H. Kaneko

发表

Sagittal plane deformity after temporary epiphysiodesis of the distal femur for correcting limb length discrepancy.

T. Hattori, K. Iwata, H. Furuhashi, 2020, Journal of orthopaedic science : official journal of the Japanese Orthopaedic Association.

Perhexiline maleate in the treatment of fibrodysplasia ossificans progressiva: an open-labeled clinical trial

K. Ohno, J. Horowitz, N. Ishiguro, 2013, Orphanet Journal of Rare Diseases.

Meclozine Facilitates Proliferation and Differentiation of Chondrocytes by Attenuating Abnormally Activated FGFR3 Signaling in Achondroplasia

A. Masuda, K. Ohno, Mikako Ito, 2013, PloS one.

Spondylometaphyseal dysplasia with cone‐rod dystrophy

Toshiyuki Yamamoto, M. Kondo, G. Nishimura, 2011, American journal of medical genetics. Part A.

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

N. Ishiguro, H. Kitoh, K. Mishima, 2012, Molecular Syndromology.

Guided growth for coronal lower limb deformities in skeletal dysplasia

H. Kitoh, K. Mishima, M. Matsushita, 2022, Journal of pediatric orthopedics. Part B.

A retrospective comparative study of corrective osteotomy for tibial deformities with the multiaxial correction fixator and the circular fixator.

N. Ishiguro, H. Kitoh, K. Mishima, 2020, Journal of clinical orthopaedics and trauma.

A retrospective comparative study of corrective osteotomy for tibial deformities with the multiaxial correction ﬁ xator and the circular Journal of Clinical Orthopaedics and Trauma

H. Kitoh, K. Mishima, M. Matsushita, 2022 .

Differential Effects of Culture-expanded Bone Marrow Cells on the Regeneration of Bone Between the Femoral and the Tibial Lengthenings

N. Ishiguro, H. Kitoh, H. Kaneko, 2009, Journal of pediatric orthopedics.

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

N. Ishiguro, H. Kitoh, Y. Tokita, 2013, Journal of Bone and Mineral Metabolism.

Isolated bifid rib: Clinical and radiological findings in children

N. Ishiguro, H. Kitoh, K. Mishima, 2012, Pediatrics international : official journal of the Japan Pediatric Society.

Scurvy as a differential diagnosis of diffuse musculoskeletal pain in children: Two case reports

H. Kitoh, Akiko Kitamura, H. Kaneko, 2022, JOS Case Reports.

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

A. Masuda, K. Ohno, F. Rauch, 2011, Human Genetics.

Long-term Outcome of Gradual Reduction Using Overhead Traction for Developmental Dysplasia of the Hip Over 6 Months of Age

N. Ishiguro, H. Kitoh, K. Mishima, 2013, Journal of pediatric orthopedics.

Radiographic Analysis of Movements of the Acetabulum and the Femoral Head After Salter Innominate Osteotomy

N. Ishiguro, H. Kitoh, H. Kaneko, 2009, Journal of pediatric orthopedics.

Docking phenomenon and subsequent acetabular development after gradual reduction using overhead traction for developmental dysplasia of the hip over six months of age

H. Kitoh, T. Hattori, Akiko Kitamura, 2021, Journal of children's orthopaedics.

Appropriate Surgical Timing of Salter Innominate Osteotomy for Residual Acetabular Dysplasia in Children

H. Kitoh, T. Hattori, Akiko Kitamura, 2022, Journal of pediatric orthopedics.

A comparative study of blade plate fixation and external fixation in osteotomies for slipped capital femoral epiphysis

N. Ishiguro, H. Kitoh, T. Kitakoji, 2013, Journal of pediatric orthopedics. Part B.

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?

N. Ishiguro, H. Kitoh, K. Mishima, 2014, The bone & joint journal.

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

N. Ishiguro, H. Kitoh, K. Mishima, 2013, Journal of pediatric orthopedics. Part B.

A novel SOX9 H169Q mutation in a family with overlapping phenotype of mild campomelic dysplasia and small patella syndrome

G. Nishimura, N. Ishiguro, H. Kitoh, 2013, American journal of medical genetics. Part A.

Two children with hypophosphatasia with a heterozygous c.1559delT variant in the ALPL gene, the most common variant in Japanese populations

T. Ogi, H. Kitoh, Akiko Kitamura, 2022, Bone Reports.

Femoral lengthening with enzyme replacement therapy in an adolescent patient with prenatal benign hypophosphatasia: A case report.

H. Kitoh, Akiko Kitamura, H. Kaneko, 2021, Journal of orthopaedic science : official journal of the Japanese Orthopaedic Association.

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

N. Ishiguro, H. Kitoh, T. Katagiri, 2011, The Journal of bone and joint surgery. American volume.

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

N. Ishiguro, H. Kitoh, Y. Nishida, 2012, Journal of pediatric orthopedics. Part B.

Changes of the lower limb deformity in children with FGF23-related hypophosphatemic rickets treated with Burosumab: a single-center prospective study.

H. Kitoh, T. Hamajima, Akiko Kitamura, 2022, Journal of pediatric orthopedics. Part B.

Prognostic factors for mobility in children with osteogenesis imperfecta.

H. Kitoh, T. Hattori, Akiko Kitamura, 2022, Medicine.

Comparison of surgical and nonsurgical containment methods for patients with Legg-Calvé-Perthes disease of the onset ages between 6.0 and 8.0 years: Salter osteotomy versus a non-weight-bearing hip flexion-abduction brace

N. Ishiguro, H. Kitoh, K. Mishima, 2019, Journal of pediatric orthopedics. Part B.