Search Results - Vinohradská, J.

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  1. 1
    WS09.4 Next generation sequencing in newborn screening for cystic fibrosis

    WS09.4 Next generation sequencing in newborn screening for cystic fibrosis by Vinohradská, J., Valaskova, I., Gaillyová, R.

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  2. 2
    P015 CFTR RealTime Panel using pre-plated LightSNiP assays is a good strategy for CFTR genotyping

    P015 CFTR RealTime Panel using pre-plated LightSNiP assays is a good strategy for CFTR genotyping by Vinohradská, J., Valášková, I., Gaillyová, R.

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  3. 3
    Expanding application of next generation sequencing in clinical laboratory

    Expanding application of next generation sequencing in clinical laboratory by Smetana, J., Wayhelova, M., Vallova, V., Zrnova, E., Synkova, I., Vaňásková, M., Vinohradská, J., Ošťádalová, E., Valášková, I., Kuglik, P.

    Published in Clinica chimica acta
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  4. 4
    P046 Cystic fibrosis newborn screening (CF NBS) in the Czech Republic: analysis of the false negative results

    P046 Cystic fibrosis newborn screening (CF NBS) in the Czech Republic: analysis of the false negative results by Holubová, A., Gaillyová, R., Skalická, V., Vinohradská, H., Hedelová, M., Libik, M., Valášková, I., Bartošová, J., Doušová, T., Holčíková, A., Homola, L., Votava, F., Macek, M.

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  5. 5
    WS10.6 Seven years of nationwide cystic fibrosis newborn screening in the Czech Republic: analysis of the IRT/DNA/IRT scheme outcomes

    WS10.6 Seven years of nationwide cystic fibrosis newborn screening in the Czech Republic: analysis of the IRT/DNA/IRT scheme outcomes by Holubová, A., Gaillyová, R., Skalická, V., Vinohradská, H., Dejmek, P., Libik, M., Valášková, I., Bartošová, J., Doušová, T., Holčíková, A., Homola, L., Kinclová, E., Votava, F., Macek, M.

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  6. 6
    7 Genetic prevention of cystic fibrosis as a part of the national strategy for rare diseases in University Hospital Brno, Czech Republic (genetic counselling – DNA analysis – newborn screening – education)

    7 Genetic prevention of cystic fibrosis as a part of the national strategy for rare diseases in University Hospital Brno, Czech Republic (genetic counselling – DNA analysis – newbo... by Gaillyová, R, Valášková, I, Nečasová, J, Spěšná, R, Vinohradská, H, Holčíková, A, Homolá, L, Pokojová, E, Dostál, O

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  7. 7
    8 Detection of the mutation D1152H in the CFTR gene in University Hospital Brno, Czech Republic

    8 Detection of the mutation D1152H in the CFTR gene in University Hospital Brno, Czech Republic by Gaillyová, R, Vaiásková, I, Kadlecová, J, HoiCíkova, A, Homola, L, Pokojová, E, Binková, I, Vinohradská, H

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  8. 8
    WS11.5 New approach for CF diagnosis based on chloride/potassium ion ratios analyzed in non-invasively obtained skin wipe sweat samples

    WS11.5 New approach for CF diagnosis based on chloride/potassium ion ratios analyzed in non-invasively obtained skin wipe sweat samples by Kuban, P, Durc, P, Foret, F, Pokojova, E, Skrickova, J, Homola, L, Dastych, M, Vinohradska, H

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  9. 9
    1037 Determination of Prealbumin, Selenium, Zinc and Iron Concentration in Serum for Monitoring the Nutrition Status of Phenylketonuric and Hyperphenylalaninemic Patients

    1037 Determination of Prealbumin, Selenium, Zinc and Iron Concentration in Serum for Monitoring the Nutrition Status of Phenylketonuric and Hyperphenylalaninemic Patients by Prochazkova, D, Kolbova, L, Jarkovsky, J, Vinohradska, H, Konecna, P, Dolezel, Z

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  10. 10
    PO-0136 Increased Risk Of Vitamin B12 Nutritional Deficiency In Long-term Treated Patients With Phenylketonuria And Hyperfenylalaninemia

    PO-0136 Increased Risk Of Vitamin B12 Nutritional Deficiency In Long-term Treated Patients With Phenylketonuria And Hyperfenylalaninemia by Prochazkova, D, Jarkovsky, J, Vinohradska, H, Benakova, H, Konecna, P, Machacova, L, Dolezel, Z

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  11. 11
    PO-0136Increased Risk Of Vitamin B12 Nutritional Deficiency In Long-term Treated Patients With Phenylketonuria And Hyperfenylalaninemia

    PO-0136Increased Risk Of Vitamin B12 Nutritional Deficiency In Long-term Treated Patients With Phenylketonuria And Hyperfenylalaninemia by Prochazkova, D, Jarkovsky, J, Vinohradska, H, Benakova, H, Konecna, P, Machacova, L, Dolezel, Z

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