Kaneko H - Search Results

1

Hyperuricemia cosegregating with osteogenesis imperfecta is associated with a mutation in GPATCH8.

Kaneko H, Kitoh H, Matsuura T, Masuda A, Ito M, Mottes M, Rauch F, Ishiguro N, Ohno K. Kaneko H, et al. Hum Genet. 2011 Nov;130(5):671-83. doi: 10.1007/s00439-011-1006-9. Epub 2011 May 19. Hum Genet. 2011. PMID: 21594610

2

Differential effects of culture-expanded bone marrow cells on the regeneration of bone between the femoral and the tibial lengthenings.

Kitoh H, Kawasumi M, Kaneko H, Ishiguro N. Kitoh H, et al. Among authors: kaneko h. J Pediatr Orthop. 2009 Sep;29(6):643-9. doi: 10.1097/BPO.0b013e3181b2afb2. J Pediatr Orthop. 2009. PMID: 19700998

3

Radiographic analysis of movements of the acetabulum and the femoral head after Salter innominate osteotomy.

Kitoh H, Kaneko H, Ishiguro N. Kitoh H, et al. Among authors: kaneko h. J Pediatr Orthop. 2009 Dec;29(8):879-84. doi: 10.1097/BPO.0b013e3181c1e314. J Pediatr Orthop. 2009. PMID: 19934703

4

Spondylometaphyseal dysplasia with cone-rod dystrophy.

Kitoh H, Kaneko H, Kondo M, Yamamoto T, Ishiguro N, Nishimura G. Kitoh H, et al. Among authors: kaneko h. Am J Med Genet A. 2011 Apr;155A(4):845-9. doi: 10.1002/ajmg.a.33898. Epub 2011 Mar 15. Am J Med Genet A. 2011. PMID: 21412974

5

Early clinical and radiographic characteristics in fibrodysplasia ossificans progressiva: a report of two cases.

Mishima K, Kitoh H, Katagiri T, Kaneko H, Ishiguro N. Mishima K, et al. Among authors: kaneko h. J Bone Joint Surg Am. 2011 May 18;93(10):e52. doi: 10.2106/JBJS.J.01443. J Bone Joint Surg Am. 2011. PMID: 21593359 No abstract available.

6

Chondroblastoma of the femoral neck as a cause of hip synovitis.

Kaneko H, Kitoh H, Wasa J, Nishida Y, Ishiguro N. Kaneko H, et al. J Pediatr Orthop B. 2012 Mar;21(2):179-82. doi: 10.1097/BPB.0b013e3283484c31. J Pediatr Orthop B. 2012. PMID: 21685802

7

Isolated bifid rib: clinical and radiological findings in children.

Kaneko H, Kitoh H, Mabuchi A, Mishima K, Matsushita M, Ishiguro N. Kaneko H, et al. Pediatr Int. 2012 Dec;54(6):820-3. doi: 10.1111/j.1442-200X.2012.03672.x. Epub 2012 Sep 11. Pediatr Int. 2012. PMID: 22640412

8

Novel Compound Heterozygous Mutations in the Cathepsin K Gene in Japanese Female Siblings with Pyknodysostosis.

Matsushita M, Kitoh H, Kaneko H, Mishima K, Itoh Y, Hattori T, Ishiguro N. Matsushita M, et al. Among authors: kaneko h. Mol Syndromol. 2012 Apr;2(6):254-258. doi: 10.1159/000336581. Epub 2012 Mar 6. Mol Syndromol. 2012. PMID: 22822386 Free PMC article.

9

Prognostic factors for trochanteric overgrowth after containment treatment in Legg-Calvé-Perthes disease.

Kitoh H, Kaneko H, Mishima K, Matsushita M, Ishiguro N. Kitoh H, et al. Among authors: kaneko h. J Pediatr Orthop B. 2013 Sep;22(5):432-6. doi: 10.1097/BPB.0b013e32835f585b. J Pediatr Orthop B. 2013. PMID: 23426028

10

A novel in-frame deletion of the RUNX2 gene causes a classic form of cleidocranial dysplasia.

Matsushita M, Kitoh H, Kaneko H, Mishima K, Itoh Y, Tokita Y, Ishiguro N. Matsushita M, et al. Among authors: kaneko h. J Bone Miner Metab. 2014 Jan;32(1):96-9. doi: 10.1007/s00774-013-0456-7. Epub 2013 Apr 5. J Bone Miner Metab. 2014. PMID: 23558979

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