Treffer 1 - 20 von 28 für Suche 'Jiang, Yu-wu', Suchdauer: 2,47s Treffer weiter einschränken
  1. 1
    Clinical and genetic characteristics of glucose transporter type 1 deficiency syndrome
    Weitere Verfasser: “...Jiang, Yu-wu...”
    Aufsatz

  2. 2
    Episodic central nervous system symptoms with reversible white matter involvement in Chinese patients with X-linked Charcot-Marie-Tooth disease and literatures review
    Weitere Verfasser: “...Jiang, Yu-wu...”
    Aufsatz

  3. 3
    Valproic acid-induced idiosyncratic liver injury in 4 cases
    Weitere Verfasser: “...Jiang, Yu-wu...”
    Aufsatz

  4. 4
    Clinical and genetic study of twelve Chinese patients with Alexander disease
    Weitere Verfasser: “...Jiang, Yu-wu...”
    Aufsatz

  5. 5
    Clinical and genetic analysis of a family with leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation
    Weitere Verfasser: “...Jiang, Yu-wu...”
    Aufsatz

  6. 6
    Analysis of HEPACAM mutations in a Chinese family with megalencephalic leukoencephalopathy with subcortical cysts
    Weitere Verfasser: “...Jiang, Yu-wu...”
    Aufsatz

  7. 7
    Emergency management of seizure and convulsive status epilepticus in children
    Aufsatz

  8. 8
    Electroclinical features of myoclonic-atonic epilepsy
    Weitere Verfasser: “...Jiang, Yu-wu...”
    Aufsatz

  9. 9
    Enzyme analysis of isolated mitochondrial respiratory chain complex III deficiency
    Weitere Verfasser: “...Jiang, Yu-wu...”
    Aufsatz

  10. 10
    Detection of vacuolated peripheral blood lymphocytes in screening for and diagnosis of lysosomal storage diseases
    Weitere Verfasser: “...Jiang, Yu-wu...”
    Aufsatz

  11. 11
    Advances in studies on molecular mechanisms underlying epileptogenesis
    Weitere Verfasser: “...Jiang, Yu-wu...”
    Aufsatz

  12. 12
    Clinical and electroencephalographic characteristics of epilepsy with myoclonic absences
    Weitere Verfasser: “...Jiang, Yu-wu...”
    Aufsatz

  13. 13
    Enhance neurogenetic etiologic studies actively and standardize diagnosis of neurodevelopmental disorders
    Aufsatz

  14. 14
    Clinical diagnosis and therapy of opsoclonus-myoclonus syndrome
    Weitere Verfasser: “...Jiang, Yu-wu...”
    Aufsatz

  15. 15
    Clinical features and management of multiple sclerosis in children
    Weitere Verfasser: “...Jiang, Yu-wu...”
    Aufsatz

  16. 16
    Clinical characteristics of cases with leukoencephalopathy with vanishing white matter
    Weitere Verfasser: “...Jiang, Yu-wu...”
    Aufsatz

  17. 17
    Detection of subtelomeric rearrangements in patients with idiopathic mental retardation/developmental delay
    Weitere Verfasser: “...Jiang, Yu-wu...”
    Aufsatz

  18. 18
    Clinical and genetic analysis of a family with Pelizaeus-Merzbacher disease
    Weitere Verfasser: “...Jiang, Yu-wu...”
    Aufsatz

  19. 19
    Clinical features and genotype-phenotype studies of 89 Chinese patients with X-linked adrenoleukodystrophy
    Weitere Verfasser: “...Jiang, Yu-wu...”
    Aufsatz

  20. 20
    Clinical studies on fifty-seven Chinese patients with combined methylmalonic aciduria and homocysteinemia
    Weitere Verfasser: “...Jiang, Yu-wu...”
    Aufsatz

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