Nobuhiko Haga

Summary

Affiliation: University of Tokyo
Country: Japan

Publications

  1. ncbi request reprint Effect of rehabilitation on mortality of patients with Guillain-Barre Syndrome: a propensity-matched analysis using nationwide database
    H Inokuchi
    Department of Rehabilitation Medicine Graduate School of Medicine, The University of Tokyo, Tokyo, Japan
    Eur J Phys Rehabil Med 50:439-46. 2014
  2. doi request reprint Education and related support from medical specialists for Japanese patients with major skeletal dysplasias
    Nobuhiko Haga
    Department of Rehabilitation Medicine, The University of Tokyo Hospital, 7 3 1 Hongo, Bunkyo ku, Tokyo 113 8655, Japan Electronic address
    Disabil Health J 6:399-404. 2013
  3. doi request reprint Epidemiology of hereditary sensory and autonomic neuropathy type IV and V in Japan
    Nobuhiko Haga
    Department of Rehabilitation Medicine, The University of Tokyo, Tokyo, Japan
    Am J Med Genet A 161:871-4. 2013
  4. doi request reprint Successful ambulation by surgical conversion in a complex form of epigastric heteropagus
    Nobuhiko Haga
    Departments of Rehabilitation Medicine, The University of Tokyo Hospital, Tokyo, Japan
    J Pediatr Orthop B 18:394-6. 2009
  5. ncbi request reprint Osteochondral destruction in the hand following bee stings: a case report of an infant
    Nobuhiko Haga
    Department of Pediatric Orthopedics, Shizuoka Children s Hospital, Shizuoka City, Shizuoka 420 8660, Japan
    Hand Surg 11:143-5. 2006
  6. ncbi request reprint Novel COL9A3 mutation in a family with multiple epiphyseal dysplasia
    Eiji Nakashima
    Laboratory for Bone and Joint Diseases, SNP Research Center, RIKEN, Tokyo, Japan
    Am J Med Genet A 132:181-4. 2005
  7. ncbi request reprint The phenotypic spectrum of COL2A1 mutations
    Gen Nishimura
    Department of Radiology, Tokyo Metropolitan Kiyose Children s Hospital, Tokyo, Japan
    Hum Mutat 26:36-43. 2005
  8. ncbi request reprint Circulating COMP is decreased in pseudoachondroplasia and multiple epiphyseal dysplasia patients carrying COMP mutations
    Akihiko Mabuchi
    Laboratory for Bone and Joint Diseases, SNP Research Center, RIKEN, Tokyo, Japan
    Am J Med Genet A 129:35-8. 2004
  9. ncbi request reprint Novel 3-dimensional motion analysis method for measuring the lumbar spine range of motion: repeatability and reliability compared with an electrogoniometer
    Michio Tojima
    Department of Rehabilitation Medicine, The University of Tokyo, Tokyo, Japan Department of Rehabilitation Medicine, The University of Tokyo Hospital, Japan Department of Sensory Recognition and Locomotive Function Sciences in the Super Aged Society, The University of Tokyo, Tokyo, Japan and Department of Medical Engineering, The University of Tokyo Hospital, Tokyo, Japan
    Spine (Phila Pa 1976) 38:E1327-33. 2013
  10. ncbi request reprint Bizarre presentation of epigastric heteropagus: report of a case
    Yutaka Kanamori
    Departments of Pediatric Surgery, The University of Tokyo Hospital, 7 3 1 Hongo, Tokyo 113 8655, Japan
    Surg Today 36:914-8. 2006

Collaborators

Detail Information

Publications29

  1. ncbi request reprint Effect of rehabilitation on mortality of patients with Guillain-Barre Syndrome: a propensity-matched analysis using nationwide database
    H Inokuchi
    Department of Rehabilitation Medicine Graduate School of Medicine, The University of Tokyo, Tokyo, Japan
    Eur J Phys Rehabil Med 50:439-46. 2014
    ..Rehabilitation for patients with Guillain-Barre Syndrome (GBS) is recommended as it improves the outcome of neurological deficits. Few studies focused on the effect of rehabilitation on mortality of the patients...
  2. doi request reprint Education and related support from medical specialists for Japanese patients with major skeletal dysplasias
    Nobuhiko Haga
    Department of Rehabilitation Medicine, The University of Tokyo Hospital, 7 3 1 Hongo, Bunkyo ku, Tokyo 113 8655, Japan Electronic address
    Disabil Health J 6:399-404. 2013
    ..Though necessary support in education is presumed to differ among patients with different disorders, few articles report on education in patients with skeletal dysplasias...
  3. doi request reprint Epidemiology of hereditary sensory and autonomic neuropathy type IV and V in Japan
    Nobuhiko Haga
    Department of Rehabilitation Medicine, The University of Tokyo, Tokyo, Japan
    Am J Med Genet A 161:871-4. 2013
    ..Most patients with HSAN-IV were 5-40 years of age, whereas half of the patients with HSAN-V were 40 years or older...
  4. doi request reprint Successful ambulation by surgical conversion in a complex form of epigastric heteropagus
    Nobuhiko Haga
    Departments of Rehabilitation Medicine, The University of Tokyo Hospital, Tokyo, Japan
    J Pediatr Orthop B 18:394-6. 2009
    ..At the age of 4, we performed the subtrochanteric femoral osteotomy with 90 degrees of varization and rotation, along with knee disarticulation. Ambulation was successfully achieved with the prosthesis with a multiaxis knee unit...
  5. ncbi request reprint Osteochondral destruction in the hand following bee stings: a case report of an infant
    Nobuhiko Haga
    Department of Pediatric Orthopedics, Shizuoka Children s Hospital, Shizuoka City, Shizuoka 420 8660, Japan
    Hand Surg 11:143-5. 2006
    ..The clinical findings resembled those reported as "beekeeper's arthropathy", but the radiological findings were more severe. Histology of the resected specimen revealed fibrous granulation tissue with infiltration of inflammation cells...
  6. ncbi request reprint Novel COL9A3 mutation in a family with multiple epiphyseal dysplasia
    Eiji Nakashima
    Laboratory for Bone and Joint Diseases, SNP Research Center, RIKEN, Tokyo, Japan
    Am J Med Genet A 132:181-4. 2005
    ..The radiographic phenotypes of the patients were relatively milder than those of previously reported cases, and were indistinguishable to common, idiopathic OA...
  7. ncbi request reprint The phenotypic spectrum of COL2A1 mutations
    Gen Nishimura
    Department of Radiology, Tokyo Metropolitan Kiyose Children s Hospital, Tokyo, Japan
    Hum Mutat 26:36-43. 2005
    ..All six C-propeptide mutations produced a range of atypical skeletal phenotypes and created ocular, but not otolaryngological, changes...
  8. ncbi request reprint Circulating COMP is decreased in pseudoachondroplasia and multiple epiphyseal dysplasia patients carrying COMP mutations
    Akihiko Mabuchi
    Laboratory for Bone and Joint Diseases, SNP Research Center, RIKEN, Tokyo, Japan
    Am J Med Genet A 129:35-8. 2004
    ..001). Our results indicate that circulating COMP levels reflect genetic abnormalities in COMP, providing an easier, more rapid and cost-efficient method for diagnosing PSACH and particularly for MED...
  9. ncbi request reprint Novel 3-dimensional motion analysis method for measuring the lumbar spine range of motion: repeatability and reliability compared with an electrogoniometer
    Michio Tojima
    Department of Rehabilitation Medicine, The University of Tokyo, Tokyo, Japan Department of Rehabilitation Medicine, The University of Tokyo Hospital, Japan Department of Sensory Recognition and Locomotive Function Sciences in the Super Aged Society, The University of Tokyo, Tokyo, Japan and Department of Medical Engineering, The University of Tokyo Hospital, Tokyo, Japan
    Spine (Phila Pa 1976) 38:E1327-33. 2013
    ..Repeatability and reliability for measuring methods for real-time lumbar range of motion...
  10. ncbi request reprint Bizarre presentation of epigastric heteropagus: report of a case
    Yutaka Kanamori
    Departments of Pediatric Surgery, The University of Tokyo Hospital, 7 3 1 Hongo, Tokyo 113 8655, Japan
    Surg Today 36:914-8. 2006
    ....
  11. ncbi request reprint The ACVR1 617G>A mutation is also recurrent in three Japanese patients with fibrodysplasia ossificans progressiva
    Masahiro Nakajima
    Laboratory for Bone and Joint Diseases, SNP Research Center, RIKEN, 4 6 1 Shirokanedai, Minato ku, Tokyo, 108 8639, Japan
    J Hum Genet 52:473-5. 2007
    ..Here, we examined three Japanese patients with FOP for ACVR1 mutations. We identified the 617G>A mutation in all three patients. Our results suggest that the mutation in the ACVR1 gene is common and recurrent in the global population...
  12. ncbi request reprint Two-dimensional video gait analyses in patients with congenital insensitivity to pain
    Yasu Zhang
    Department of Rehabilitation Medicine, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan
    Dev Neurorehabil 16:266-70. 2013
    ..To clarify the features of gait in patients with congenital insensitivity to pain (CIP) by analyzing the video-recorded gait...
  13. doi request reprint Characteristic factors of ankle valgus with multiple cartilaginous exostoses
    Kazuharu Takikawa
    Department of Pediatric Orthopedics, Shizuoka Children s Hospital, Shizuoka, Japan
    J Pediatr Orthop 28:761-5. 2008
    ..Ankle valgus is one of the most common deformities in multiple cartilaginous exostoses (MCEs). However, the characteristic factors of ankle valgus are not well known...
  14. doi request reprint Evaluation of postural control in quiet standing using center of mass acceleration: comparison among the young, the elderly, and people with stroke
    Erkang Yu
    Department of Rehabilitation Medicine, Graduate School of Medicine, The University of Tokyo, Bunkyo ku, Tokyo, Japan
    Arch Phys Med Rehabil 89:1133-9. 2008
    ..To determine center of mass (COM) acceleration usefulness in the evaluation of postural control during quiet standing...
  15. ncbi request reprint Treatment of congenital pseudarthrosis of the tibia: a multicenter study in Japan
    Isao Ohnishi
    Department of Pediatric Orthopaedics, Shizuoka Children s Hospital, Shizuoka, Japan
    J Pediatr Orthop 25:219-24. 2005
    ..According to the results of this study, the most acceptable methods of treatment of CPT are the Ilizarov method and the vascularized fibular graft...
  16. doi request reprint An open trial of long-term testosterone suppression in spinal and bulbar muscular atrophy
    Tomotaka Yamamoto
    Department of Neurology, The University of Tokyo Hospital, 7 3 1 Hongo, Bunkyo ku, Tokyo, 113 8655, Japan
    Muscle Nerve 47:816-22. 2013
    ..We investigated the long-term effects of leuprorelin on leg-muscle strength in spinal and bulbar muscular atrophy (SBMA). We hypothesized that testosterone suppression by leuprorelin would prevent the progression of muscle weakness...
  17. ncbi request reprint Evaluating visual bias and effect of proprioceptive feedback in unilateral neglect
    Yu Chiba
    Department of Rehabilitation Medicine, The University of Tokyo Hospital, 7 3 1 Hongo, Bunkyo, Tokyo 113 0033, Japan
    J Clin Neurosci 17:1148-52. 2010
    ..Visual bias and effect of proprioceptive feedback in unilateral neglect were successfully assessed by these tasks...
  18. ncbi request reprint Recurrent salmonella osteomyelitis of both hands in a child with no signs of haemoglobinopathy: follow-up until 19 years of age
    Nobuhiko Haga
    Department of Pediatric Orthopedics, Shizuoka Children s Hospital, Shizuoka, Japan
    Scand J Plast Reconstr Surg Hand Surg 37:315-7. 2003
    ..She was not affected by sickle cell disease, which sometimes accompanies acute swelling of hands and feet, and is known as hand-foot syndrome...
  19. ncbi request reprint Effects of passive leg movement on the oxygenation level of lower limb muscle in chronic stroke patients
    Enkhsaihan Jigjid
    Department of Rehabilitation Medicine, Graduate School of Medicine, University of Tokyo, Tokyo, Japan
    Neurorehabil Neural Repair 22:40-9. 2008
    ..To evaluate the effects of passive leg movements on the muscle oxygenation level and electromyographic (EMG) activity in the lower limbs in chronic stroke patients...
  20. ncbi request reprint Spine and rib abnormalities and stature in spondylocostal dysostosis
    Kazuharu Takikawa
    Department of Pediatric Orthopedics, Shizuoka Children s Hospital, Shizuoka City, Japan
    Spine (Phila Pa 1976) 31:E192-7. 2006
    ..A retrospective study of radiographic and clinical findings of spondylocostal dysostosis...
  21. doi request reprint Evaluation of nonnociceptive sensation in patients with congenital insensitivity to pain with anhidrosis
    Masahiro Iijima
    Department of Rehabilitation Medicine, Graduate School of Medicine, The University of Tokyo, 7 3 1 Hongo, Bunkyo ku, Tokyo 113 8655, Japan
    Childs Nerv Syst 26:1085-9. 2010
    ..The aim of this study was to evaluate peripheral sensory nerve function, including senses of touch/pressure, vibration, joint position, and two-point discrimination, in patients with CIPA by basic clinical neurological examination...
  22. doi request reprint Analysing non-motor bias in unilateral neglect with a new variant of the line bisection task
    Yu Chiba
    Department of Rehabilitation Medicine, The University of Tokyo Hospital, Japan
    Brain Inj 22:952-9. 2008
    ..To develop a new variant of the line-bisection task for assessing non-motor (attentional, representational, etc.) bias in unilateral neglect (UN), i.e. the exactly bisected line selection task (EBLST)...
  23. ncbi request reprint Novel types of COMP mutations and genotype-phenotype association in pseudoachondroplasia and multiple epiphyseal dysplasia
    Akihiko Mabuchi
    Laboratory for Bone and Joint Deseases, SNP Research Center, RIKEN, c o Institute of Medical Science, University of Tokyo, Tokyo, Japan
    Hum Genet 112:84-90. 2003
    ..0024). These findings expand the mutation spectrum of the COMP gene and highlight genotype-phenotype relationships, facilitating improved genetic diagnosis and analysis of COMP function in humans...
  24. ncbi request reprint Management of disabilities associated with achondroplasia
    Nobuhiko Haga
    Department of Pediatric Orthopedics, Shizuoka Children s Hospital, 860 Urushiyama, Shizuoka 420 8660, Japan
    J Orthop Sci 9:103-7. 2004
    ..When managing patients, orthopedists should consider the overall aspects of achondroplasia, including natural development and complications other than orthopedic factors...
  25. doi request reprint Vertical peak ground force in human infant crawling
    Arito Yozu
    Department of Rehabilitation Medicine, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan
    Gait Posture 37:293-5. 2013
    ..638±0.089 (per BW). No significant difference was observed between FL and HL Vpk. The mean FL/HL Vpk ratio was -0.011 on a natural logarithmic scale. These data could be added to the current database on Vpk for quadrupedalism...
  26. doi request reprint Facial morphology and occlusion of a patient with fibrodysplasia ossificans progressiva (FOP): a case report
    Takafumi Susami
    Department of Oral Maxillofacial Surgery, Dentistry and Orthodontics, The University of Tokyo Hospital, Tokyo, Japan
    Spec Care Dentist 32:165-70. 2012
    ..His mandible rotated in a counterclockwise direction. His molars had delayed eruption or were impacted and seven were extracted. His mouth opening increased slightly and his oral hygiene improved to excellent...
  27. ncbi request reprint Slipped capital femoral epiphysis following contralateral infantile Blount's disease
    Kazuharu Takikawa
    Department of Pediatric Orthopedics, Shizuoka Children s Hospital, 860 Urushiyama, Shizuoka 420 8860, Japan
    J Orthop Sci 7:403-4. 2002
    ..In this patient, pelvic tilt caused by leg length discrepancy associated with infantile Blount's disease and possible general weakness of the growth plate may be related to the occurrence of SCFE...
  28. ncbi request reprint Novel and recurrent mutations clustered in the von Willebrand factor A domain of MATN3 in multiple epiphyseal dysplasia
    Akihiko Mabuchi
    Laboratory for Bone and Joint Diseases, SNP Research Center, RIKEN, 108 8639 Tokyo, Japan
    Hum Mutat 24:439-40. 2004
    ..120-127). Contrary to the previous assumption that the MATN3 mutation in MED is confined to the beta-sheet regions, one novel mutation (p.F105S) is located outside the beta-sheet region, within an alpha-helix region...
  29. ncbi request reprint Comprehensive screening of multiple epiphyseal dysplasia mutations in Japanese population
    Taichi Itoh
    Center for Molecular Biology and Cytogenetics, SRL Inc, Hino, Japan
    Am J Med Genet A 140:1280-4. 2006
    ..Based on the integration of clinical and genetic information, we propose an algorithm for detecting mutations in Japanese MED patients. Our study further supports the existence of additional MED gene(s)...