Search Results - "Chaliasos, N"

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    Modulation of gut microbiota downregulates the development of food allergy in infancy by Tsabouri, S, Priftis, K N, Chaliasos, N, Siamopoulou, A

    Published in Allergologia et immunopathologia (01-01-2014)
    “…In humans, microbial colonisation of the intestine begins just after birth. However, development of the normal flora is a gradual process, which is initially…”
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    Impact of meteorological factors on the emergence of bronchiolitis in North-western Greece by Tsabouri, S, Gkoutsias, A, Lolis, C J, Makis, A, Chaliasos, N, Bartzokas, A

    Published in Allergologia et immunopathologia (01-01-2018)
    “…To evaluate the relationship between meteorological factors in North-western Greece and the incidence of bronchiolitis. Meteorological data (air temperature…”
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    Partial monosomy14q involving FOXG1 and NOVA1 in an infant with microcephaly, seizures and severe developmental delay by Fryssira, H, Tsoutsou, E, Psoni, S, Amenta, S, Liehr, T, Anastasakis, E, Skentou, Ch, Ntouflia, A, Papoulidis, I, Manolakos, E, Chaliasos, N

    Published in Molecular cytogenetics (02-08-2016)
    “…FOXG1 gene mutations have been associated with the congenital variant of Rett syndrome (RTT) since the initial description of two patients in 2008. The…”
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    Journal Article
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    Recombinant human erythropoietin therapy in a transfusion-dependent β-thalassemia major patient by MAKIS, A. C, CHALIASOS, N, HATZIMICHAEL, E. C, BOURANTAS, K. L

    Published in Annals of hematology (01-08-2001)
    “…We report on a 28-year-old patient with transfusion-dependent beta-thalassemia major, who was treated effectively with recombinant human erythropoietin…”
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    Vitamin D metabolites (25-hydroxyvitamin D, 24,25-dihydroxyvitamin D and 1,25-dihydroxyvitamin D) and osteocalcin in β-thalassaemia by Moulas, A, Challa, A, Chaliasos, N, Lapatsanis, PD

    Published in Acta Paediatrica (01-06-1997)
    “…Serum levels of the vitamin D metabolites 25‐hydroxyvitamin D, 24,25‐dihydroxyvitamin D, and 1,25‐dihydroxyvitamin D. and of osteocalcin. C‐tenninal…”
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    Bone minerals in β-thalassemia minor by Kalef-Ezra, J., Challa, A., Chaliasos, N., Hatzikonstantinou, I., Papaefstathiou, I., Cholevas, V., Glaros, D., Lapatsanis, P.

    Published in Bone (New York, N.Y.) (01-06-1995)
    “…Homozygous β-thalassemia is a severe hereditary disorder associated with osteopenia. Recently it was suggested that thalassemia minor may be a risk factor for…”
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    Cytokine and adhesion molecule expression evolves between the neutrophilic and lymphocytic phases of viral meningitis by Makis, Alexandros, Shipway, David, Hatzimichael, Eleftheria, Galanakis, Emmanouil, Pshezhetskiy, Dmitry, Chaliasos, Nikolaos, Stebbing, Justin, Siamopoulou, Antigone

    Published in Journal of interferon & cytokine research (01-09-2010)
    “…Viral meningitis is characterized by cerebrospinal fluid (CSF) lymphocyte pleocytosis, although neutrophils may predominate in the early phase. The T helper 1…”
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    Recombinant human erythropoietin therapy in a transfusion-dependent [beta]-thalassemia major patient by Makis, A, Chaliasos, N, Hatzimichael, E, Bourantas, K

    Published in Annals of hematology (01-08-2001)
    “…We report on a 28-year-old patient with transfusion-dependent β-thalassemia major, who was treated effectively with recombinant human erythropoietin (rHuEpo)…”
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    Journal Article
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    Red cell phosphate metabolism in full-term neonates by Challa, A, Chaliasos, N, Liossis, G, Palaskas, C, Staphylakis, C, Lapatsanis, P

    Published in Helvetica paediatrica acta (01-04-1985)
    “…The effects of hypoxia and feeding on red cell inorganic phosphate (Pi) concentrations were studied in neonates. Although hypoxia caused a rise in…”
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    Partial monosomy14q involving FOXG1 and NOVA1 in an infant with microcephaly, seizures and severe developmental delay by Fryssira, H, Tsoutsou, E, Psoni, S, Amenta, S, Liehr, T, Anastasakis, E, Skentou, Ch, Ntouflia, A, Papoulidis, I, Manolakos, E, Chaliasos, N

    Published in Molecular cytogenetics (01-01-2016)
    “…BACKGROUNDFOXG1 gene mutations have been associated with the congenital variant of Rett syndrome (RTT) since the initial description of two patients in 2008…”
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