Search Results - Gyürüs, P

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  1. 1
    Deletion patterns of dystrophin gene in Hungarian patients with Duchenne/Becker muscular dystrophies

    Deletion patterns of dystrophin gene in Hungarian patients with Duchenne/Becker muscular dystrophies by Herczegfalvi, Á, Tóth, G, Gyürüs, P, Morava, É, Endreffy, E, Fodor, F, Mechler, F, László, A, Raskó, I, Melegh, B

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  2. 2
    Distribution of Q188R and N314D mutations in the Hungarian galactosemic population

    Distribution of Q188R and N314D mutations in the Hungarian galactosemic population by Horváth, A., Gyurus, P., Kis, A., László, A., Schuler, Á., Kosztolányi, G., Melegh, B.

    Published in Human mutation
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  3. 3
    Trinucleotide repeat polymorphism at five disease loci in mixed Hungarian population

    Trinucleotide repeat polymorphism at five disease loci in mixed Hungarian population by Gyürüs, Péter, Molnár, János, Melegh, Béla, Tóth, Gábor, Morava, Éva, Kosztolányi, György, Méhes, Károly

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  4. 4
    Incidence trends for childhood type 1 diabetes in Europe during 1989–2003 and predicted new cases 2005–20: a multicentre prospective registration study

    Incidence trends for childhood type 1 diabetes in Europe during 1989–2003 and predicted new cases 2005–20: a multicentre prospective registration study by Patterson, Christopher C, Dr, Dahlquist, Gisela G, Prof, Gyürüs, Eva, MD, Green, Anders, Prof, Soltész, Gyula, Prof

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  5. 5
    Indirect genotype analysis as a diagnostic procedure in Marfan syndrome

    Indirect genotype analysis as a diagnostic procedure in Marfan syndrome by Laudahn, B M, Gyürüs, P, Orth, U, Gal, A, Nienaber, C A

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  6. 6
    Trends in childhood type 1 diabetes incidence in Europe during 1989–2008: evidence of non-uniformity over time in rates of increase

    Trends in childhood type 1 diabetes incidence in Europe during 1989–2008: evidence of non-uniformity over time in rates of increase by Patterson, C. C., Gyürüs, E., Rosenbauer, J., Cinek, O., Neu, A., Schober, E., Parslow, R. C., Joner, G., Svensson, J., Castell, C., Bingley, P. J., Schoenle, E., Jarosz-Chobot, P., Urbonaité, B., Rothe, U., Krzisnik, C., Ionescu-Tirgoviste, C., Weets, I., Kocova, M., Stipancic, G., Samardzic, M., de Beaufort, C. E., Green, A, Dahlquist, G. G., Soltész, G.

    Published in Diabetologia
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  7. 7
    Indirect genotype analysis as a diagnostic procedure in Marfan syndrome

    Indirect genotype analysis as a diagnostic procedure in Marfan syndrome by Laudahn, B M, Gyürüs, P, Orth, U, Gal, A, Nienaber, C A

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  8. 8
    Ancillary science with Ariel: feasibility and scientific potential of young stellar object observations

    Ancillary science with Ariel: feasibility and scientific potential of young stellar object observations by Gyürüs, B., Kiss, Cs, Morales, J.C., Nakhjiri, N., Marton, G., Ábrahám, P., Kóspál, Á., Moór, A., Szabó, Gy.M., Szabó, R.

    Published in Experimental astronomy
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