Treffer 1 - 20 von 23 für Suche 'Bao, Xin-hua', Suchdauer: 6,89s Treffer weiter einschränken
  1. 1
    Clinical and genetic characteristics of glucose transporter type 1 deficiency syndrome
    Weitere Verfasser: “...Bao, Xin-hua...”
    Aufsatz

  2. 2
    Clinical, pathological and molecular biological characteristics of mitochondrial encephalomyopathy with lactic acidosis and stroke-like episode in children
    Weitere Verfasser: “...Bao, Xin-hua...”
    Aufsatz

  3. 3
    Valproic acid-induced idiosyncratic liver injury in 4 cases
    Weitere Verfasser: “...Bao, Xin-hua...”
    Aufsatz

  4. 4
    Electroclinical features of myoclonic-atonic epilepsy
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    Aufsatz

  5. 5
    Correlation between MECP2 genotype and phenotype in Chinese patients with Rett syndrome
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    Aufsatz

  6. 6
    Analysis of the parental origin of de novo MECP2 mutations and X chromosome inactivation in fifteen sporadic cases with Rett syndrome
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    Aufsatz

  7. 7
    Clinical and electrophysiologic studies on epileptic negative myoclonus in atypical benign partial epilepsy of childhood
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    Aufsatz

  8. 8
    Clinical diagnosis and therapy of opsoclonus-myoclonus syndrome
    Weitere Verfasser: “...Bao, Xin-hua...”
    Aufsatz

  9. 9
    Electroencephalogram characteristics of Rett syndrome
    Weitere Verfasser: “...Bao, Xin-hua...”
    Aufsatz

  10. 10
    Clinical features and genotype-phenotype studies of 89 Chinese patients with X-linked adrenoleukodystrophy
    Weitere Verfasser: “...Bao, Xin-hua...”
    Aufsatz

  11. 11
    Lovastatin induction of the redundant gene implications for therapy of X-linked adrenoleukodystrophy
    Weitere Verfasser: “...Bao, Xin-Hua...”
    Aufsatz

  12. 12
    Etiologic and clinical characteristics of syncope in children
    Weitere Verfasser: “...Bao, Xin-hua...”
    Aufsatz

  13. 13
    Diagnostic value of muscle, sural nerve and skin biopsies in childhood neuromuscular disorders
    Weitere Verfasser: “...Bao, Xin-hua...”
    Aufsatz

  14. 14
    Diagnosis of congenital muscular dystrophy and clinical significance of merosin expression
    Weitere Verfasser: “...Bao, Xin-hua...”
    Aufsatz

  15. 15
    MECP2 gene mutations in twenty-six cases with atypical Rett syndrome
    Weitere Verfasser: “...Bao, Xin-hua...”
    Aufsatz

  16. 16
    Clinical characteristics and long-term prognosis of Landau-Kleffner syndrome
    Weitere Verfasser: “...Bao, Xin-hua...”
    Aufsatz

  17. 17
    X chromosome inactivation patterns in patients with Rett syndrome and their mothers and the parental origin of the priority inactive X chromosome
    Weitere Verfasser: “...Bao, Xin-hua...”
    Aufsatz

  18. 18
    Screening for carrier and prenatal diagnosis of X-linked adrenoleukodystrophy
    Weitere Verfasser: “...Bao, Xin-hua...”
    Aufsatz

  19. 19
    Clinical and laboratory screening studies on urea cycle defects
    Weitere Verfasser: “...Bao, Xin-hua...”
    Aufsatz

  20. 20
    Clinical feature of Rett syndrome and MeCP2 genotype/phenotype correlation analysis
    Aufsatz

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