Treffer 1 - 20 von 21 für Suche 'Qiu, Wen-juan', Suchdauer: 2,84s Treffer weiter einschränken
  1. 1
    Outcomes of patients with combined methylmalonic acidemia and homocystinuria after treatment
    Weitere Verfasser: “...Qiu, Wen-juan...”
    Aufsatz

  2. 2
    Analysis of GALNS gene mutation in thirty-eight Chinese patients with mucopolysaccharidosis type IVA
    Weitere Verfasser: “...Qiu, Wen-juan...”
    Aufsatz

  3. 3
    Application of succinylacetone levels measurement in the blood and urine in the diagnosis of tyrosinemia type 1
    Weitere Verfasser: “...Qiu, Wen-juan...”
    Aufsatz

  4. 4
    GLB1 gene mutation and clinical characteristics of a patient with mucopolysaccharidosis type IVB
    Weitere Verfasser: “...Qiu, Wen-juan...”
    Aufsatz

  5. 5
    Primary carnitine deficiency in 17 patients diagnosis, treatment and follow up
    Weitere Verfasser: “...Qiu, Wen-juan...”
    Aufsatz

  6. 6
    Comparison and clinical application of two methods for determination of plasma chitotriosidase activity
    Weitere Verfasser: “...Qiu, Wen-juan...”
    Aufsatz

  7. 7
    Pay attention to etiologic diagnosis of cardiomyopathy in children
    Weitere Verfasser: “...Qiu, Wen-juan...”
    Aufsatz

  8. 8
    Establishment and clinical application of dried blood spots and mixed leukocytes for determination of acid alpha-glucosidase activity
    Aufsatz

  9. 9
    Clinical diagnosis and WISP3 gene mutation analysis for progressive pseudorheumatoid dysplasia
    Weitere Verfasser: “...Qiu, Wen-juan...”
    Aufsatz

  10. 10
    Enzymatic diagnosis of 47 cases with mucopolysaccharidosis
    Weitere Verfasser: “...Qiu, Wen-Juan...”
    Aufsatz

  11. 11
    Analysis of gene mutations in Chinese patients with methylmalonic acidemia and homocysteinemia
    Weitere Verfasser: “...Qiu, Wen-juan...”
    Aufsatz

  12. 12
    Molecular genetic analysis of 10 Chinese patients with glycogen storage disease type III
    Weitere Verfasser: “...Qiu, Wen-juan...”
    Aufsatz

  13. 13
    Diagnosis, treatment and gene mutation analysis of the first case with dihydropteridine reductase deficiency in the mainland of China
    Weitere Verfasser: “...Qiu, Wen-juan...”
    Aufsatz

  14. 14
    Gene mutation analysis in patients with propionic acidemia
    Weitere Verfasser: “...Qiu, Wen-juan...”
    Aufsatz

  15. 15
    Clinical and mutational study of a Chinese infant with isovaleric acidemia
    Aufsatz

  16. 16
    Values of tandem mass spectrometry in etiologic diagnosis of cerebral developmental retardation
    Weitere Verfasser: “...Qiu, Wen-juan...”
    Aufsatz

  17. 17
    Application of tandem mass spectrometry in diagnosis of organic acidemias
    Weitere Verfasser: “...Qiu, Wen-juan...”
    Aufsatz

  18. 18
    Screening and diagnosis of tetrahydrobiopterin responsive phenylalanine hydroxylase deficiency with tetrahydrobiopterin loading test
    Weitere Verfasser: “...Qiu, Wen-juan...”
    Aufsatz

  19. 19
    Molecular genetic analysis of congenital lipoid adrenal hyperplasia
    Aufsatz

  20. 20
    A discussion on risk factors of final height in 21-hydroxylase deficiency patients
    Weitere Verfasser: “...Qiu, Wen-juan...”
    Aufsatz

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