Abnormalities of voluntary saccades in Gilles de la Tourette's syndrome : pathophysiological consideration

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概要

• 論文の詳細を見る
• 2003-12-01

著者

• Nomura Yoshiko

  Segawa Neurological Clinic For Children

• FUKUDA Hideki

  National Institute of Industrial Health

• TERAO Yasuo

  Tokyo University, Department of Neurology

• HIKOSAKA Okihide

  National Eye Institute, National Institute of Health

• SEGAWA Masaya

  Segawa Neurological Clinic for Children

• Terao Yasuo

  Tokyo University Department Of Neurology

• Hikosaka Okihide

  National Eye Institute National Institute Of Health

• Nomura Yoshiko

  Segawa Neurologic Clinic For Children

• Segawa Masaya

  Segawa Neurologic Clinic For Children

関連論文

• Abnormalities of voluntary saccades in Gilles de la Tourette's syndrome : pathophysiological consideration
• A missense mutation in SCN1A in brothers with severe myoclonic epilepsy in infancy (SMEI) inherited from a father with febrile seizures
• Neurology of Tourette's syndrome (TS) TS as a developmental dopamine disorder : a hypothesis
• Guidelines for reporting clinical features in cases with MECP2 mutations
• Gene mutation in hereditary progressive dystonia with marked diurnal fluctuation(HPD), strictly defined dopa-responsive dystonia
• X-ray induced Sister Chromatid Exchange and Chromosomal Aberrations in the Lymphocytes from the Patients with Neurofibromatosis
• Two phenotypes and anticipation observed in Japanese cases with early onset torsion dystonia(DYT1) : pathophysiological consideration
• Emerging and entraining patterns of the sleep-wake rhythm in preterm and term infants
• R133C and R168X mutations in Japanese Rett syndrome patients : a caution for misdiagnosis
• Mutational analysis of the MECP2 gene in Japanese patients with Rett syndrome
• Development of the nigrostriatal dopamine neuron and the pathways in the basal ganglia
• Neurophysiology of Tourette's syndrome : pathophysiological considerations
• Video analysis of gross body movements during sleep
• Preface
• Hereditary progressive dystonia with marked diurnal fluctuation
• Cases of dopa-responsive dystonia (Segawa disease) in Estonia
• Guidelines for reporting clinical features in cases with MECP2 mutations, by Alison Kerr and an international group
• Nurses' workload associated with 16-h night shifts. II : Effects of a nap taken during the shifts
• Nurses' workload associated with 16-h night shifts on the 2-shift system. I : Comparison with the 3-shift system
• Early behavior characteristics and sleep disturbance in Rett syndrome
• Functional analyses of MeCP2 mutations associated with Rett syndrome using transient expression systems
• Neurophysiology of Rett syndrome
• 1-3 Enhancement of Cold-induced Vasodilatation Responses During and Following Physical Exercise in Moderate Cold Environments(Proceedings of the 53rd Meeting of Japan Society of Physiological Anthropology)
• Development of language in Rett syndrome
• Early motor disturbances in Rett syndrome and its pathophysiological importance
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• Pathophysiology of Rett syndrome from the stand point of clinical
• Hereditary progressive dystonia with marked diurnal fluctuation
• Frequencies of sister chromatid exchanges in cells from patients with neurofibromatosis induced by mitomycin-C.
• S-602 Effect of Physical Exercise before and during Finger Cooling on Cold-Induced Vasodilatation (CIVD) Reactivity and Subjective Thermal Strain in a Moderate Cold Environment

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