Kondo Naomi | College Of Agriculture And Veterinary Medicine Nihon University

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著作論文

ムコ多糖症2型患者とその家族の精神心理学的検討
Parents of childhood X-linked adrenoleukodystrophy : High risk for depression and neurosis
Evaluation of ADL in patients with Hunter disease using FIM score
Aberrant peroxisome morphology in peroxisomal beta-oxidation enzyme deficiencies
Autoantibodies and Cell-mediated Autoimmunity to NMDA-type GluRε2 in Patients with Rasmussen's Encephalitis and Chronic Progressive Epilepsia Partialis Continua
Gas chromatography/mass spectrometry analysis of very long chain fatty acids, docosahexaenoic acid, phytanic acid and plasmalogen for the screening of peroxisomal disorders
Epidemiology of X-linked adrenoleukodystrophy in Japan
III C1 Probable molecular dysfunction by autoantibodies against NMDA receptor GluRe2 in epilepsies after acute encephalitis
Urinary organic acids in peroxisomal disorders : a simple screening method
Epileptic seizures and structural abnormalities in a patient with holoprosencephaly
The peroxin Pex6p gene is impaired in peroxisomal biogenesis disorders of complementation group 6
The clinical course of childhood and adolescent adrenoleukodystrophy before and after Lorenzo's oil
Congenital myotonic dystrophy : report of paternal transmission
Restoration of biochemical function of the peroxisome in the temperature-sensitive mild forms of peroxisome biogenesis disorder in humans
Prenatal diagnosis of peroxisomal d-3-hydroxyacyl-CoA dehydratase / d-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiency
A novel nonsense mutation of the PEX7 gene in a patient with rhizomelic chondrodysplasia punctata
Two different pathological conditions of photoparoxysmal responses in hereditary dentatorubral-pallidoluysian atrophy
Epilepsy in Peroxisomal Diseases
Trial of docosahexaenoic acid supplementation on a Japanese patient with a peroxisome biogenesis defect
Various Expression Patterns of α1 and α2 Genes in IgA Deficiency
Age-Related Changes of Transforming Growth Factor β1 in Japanese Children
病原性大腸菌O-157による溶血性尿毒症症候群における中枢神経系障害の出現の予測のために役に立つ指標(SCWPスコア)
Expression, Purification and Structural Analysis of Human IL-18 Binding Protein : A Potent Therapeutic Molecule for Allergy
Hypothermia Augments NF-kappaB Activity and the Production of IL-12 and IFN-gamma
Clinical and bacteriological evaluation of the efficacy of piperacillin in children with pneumonia
Pharmacokinetics of Beclomethasone Dipropionate in an Hydrofluoroalkane-134a Propellant System in Japanese Children with Bronchial Asthma
Development of Fluorescence-linked Immunosorbent Assay for High Throughput Screening of Interferon-γ
Questionnaire-based Study on the Relationship between Pet-keeping and Allergic Diseases in Young Children in Japan
Urinary leukotriene E_4 and 11-dehydro-thromboxane B_2 excretion in children with bronchial asthma
Genetic defects in downregulation of IgE production and a new genetic classification of atopy
Population pharmacokinetics of pranlukast hydrate dry syrup in children with bronchial asthma
Interleukin-18 is associated with the severity of atopic dermatitis
Development of Morquio A Mice and Enzyme Replacement Therapy
Toward a new treatment : Role of International Morquio Registry
A New Approach to Develop Mice Model
Spectrums of Mutations in Mucopolysaccharidosis IVA (Morquio disease) gene
MUCOPOLYSACCHARIDOSIS IVA : A NOVEL SPLICE ACCEPTOR SITE MUTATION IN INTRON 4 OF THE N-ACETYLGALACTOSAMINE-6-SULFATE SULFATASE GENE IN AN AFGHANISTAN GIRL WITH CLASSICAL MORQUIO DISEASE
Carnitine Palmitoyltransferase 2 Deficiency : The Time-Course of Blood and Urinary Acylcarnitine Levels during Initial L-Carnitine Supplementation
Biochemical and Immunocytochemical Properties of Peroxisomes and Mitochondria in Bovine Chromaffin Cells
Prediction of the pathogenesis of the mutation in MeCP2 C-terminal domain
Pure Isolation of a New Chemoautotrophic Ammonia-Oxidizing Bacterium on Cellan Gum Plate

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