SEGAWA Masaya | Segawa Neurological Clinic for Children

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著作論文

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
Functional analyses of MeCP2 mutations associated with Rett syndrome using transient expression systems
Development of language in Rett syndrome
Epilepsy in autism : A pathophysiological consideration

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