Search Results - Mollaki, V.

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  1. 1
    Lysosomal acid lipase deficiency in Greece: A rare inborn error of metabolism presenting with dyslipidaimia and liver disease

    Lysosomal acid lipase deficiency in Greece: A rare inborn error of metabolism presenting with dyslipidaimia and liver disease by Drogari, E, Mollaki, V, Christomanou, H, Stamatelopoulos, K, Manolaki, N

    Published in Atherosclerosis
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  2. 2
    Homozygous familial hypercholesterolaemia in Greece: Epidemiological data from 29 patients

    Homozygous familial hypercholesterolaemia in Greece: Epidemiological data from 29 patients by Drogari, E, Mavroidis, N, Laios, E, Proyas, P, Mollaki, V

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  3. 3
    Pharmacogenetic profile of lipid response to atorvastatin in children and adolescents with familial Hypercholesterolemia

    Pharmacogenetic profile of lipid response to atorvastatin in children and adolescents with familial Hypercholesterolemia by Manolopoulos, V.G, Drogari, E, Ragia, G, Mollaki, V, Elens, L, Van Schaik, R.H.N

    Published in Clinical therapeutics
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  4. 4
    Polymorphisms and haplotypes in MyD88 are associated with the development of sarcoidosis: a candidate-gene association study

    Polymorphisms and haplotypes in MyD88 are associated with the development of sarcoidosis: a candidate-gene association study by Daniil, Z., Mollaki, V., Malli, F., Koutsokera, A., Antoniou, K. M., Rodopoulou, P., Gourgoulianis, K., Zintzaras, E., Vassilopoulos, G.

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  5. 5
    Homozygous familial hypercholesterolaemia in Greece: Epidemiology, phenotypic and genotypic characteristics from 39 patients

    Homozygous familial hypercholesterolaemia in Greece: Epidemiology, phenotypic and genotypic characteristics from 39 patients by Drogari, E., Laios, E., Progia, P., Mollaki, V.

    Published in Atherosclerosis
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  6. 6
    Lysosomal Acid Lipase Deficiency In Greece: Enzymatic And Molecular Analysis Of 33 Patients Using Dbs Screening

    Lysosomal Acid Lipase Deficiency In Greece: Enzymatic And Molecular Analysis Of 33 Patients Using Dbs Screening by Drogari, E., Hamilton, J., Mollaki, V., Sdoggou, T., Galina, P., Kamenets, E., Zakharova, E.

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  7. 7
    The FcγRIIa His131Arg polymorphism and its association with myocardial infarction

    The FcγRIIa His131Arg polymorphism and its association with myocardial infarction by Mollaki, V., Steeds, R. P., Samani, N. J., Channer, K. S., Daly, M. E.

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  8. 8
    The FcgammaRIIa His131Arg polymorphism and its association with myocardial infarction

    The FcgammaRIIa His131Arg polymorphism and its association with myocardial infarction by Mollaki, V, Steeds, R P, Samani, N J, Channer, K S, Daly, M E

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  9. 9
    MS52 HOMOZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA (FH) IN GREECE

    MS52 HOMOZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA (FH) IN GREECE by Drogari, E., Progias, P., Skouma, A., Elisaf, M., Mollaki, V.

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  10. 10
    Abstract: P1400 CHARACTERIZATION OF THE LOW DENSITY LIPOPROTEIN RECEPTOR GENE ( LDLR) MUTATIONS IN GREEK FAMILIES WITH FAMILIAL HYPERCHOLESTEROLEMIA (FH)

    Abstract: P1400 CHARACTERIZATION OF THE LOW DENSITY LIPOPROTEIN RECEPTOR GENE ( LDLR) MUTATIONS IN GREEK FAMILIES WITH FAMILIAL HYPERCHOLESTEROLEMIA (FH) by Mollaki, V, Mavroidis, N, Laios, E, Koniari, E, Nikola, A, Tsoutsou, E, Skouma, A, Drogari, E

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  11. 11
    P348 MOLECULAR DIAGNOSIS OF FAMILIAL HYPERCHOLESTEROLEMIA (FH) IN GREECE. KNOWN AND NOVEL MUTATIONS IN THE LOW DENSITY LIPOPROTEIN RECEPTOR ( LDLR) GENE

    P348 MOLECULAR DIAGNOSIS OF FAMILIAL HYPERCHOLESTEROLEMIA (FH) IN GREECE. KNOWN AND NOVEL MUTATIONS IN THE LOW DENSITY LIPOPROTEIN RECEPTOR ( LDLR) GENE by Mollaki, V., Progias, P., Skouma, A., Drogari, E.

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