Search Results - "Chaliasos, N"
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Cystic fibrosis-related eczematous dermatitis in an infant: another rare cause of hypereosinophilia
Published in Hippokratia (01-01-2018)Get full text
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Modulation of gut microbiota downregulates the development of food allergy in infancy
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
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
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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Effects of phosphodiesterase-5 inhibitor vardenafil on testicular androgen-binding protein secretion, the maintenance of foci of advanced spermatogenesis and the sperm fertilising capacity in azoospermic men
Published in Andrologia (01-05-2012)“…Summary We evaluated the effects of vardenafil on testicular androgen‐binding protein secretion (ABP). Bilaterally obstructed azoospermic (OA)‐men (n = 19)…”
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Recombinant human erythropoietin therapy in a transfusion-dependent β-thalassemia major patient
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
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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P-01-065 Effects of avanafil on semen quality and sperm cytoskeleton in oligoasthenospermic infertile men: a randomized controlled trial
Published in Journal of sexual medicine (01-05-2016)Get full text
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Bone minerals in β-thalassemia minor
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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A 7-month-old girl with fever and bleeding
Published in The Lancet (British edition) (20-04-1996)Get more information
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Effects of phosphodiesterase-5 inhibitor vardenafil on testicular androgen-binding protein secretion, the maintenance of foci of advanced spermatogenesis and the sperm fertilising capacity in azoospermic men: PDE5 inhibitors and Sertoli cell
Published in Andrologia (01-05-2012)Get full text
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Cytokine and adhesion molecule expression evolves between the neutrophilic and lymphocytic phases of viral meningitis
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
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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Red cell phosphate metabolism in full-term neonates
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
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…”
Get full text
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Bone mineral in β-thalassemia minor
Published in Bone (New York, NY) (1995)Get full text
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