Case of a mentally retarded child with non-24 hour sleep-wake syndrome caused by deficiency of melatonin secretion

スポンサーリンク

概要

• 論文の詳細を見る
• 2000-06-01

著者

• TAKESHITA Kenzo

  Division of Child Neurology, Institute of Neurological Sciences, Faculty of Medicine, Tottori Univer

• AKABOSHI Shinjiro

  Division of Neurology, Iustitute of Neurological sciences, Faculty of Medicine, Tottori University

• Akaboshi Shinjiro

  Division Of Child Neurology Institute Of Neurological Sciences

• Takeshita Kenzo

  Division Of Child Neurology Institute Of Neurological Sciences

• Takeshita Kenzo

  Division Of Child Neurological Institute Of Neurology Sciences Faculty Of Medicine Tottori Universit

• INOUE YU-ICHI

  Department of Neuropsychiatry, Faculty of Medicine, Tottori University

• KUBOTA NORIKA

  Department of Paediatrics, Tottori Prefectural Kaike Rehabilitation Center for Disabled Children

• Inoue Yu-ichi

  Department Of Neuropsychiatry Faculty Of Medicine Tottori University

• Kubota Norika

  Department Of Paediatrics Tottori Prefectural Kaike Rehabilitation Center For Disabled Children

関連論文

• Diagnosis of Japanese patients with HHH syndrome by molecular genetic analysis : a common mutation, R179X
• Peroxisomal bifunctional enzyme deficiency: serial neurophysiological examinations of a case
• Epilepsy in Peroxisomal Diseases
• Genetic Heterogeneity of Niemann-Pick Disease Type C
• Accumulation of cholesterol and G_ ganglioside in cells cultured in the presence of progesterone:an implication for the basic defect in Niemann-Pick disease typc C
• Increased levels of GM_2 ganglioside in fibroblasts from a patient with juvenile Niemann - Pick disease type C
• Intracraninal calcifications, epilepsy, and optic atrophy associated with metaphyseal dysplasia: a case report
• Sensorineural deafness in siblings with adenosine deaminase deficiency
• A Cell Line Derived from Sphingomyelinosis Mouse Shows Alterations in Intracellular Cholesterol Metabolism Similar to Those in Type C Niemann-Pick Disease
• IgA and IgG2 Deficiency Associated with Zonisamide Therapy: A Case Report
• A functional magnetic resonance imaging study during sentence reading in Japanese dyslexic children
• Bile Aced Profiles in a Peroxisomal D-3-Hydroxyacyl-CoA Dehydratase/D-3-Hydroxyacyl-CoA Dehydrogenase Bifunctional Protein Deficiency
• Molecular epidemiology of C9 deficiency heterozygotes with an Arg95Stop mutation of the C9 gene in Japan
• Prenatal diagnosis of congenital myotonic dystrophy in two Japanese families: direct mutation analysis by a non-radioisotope PCR method and haplotype analysis with flanking DNA markers
• Cognitive and neurophysiological evaluation of Japanese dyslexia
• Frequency of the Prader-Willi syndrome in the San-in district, Japan
• Cellular senescence of angiofibroma stroma cells from patients with tuberous sclerosis
• Case of a mentally retarded child with non-24 hour sleep-wake syndrome caused by deficiency of melatonin secretion
• Slowly progressive cystic leukoencephalopathy with megalencephaly in a Japanese boy
• Carbohydrate-deficient glycoprotein syndrome : electrophoretic study of multiple serum glycoproteins
• Phosphory lated Sites of M_r 25,000 Protein, a Putative Protein Phosphatase 2A Modulator, and Phosphorylation of the Synthetic Peptide Containing These Sites by Protein Kinase C^1
• Pontine hypoplasia in a child with sensorineural deafiness
• Mutational analysis of TSC1 and TSC2 genes in Japanese patients with tuberous sclerosis complex
• Unilateral occlusion of the middle cerebral artery after varicella-zoster virus infection
• A patient with cerebral palsy whose mother had a traffic accident during pregnancy : a diffuse axonal injury?
• Non-radioactive DNA diagnosis for the fragile X syndrome in mentally retarded Japanese males
• Accumulation of GM2 Ganglioside in Niemann-Pick Disease Type C Fibroblasts
• Altered Sensitivities to Potential Inhibitors of Cholesterol Biosynthesis in Niemann-Pick Type C Fibroblasts
• A case report of remarkable improvement of motor disturbances with _L-dopa in a patient with post-diffuse axonal injury
• Studies on a Ca2+- and Cyclic Nucleotide-Independent H1 Histone Kinase Purified from Rabbit Skeletal Muscle
• Forced normalization induced by ethosuximide therapy in a patient with intractable myoclonic epilepsy
• Bilateral opercular syndrome: an unusyal complication of perinatal difficulties
• 一過性 Extreme Spindle を示した亜急性マイコプラスマ脳炎の一例
• Decreased resting energy expenditure in patients with Duchenne muscular dystrophy

もっと見る 閉じる

スポンサーリンク