Treffer 1 - 20 von 27 für Suche 'Qiu, Wen', Suchdauer: 1,77s Treffer weiter einschränken
  1. 1
    A novel inherited CARD9 deficiency in an otherwise healthy woman with CNS candidiasis
    von Zhou, Ling-Hong
    Veröffentlicht in: Clinical immunology (Orlando, Fla.) (2024)
    Weitere Verfasser: “...Qiu, Wen-Jia...”

    Online-Aufsatz

  2. 2
    Enhancing anaerobic digestion of sulphate wastewater by adding nano-zero valent iron
    von Liu, Jiacheng
    Veröffentlicht in: Environmental technology (2023)
    Weitere Verfasser: “...Qiu, Wen...”

    Online-Aufsatz

  3. 3
    Surface Deposition of Juglone/FeIII on Microporous Membranes for Oil/Water Separation and Dye Adsorption
    Weitere Verfasser: “...Qiu, Wen-Ze...”

    Online-Aufsatz

  4. 4
    Virus-Inspired Nanogenes Free from Man-Made Materials for Host-Specific Transfection and Bio-Aided MR Imaging
    Weitere Verfasser: “...Qiu, Wen-Xiu...”

    Online-Aufsatz

  5. 5
    Overexpression of the CsFUS3 gene encoding a B3 transcription factor promotes somatic embryogenesis in Citrus
    Weitere Verfasser: “...Qiu, Wen-Ming...”

    Online-Aufsatz

  6. 6
    Relationship between Insulin Levels and Nonpsychotic Dementia A Systematic Review and Meta-Analysis
    von Pan, Qiu-Xia
    Veröffentlicht in: Neural plasticity (2017)
    Weitere Verfasser: “...Qiu, Wen-Qi...”

    Online-Aufsatz

  7. 7
    Analysis of GALNS gene mutation in thirty-eight Chinese patients with mucopolysaccharidosis type IVA
    Weitere Verfasser: “...Qiu, Wen-juan...”
    Aufsatz

  8. 8
    Outcomes of patients with combined methylmalonic acidemia and homocystinuria after treatment
    Weitere Verfasser: “...Qiu, Wen-juan...”
    Aufsatz

  9. 9
    Comparison and clinical application of two methods for determination of plasma chitotriosidase activity
    Weitere Verfasser: “...Qiu, Wen-juan...”
    Aufsatz

  10. 10
    Application of succinylacetone levels measurement in the blood and urine in the diagnosis of tyrosinemia type 1
    Weitere Verfasser: “...Qiu, Wen-juan...”
    Aufsatz

  11. 11
    GLB1 gene mutation and clinical characteristics of a patient with mucopolysaccharidosis type IVB
    Weitere Verfasser: “...Qiu, Wen-juan...”
    Aufsatz

  12. 12
    Primary carnitine deficiency in 17 patients diagnosis, treatment and follow up
    Weitere Verfasser: “...Qiu, Wen-juan...”
    Aufsatz

  13. 13
    Clinical diagnosis and WISP3 gene mutation analysis for progressive pseudorheumatoid dysplasia
    Weitere Verfasser: “...Qiu, Wen-juan...”
    Aufsatz

  14. 14
    Pay attention to etiologic diagnosis of cardiomyopathy in children
    Weitere Verfasser: “...Qiu, Wen-juan...”
    Aufsatz

  15. 15
    Establishment and clinical application of dried blood spots and mixed leukocytes for determination of acid alpha-glucosidase activity
    Aufsatz

  16. 16
    Enzymatic diagnosis of 47 cases with mucopolysaccharidosis
    Weitere Verfasser: “...Qiu, Wen-Juan...”
    Aufsatz

  17. 17
    Analysis of gene mutations in Chinese patients with methylmalonic acidemia and homocysteinemia
    Weitere Verfasser: “...Qiu, Wen-juan...”
    Aufsatz

  18. 18
    Molecular genetic analysis of 10 Chinese patients with glycogen storage disease type III
    Weitere Verfasser: “...Qiu, Wen-juan...”
    Aufsatz

  19. 19
    Clinical and mutational study of a Chinese infant with isovaleric acidemia
    Aufsatz

  20. 20
    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

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