Papers - MATSUSHITA Masaki
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Long term health-related quality of life in patients with achondroplasia and hypochondroplasia
Matsushita, M; Kitoh, H; Mishima, K; Ishiguro, N; Fujiwara, S; Haga, N; Kitaoka, T; Kubota, T; Ozono, K
JOURNAL OF BONE AND MINERAL RESEARCH Vol. 33 page: 300 - 301 2018.11
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Chronic lateral epiphyseal separation of the proximal tibia causes late-onset tibia vara.
Hasegawa S, Kitoh H, Matsushita M, Mishima K, Kadono I, Sugiura H, Kitamura A, Ishiguro N
Journal of pediatric orthopedics. Part B Vol. 27 ( 1 ) page: 31 - 34 2018.1
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Okura T, Matsushita M, Mishima K, Esaki R, Seki T, Ishiguro N, Kitoh H
Journal of orthopaedic research : official publication of the Orthopaedic Research Society Vol. 36 ( 1 ) page: 300 - 308 2018.1
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A Novel Heterozygous Mutation in the T-box Protein 4 Gene in an Adult Case of Small Patella Syndrome.
Oda T, Matsushita M, Ono Y, Kitoh H, Sakai T
Journal of orthopaedic case reports Vol. 8 ( 1 ) page: 85 - 88 2018.1
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Extensive Bone Lengthening for a Patient with Linear Morphea.
Mishima K, Kitoh H, Matsushita M, Nagata T, Kamiya Y, Ishiguro N
Case reports in orthopedics Vol. 2018 page: 4535804 2018
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Osawa Yusuke, Matsushita Masaki, Hasegawa Sachi, Esaki Ryusaku, Fujio Masahito, Ohkawara Bisei, Ishiguro Naoki, Ohno Kinji, Kitoh Hiroshi
BONE Vol. 105 page: 42 - 49 2017.12
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Okura, T; Matsushita, M; Mishima, K; Seki, T; Ishiguro, N; Kitoh, H
JOURNAL OF BONE AND MINERAL RESEARCH Vol. 32 page: S201 - S201 2017.12
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Matsushita Masaki, Esaki Ryusaku, Mishima Kenichi, Ishiguro Naoki, Ohno Kinji, Kitoh Hiroshi
SCIENTIFIC REPORTS Vol. 7 ( 1 ) page: 7371 2017.8
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Matsushita Masaki, Mishima Kenichi, Iwata Kohji, Hattori Tadashi, Ishiguro Naoki, Kitoh Hiroshi
MEDICINE Vol. 96 ( 19 ) page: e6662 2017.5
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Kohno Yusuke, Nakashima Yasuharu, Kitano Toshio, Irie Taichi, Kita Atsushi, Nakamura Tomoyuki, Endo Hirosuke, Fujii Yosuke, Kuroda Takayuki, Mitani Shigeru, Kitoh Hiroshi, Matsushita Masaki, Hattori Tadashi, Iwata Koji, Iwamoto Yukihide
JOURNAL OF ORTHOPAEDIC SCIENCE Vol. 22 ( 1 ) page: 112 - 115 2017.1
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Matsushita Masaki, Mishima Kenichi, Esaki Ryusaku, Ishiguro Naoki, Ohno Kinji, Kitoh Hiroshi
JOURNAL OF NEUROSURGERY-PEDIATRICS Vol. 19 ( 1 ) page: 91 - 95 2017.1
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Maternal administration of meclozine for the treatment of foramen magnum stenosis in transgenic mice with achondroplasia
Matsushita M, Mishima K, Esaki R, Ishiguro N, Ohno K, Kitoh H
J Neurosurg Pediatr Vol. 19 page: 91-95 2017
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[Risk factors for rebleeding and risk-based follow-up of obscure gastrointestinal bleeding after its initial diagnosis].
Uchida G, Nakamura M, Watanabe O, Yamamura T, Matsushita M, Ishikawa T, Furukawa K, Funasaka K, Ohno E, Kawashima H, Miyahara R, Goto H, Hirooka Y
Nihon Shokakibyo Gakkai zasshi = The Japanese journal of gastro-enterology Vol. 114 ( 10 ) page: 1819 - 1829 2017
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Clinical Results and Complications of Lower Limb Lengthening for Fibular Hemimelia: A Report of Eight Cases. Invited Reviewed
Mishima K, Kitoh H, Iwata K, Matsushita M, Nishida Y, Hattori T, Ishiguro N
Medicine (Baltimore) Vol. 95 ( 21 ) page: e3787 2016.5
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Tranilast stimulates endochondral ossification by upregulating SOX9 and RUNX2 promoters Invited Reviewed
Hasegawa S, Kitoh H, Ohkawara B, Mishima K, Matsushita M, Masuda A, Ishiguro N, Ohno K
Biochem Biophys Res Commun Vol. 470 ( 2 ) page: 356 - 361 2016.2
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Characterisation of novel RUNX2 mutation with alanine tract expansion from Japanese cleidocranial dysplasia patient Invited Reviewed
Shibata A, Machida J, Yamaguchi S, Kimura M, Tatematsu T, Miyachi H, Matsushita M, Kitoh H, Ishiguro N, Nakayama A, Higashi Y, Shimozato K, Tokita Y
Mutagenesis Vol. 31 ( 1 ) page: 61 - 67 2016.1
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Low bone mineral density in achondroplasia and hypochondroplasia Reviewed
Matsushita M, Kitoh H, Mishima K, Kadono I, Sugiura H, Hasegawa S, Nishida Y, Ishiguro N
Pediatr Int page: 10.1111/ped.12890 2016
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Prediction of Clinically Significant Leg-Length Discrepancy in Congenital Disorders Invited Reviewed
Mishima K, Kitoh H, Kadono I, Matsushita M, Sugiura H, Hasegawa S, Kitamura A, Nishida Y, Ishiguro N
Orthopedics Vol. 38 ( 10 ) page: e919 - e924 2015.10
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Meclozine promotes lomgitudinal skeletal growth in transgenic mice with achondroplasia carrying a gain-of-function mutation in the FGFR3 gene Reviewed
Matsushita M, Hasegawa S, Kitoh H, Mori K, Ohkawara B, Yasoda A, Masuda A, Ishiguro N, Ohno K
Endocrinology Vol. 156 page: 548-554 2015
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A glutamine repeat variant of the RUNX2 gene causes cleidocranial dysplasia Reviewed
Matsushita M, Kitoh H, Subasioglu A, Colak FK, Dundar M, Mishima K, Nishida Y, Ishiguro N
Mol Syndromol page: in press 2015