ikuta, Junji Nishimura, Motohiro Hamaguchi, Tomoki Naoe, Hidehiko Saito

Journal:

European Journal of Haematology

Year:

2005

Language:

english

File:

PDF, 267 KB

english, 2005

13

Transient macrothrombocytopenia associated with maternal-neonatal HPA-21bw incompatibility

Kunishima, Shinji, Hayakawa, Akira, Fujita, Kaori, Saito, Hidehiko

Journal:

Thrombosis Research

Year:

2013

Language:

english

File:

PDF, 245 KB

english, 2013

14

Novel heterozygous missense mutation in the platelet glycoprotein Ibβ gene associated with isolated giant platelet disorder

Shinji Kunishima, Tomoki Naoe, Tadashi Kamiya, Hidehiko Saito

Journal:

American Journal of Hematology

Year:

2001

Language:

english

File:

PDF, 408 KB

english, 2001

15

Macrothrombocytopenia With Congenital Bilateral Cataracts

Aoki, Takahiro, Kunishima, Shinji, Yamashita, Yoshiharu, Minamitani, Kanshi, Ota, Setsuo

Journal:

Journal of Pediatric Hematology/Oncology

Year:

2017

Language:

english

File:

PDF, 144 KB

english, 2017

16

Early diagnosis improves the quality of life in MYH9 disorder

Mitsutaka Shiota, Shinji Kunishima, Takayuki Hamabata, Masatoshi Nakata, Daisuke Hata

Journal:

Pediatric Blood & Cancer

Year:

2012

Language:

english

File:

PDF, 96 KB

english, 2012

17

Demonstration of novel gain-of-function mutations of αIIbβ3: association with macrothrombocytopenia and glanzmann thrombasthenia-like phenotype

Kashiwagi, Hirokazu, Kunishima, Shinji, Kiyomizu, Kazunobu, Amano, Yoshiro, Shimada, Hiroyuki, Morishita, Masashi, Kanakura, Yuzuru, Tomiyama, Yoshiaki

Journal:

Molecular Genetics & Genomic Medicine

Year:

2013

Language:

english

File:

PDF, 2.67 MB

english, 2013

18

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 diagnosis

Hatta, Kyoko, Kunishima, Shinji, Suganuma, Hiroki, Tanaka, Noboru, Ohkawa, Natsuki, Shimizu, Toshiaki

Journal:

Thrombosis Research

Year:

2015

Language:

english

File:

PDF, 782 KB

english, 2015

19

Determination of Glycocalicin in Platelet Concentrate Supernatants Stored in a Synthetic Medium (Seto Solution)

Shinji Kunishima, Tetsuo Shimizu, Shinichi Kora, Tadashi Kamiya, Kazuo Ozawa

Journal:

Year:

1998

File:

PDF, 165 KB

1998

20

A Japanese pedigree with a p.A95V mutation in theMYH9gene demonstrates inherited macrothrombocytopenia without Alport manifestations

Yokoi, Setsuri, Kunishima, Shinji, Takahashi, Yoshiyuki, Morishita, Masashi, Kojima, Seiji

Journal:

Annals of Hematology

Year:

2016

Language:

english

File:

PDF, 328 KB

english, 2016

21

Late onset and high-frequency dominant hearing loss in a family withMYH9disorder

Wasano, Koichiro, Matsunaga, Tatsuo, Ogawa, Kaoru, Kunishima, Shinji

Journal:

European Archives of Oto-Rhino-Laryngology

Year:

2016

Language:

english

File:

PDF, 778 KB

english, 2016

22

Efficacy of neutrophil non-muscle myosin heavy chain-IIA immunofluorescence analysis in determining the pathogenicity ofMYH9variants

Kunishima, Shinji, Yusuke, Okuno, Muramatsu, Hideki, Kojima, Daiei, Nagai, Noriko, Takahashi, Yoshiyuki, Kojima, Seiji

Journal:

Annals of Hematology

Year:

2017

Language:

english

File:

PDF, 356 KB

english, 2017

23

Historical hematology: May–Hegglin anomaly

Hidehiko Saito, Shinji Kunishima

Journal:

American Journal of Hematology

Year:

2008

Language:

english

File:

PDF, 124 KB

english, 2008

24

Application of 16S ribosomal RNA gene amplification to the rapid identification of bacteria from blood culture bottles

Shinji Kunishima, Chikako Inoue, Zenichiro Nishimoto, Tadashi Kamiya, Kazuo Ozawa

Journal:

Transfusion (Wiley)

Year:

2000

Language:

english

File:

PDF, 38 KB

english, 2000

25

Bernard-Soulier Syndrome due to GPIX W127X Mutation in Japan Is Frequently Misdiagnosed as Idiopathic Thrombocytopenic Purpura

Shinji Kunishima, Toshiki Yamada, Motohiro Hamaguchi, Hidehiko Saito

Journal:

International Journal of Hematology

Year:

2006

Language:

english

File:

PDF, 68 KB

english, 2006

26

Poor clinical significance of p53 gene polymorphism in acute myeloid leukemia

Yasuyuki Nakano, Tomoki Naoe, Hitoshi Kiyoi, Shinji Kunishima, Saburo Minami, Shuichi Miyawaki, Norio Asou, Kazutaka Kuriyama, Hidehiko Saito, Ryuzo Ohno

Journal:

Leukemia Research

Year:

2000

Language:

english

File:

PDF, 74 KB

english, 2000

27

A family having type 2B von Willebrand disease with an R1306W mutation: Severe thrombocytopenia leads to the normalization of high molecular weight multimers

Michio Ozeki, Shinji Kunishima, Kimiko Kasahara, Michinori Funato, Takahide Teramoto, Hideo Kaneko, Toshiyuki Fukao, Naomi Kondo

Journal:

Thrombosis Research

Year:

2010

Language:

english

File:

PDF, 693 KB

english, 2010

28

Bernard-Soulier Syndrome due to Compound Heterozygosity for a Novel Glycoprotein Ib� Mutation

Sato, Tetsuji, Kunishima, Shinji, Shirayama, Rie, Ichikawa, Shun, Sakai, Michio, Kusuhara, Koichi

Journal:

Acta Haematologica

Year:

2014

Language:

english

File:

PDF, 129 KB

english, 2014

29

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

Ogawa, Yoshiyuki, Kunishima, Shinji, Yanagisawa, Kunio, Osaki, Yohei, Uchiyama, Yuri, Matsumoto, Naomichi, Tokiniwa, Hideaki, Horiguchi, Jun, Nojima, Yoshihisa, Handa, Hiroshi

Journal:

International Journal of Hematology

Year:

2017

Language:

english

File:

PDF, 855 KB

english, 2017

30

Diagnosis and treatment of MYH9- RD in an Australasian cohort with thrombocytopenia

Rabbolini, David J., Chun, Yenna, Latimer, Maya, Kunishima, Shinji, Fixter, Kathleen, Valecha, Bhavia, Tan, Peter, Chew, Lee Ping, Kile, Benjamin T., Burt, Rachel, Radhakrishnan, Kottayam, Bird, Rober

Journal:

Year:

2017

Language:

english

File:

PDF, 871 KB

english, 2017

31

Microtubule polyglutamylation and acetylation drive microtubule dynamics critical for platelet formation

van Dijk, Juliette, Bompard, Guillaume, Cau, Julien, Kunishima, Shinji, Rabeharivelo, Gabriel, Mateos-Langerak, Julio, Cazevieille, Chantal, Cavelier, Patricia, Boizet-Bonhoure, Brigitte, Delsert, Cla

Journal:

Year:

2018

Language:

english

File:

PDF, 2.78 MB

english, 2018

32

Accumulation of MYH9 mRNA at leukocyte inclusion bodies in MYH9 disorders

Shinji Kunishima, Kyoko Hirano, Motohiro Hamaguchi, Hidehiko Saito

Journal:

European Journal of Haematology

Year:

2008

Language:

english

File:

PDF, 107 KB

english, 2008

33

Familial cases with MYH9 disorders caused by MYH9 S96L mutation

Murayama, Shizuko, Akiyama, Masaharu, Namba, Hiroyuki, Wada, Yasuyuki, Ida, Hiroyuki, Kunishima, Shinji

Journal:

Pediatrics International

Year:

2013

Language:

english

File:

PDF, 425 KB

english, 2013

34

Gata-1 transcription factor is mutated in cmk megakaryoblastic cell line

Shinji Kunishima, Tetsuhito Kojima, Chikako Inoue, Tadashi Kamiya, Hidehiko Saito

Journal:

British Journal of Haematology

Year:

2003

Language:

english

File:

PDF, 78 KB

english, 2003

35

Immunofluorescence Analysis of Neutrophil Nonmuscle Myosin Heavy Chain-A in MYH9 Disorders: Association of Subcellular Localization with MYH9 Mutations

Kunishima, Shinji, Matsushita, Tadashi, Kojima, Tetsuhito, Sako, Masahiro, Kimura, Fumihiro, Jo, Eun-Kyeong, Inoue, Chikako, Kamiya, Tadashi, Saito, Hidehiko

Journal:

Laboratory Investigation

Year:

2003

Language:

english

File:

PDF, 1.58 MB

english, 2003

36

Molecular genetic analysis of a variant Bernard–Soulier syndrome due to compound heterozygosity for two novel glycoprotein Ibβ mutations

Shinji Kunishima, Masahiro Sako, Tomio Yamazaki, Motohiro Hamaguchi, Hidehiko Saito

Journal:

European Journal of Haematology

Year:

2006

Language:

english

File:

PDF, 506 KB

english, 2006

37

Successful immunostaining demonstrates abnormal intracytoplasmic MYH9 protein (NMMHC-IIA) in neutrophils of a dog with May-Hegglin anomaly

Bente Flatland, Shinji Kunishima

Journal:

Veterinary Clinical Pathology

Year:

2011

Language:

english

File:

PDF, 81 KB

english, 2011

38

Bernard-Soulier syndrome caused by a hemizygous GPIbβ mutation and 22q11.2 deletion

Kunishima, Shinji, Imai, Tsuyoshi, Kobayashi, Ryoji, Kato, Motohiro, Ogawa, Seishi, Saito, Hidehiko

Journal:

Pediatrics International

Year:

2013

Language:

english

File:

PDF, 361 KB

english, 2013

39

The synergistic effect of BCR signaling inhibitors combined with an HDAC inhibitor on cell death in a mantle cell lymphoma cell line

Hagiwara, Kazumi, Kunishima, Shinji, Iida, Hiroatsu, Miyata, Yasuhiko, Naoe, Tomoki, Nagai, Hirokazu

Journal:

Year:

2015

Language:

english

File:

PDF, 1.01 MB

english, 2015

40

A novelMYH9mutation in a patient withMYH9disorders and platelet size-specific effect of romiplostim on macrothrombocytopenia

Yamanouchi, Jun, Hato, Takaaki, Kunishima, Shinji, Niiya, Toshiyuki, Nakamura, Hisashi, Yasukawa, Masaki

Journal:

Annals of Hematology

Year:

2015

Language:

english

File:

PDF, 328 KB

english, 2015

41

New enzyme-linked immunosorbent assay for glycocalicin in plasma

Kunishima, ShinjI, Hayashi, Klyotaka, Kobayashi, Sentaro, Naoe, Tomokl, Ohno, Ryuzo

Journal:

Clinical Chemistry

Year:

1991

File:

PDF, 926 KB

1991

42

Thanks to Reviewers

Kunishima, Shinji, Matsushita, Tadashi, Kojima, Tetsuhito, Sako, Masahiro, Kimura, Fumihiro, Jo, Eun-Kyeong, Inoue, Chikako, Kamiya, Tadashi, Saito, Hidehiko

Journal:

Laboratory Investigation

Year:

2003

Language:

english

File:

PDF, 41 KB

english, 2003

43

Identification and characterization of the first large deletion of the MYH9 gene associated with MYH9 disorders

Shinji Kunishima, Tadashi Matsushita, Motohiro Hamaguchi, Hidehiko Saito

Journal:

European Journal of Haematology

Year:

2008

Language:

english

File:

PDF, 235 KB

english, 2008

44

Corrigendum to “A family having type 2B von Willebrand disease with an R1306W mutation: Severe thrombocytopenia leads to the normalization of high molecular weight multimers” [Thrombosis Research 125 (2010) e17–e22]

Michio Ozeki, Shinji Kunishima, Kimiko Kasahara, Michinori Funato, Takahide Teramoto, Hideo Kaneko, Toshiyuki Fukao, Naomi Kondo

Journal:

Thrombosis Research

Year:

2010

Language:

english

File:

PDF, 120 KB

english, 2010

45

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

Suzuki, Nobuaki, Kunishima, Shinji, Ikejiri, Makoto, Maruyama, Shoichi, Sone, Michihiko, Takagi, Akira, Ikawa, Masahito, Okabe, Masaru, Kojima, Tetsuhito, Saito, Hidehiko, Naoe, Tomoki, Matsushita, Ta

Journal:

Year:

2013

Language:

english

File:

PDF, 11.86 MB

english, 2013

46

First description of somatic mosaicism in MYH9 disorders

Shinji Kunishima, Tadashi Matsushita, Takao Yoshihara, Yoko Nakase, Kentaro Yokoi, Motohiro Hamaguchi, Hidehiko Saito

Journal:

British Journal of Haematology

Year:

2005

Language:

english

File:

PDF, 165 KB

english, 2005

47

Efficacy of inchinkoto for a patient with liver fibrosis complicated with transient abnormal myelopoiesis in Down's syndrome

Masahiro Takeyama, Yumiko Uchida, Ikuyo Arai, Tomoyuki Kamamoto, Toshiya Nishikubo, Hiromichi Kanehiro, Toshiyuki Sado, Shinji Kunishima, Yukihiro Takahashi

Journal:

Pediatrics International

Year:

2011

Language:

english

File:

PDF, 2.22 MB

english, 2011

48

Increased but highly dispersed levels of plasma glycocalicin in patients with disseminated intravascular coagulation

Shinji Kunishima, Sentaro Kobayashi, Tomoki Naoe

Journal:

European Journal of Haematology

Year:

1996

Language:

english

File:

PDF, 488 KB

english, 1996

49

Xq26.1-26.2 gain identified on array comparative genomic hybridization in bilateral periventricular nodular heterotopia with overlying polymicrogyria

Abe, Yu, Kikuchi, Atsuo, Kobayashi, Satoru, Wakusawa, Keisuke, Tanaka, Soichiro, Inui, Takehiko, Kunishima, Shinji, Kure, Shigeo, Haginoya, Kazuhiro

Journal:

Developmental Medicine & Child Neurology

Year:

2014

Language:

english

File:

PDF, 383 KB

english, 2014

50

First Turkish Case of Bernard-Soulier Syndrome Associated with GPIX N45S

Da&gbreve, &inodot, stan, Necati, Kunishima, Shinji

Journal:

Acta Haematologica

Year:

2007

Language:

english

File:

PDF, 97 KB

english, 2007

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