Papers - MISHIMA Kenichi
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A novel in-frame deletion of the RUNX2 gene causes a classic form of cleidocranial dysplasia Reviewed
Matsushita M, Kitoh H, Kaneko H, Mishima K, Itoh Y, Tokita Y, Ishiguro N.
J Bone Miner Metab. Vol. 32 ( 1 ) page: 96 - 99 2013.4
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Orthopaedic manifestations and diagnostic clues in children with Guillain-Barré syndrome Reviewed
Matsushita M, Kitoh H, Itomi K, Kitakoji T, Iwata K, Mishima K, Ishiguro N, Hattori T.
J Child Orthop. Vol. 7 ( 3 ) page: 177 - 182 2013.1
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骨形成促進効果を有する既存薬の同定とその臨床応用の可能性 Invited Reviewed
三島 健一、鬼頭 浩史、金子 浩史、松下 雅樹、石黒 直樹
日本小児整形外科学会雑誌 2013
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Isolated bifid rib: clinical and radiological findings in children. Reviewed
Kaneko H, Kitoh H, Mabuchi A, Mishima K, Matsushita M, Ishiguro N.
Pediatr Int. Vol. 54 ( 6 ) page: 820 - 823 2012.9
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Early clinical and radiographic characteristics in fibrodysplasia ossificans progressiva: a report of two cases. Reviewed
Mishima K, Kitoh H, Katagiri T, Kaneko H, Ishiguro N.
J Bone Joint Surg Am. page: e52 2011.5