Papers - MATSUSHITA Masaki
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Factors associated with an unfavourable outcome after Salter innominate osteotomy in patients with unilateral developmental dysplasia of the hip: Does occult dysplasia of the contralateral hip affect the outcome? Invited Reviewed
Kaneko H, Kitoh H, Mishima K, Matsushita M, Kadono I, Ishiguro N, Hattori T
Bone Joint J Vol. 96-B ( 10 ) page： 1419 - 1423 2014.10
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Early and late fracture following extensive limb lengthening in achondroplasia and hypochondroplasia Invited Reviewed
Kitoh H, Kaneko H, Mishima K, Matsushita M, Kadono I, Nishida Y, Ishiguro N
Bone Joint J Vol. 96-B ( 9 ) page： 1269 - 1273 2014.9
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Radiographic characteristics of the hand and cervical spine in fibrodysplasia ossificans progressiva Invited Reviewed
Mishima K, Kitoh H, Haga N, Nakashima Y, Kamizono J, Katagiri T, Susami T, Matsushita M, Ishiguro N
Intractable Rare Dis Res Vol. 3 ( 2 ) page： 46 - 51 2014.5
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A case of severe proximal focal femoral deficiency with overlapping phenotypes of Al-Awadi-Raas-Rothschild syndrome and Fuhrmann syndrome Reviewed
Matsushita M, Kitoh H, Mishima K, Nishida Y, Ishiguro N
Ped Radiol Vol. 44 page： 1617-1619 2014
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Benign prenatal hypophosphatasia: a treatable disease not to be missed Reviewed
Matsushita M, Kitoh H, Michigami T, Tachikawa K, Kaneko H, Mishima K, Ishiguro N
Ped Radiol Vol. 44 page： 340-343 2014
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A novel in-flame 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 page： 96-99 2014
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A comparative study of blade plate fixation and external fixation in osteotomies for slipped capital femoral epiphysis Invited Reviewed
Kitoh H, Kitakoji T, Hattori T, Kaneko H, Mishima K, Matsushita M, Ishiguro N
J Pediatr Orthop B Vol. 22 ( 6 ) page： 542 - 547 2013.11
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Perhexiline maleate in the treatment of fibrodysplasia ossificans progressiva: an open-labeled clinical trial Invited Reviewed
Kitoh H, Achiwa M, Kaneko H, Mishima K, Matsushita M, Kadono I, Horowitz JD, Sallustio BC, Ohno K, Ishiguro N
Orphanet J Rare Dis Vol. 8 page： 163 2013.10
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Long-term outcome of gradual reduction using overhead traction for developmental dysplasia of the hip over 6 months of age Invited Reviewed
Kaneko H, Kitoh H, Mishima K, Matsushita M, Ishiguro N
J Pediatr Orthop Vol. 33 ( 6 ) page： 628 - 634 2013.9
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Prognostic factors for trochanteric overgrowth after containment treatment in Legg-Calvé-Perthes disease Invited Reviewed
Kitoh H, Kaneko H, Mishima K, Matsushita M, Ishiguro N
J Pediatr Orthop B Vol. 22 ( 5 ) page： 432 - 436 2013.9
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Clinically applicable antianginal agents suppress osteoblastic transformation of myogenic cells and heterotopic ossifications in mice Invited Reviewed
Yamamoto R, Matsushita M, Kitoh H, Masuda A, Ito M, Katagiri T, Kawai T, Ishiguro N, Ohno K
J Bone Miner Metab Vol. 31 ( 1 ) page： 26 - 33 2013.1
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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 page： 177-182 2013
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Meclozine facilitates chondrocyte proliferation and differentiation by attenuating abnormally activated fibroblast growth factor receptor 3 (FGFR3) signaling in achondroplasia Reviewed
Matsushita M, Kitoh H, Ohkawara B, Mishima K, Kaneko H, Ito M, Masuda A, Ishiguro N, Ohno K
PLoS One Vol. 8 page： e81569 2013
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A novel SOX9 H169Q mutation in a family with overlapping phenotype of mild campomelic dysplasia and small patella syndrome Reviewed
Matsushita M, Kitoh H, Kaneko H, Mishima K, Kadono I, Ishiguro N, Nishmura G
Am J Med Genet A Vol. 161 page： 2528-2534 2013
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Isolated bifid rib: clinical and radiological findings in children Invited Reviewed
Kaneko H, Kitoh H, Mabuchi A, Mishima K, Matsushita M, Ishiguro N
Pediatr Int Vol. 54 ( 6 ) page： 820 - 823 2012.12
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Novel compound heterozygous mutations in the cathepsin K gene in Japanese female siblings with pyknodysostosis Reviewed
Matsushita M, Kitoh H, Kaneko H, Mishima K, Itoh Y, Hattori T, Ishiguro N
Mol Syndromol Vol. 2 page： 254-258 2012