Published in Vaccine on September 01, 1985
Long-term immunogenicity and efficacy of a reduced dose of plasma-based hepatitis B vaccine in young adults. Bull World Health Organ (1995) 1.45
Red cell alloantibodies in patients with thalassemia. Vox Sang (1990) 2.29
Chromosome studies in couples with repeated spontaneous abortions. Obstet Gynecol (1976) 1.66
The triplicated alpha-globin gene locus in beta-thalassaemia heterozygotes: clinical, haematological, biosynthetic and molecular studies. Br J Haematol (1996) 1.50
Efficacy and tolerability of formoterol Turbuhaler in children. Int J Clin Pract (2003) 1.43
Trisomy 3 mosaicism in a live-born infant. Clin Genet (1981) 1.39
Tissue oxygenation in patients with hemoglobinopathy H. Pediatr Hematol Oncol (1997) 1.38
Immunogenic effect of inactivated hepatitis B vaccine: comparison of 20 microgram and 40 microgram doses. J Med Virol (1981) 1.36
Skin hypersensitivity and in vitro lymphocytic reactivity to tuberculin in childhood. J Pediatr (1968) 1.19
Lazy-leukocyte syndrome. A case report. J Pediatr (1975) 1.10
Diabetes following mumps in sibs. Arch Dis Child (1971) 1.09
Effect of prolonged illumination (phototherapy) on concentrations of luteinizing hormone in human infants. Science (1978) 1.08
The heterogeneity of normal Hb A2-beta thalassaemia in Greece. Br J Haematol (1979) 1.05
A comparison of the homozygous states for G gamma and G gamma A gamma delta beta thalassaemia. Br J Haematol (1979) 1.04
Effectiveness of one tube osmotic fragility screening in detecting beta-thalassaemia trait. J Med Genet (1981) 1.03
A nursery outbreak of Serratia marcescens infection. Evidence of a single source of contamination. Am J Dis Child (1981) 1.03
Low mitotic activity of peripheral lymphocytes during the first two years of life. Arch Dis Child (1967) 1.02
Two novel polyadenylation mutations leading to beta(+)-thalassemia. Br J Haematol (1990) 1.01
Tumours of the head and neck in children. A clinico-pathological analysis of 1,007 cases. J Craniomaxillofac Surg (1988) 1.01
Quantification of liver iron overload by T2 quantitative magnetic resonance imaging in thalassemia: impact of chronic hepatitis C on measurements. J Pediatr Hematol Oncol (1999) 1.00
Rectal-axillary temperature difference in febrile and afebrile infants and children. Clin Pediatr (Phila) (1993) 0.99
Porencephalic cysts after amniocentesis. Arch Dis Child (1980) 0.99
Concordance of a point mutation 5' to the A gamma-globin gene with A gamma beta + hereditary persistence of fetal hemoglobin in Greeks. Blood (1986) 0.99
Prevalence of beta0 and beta+ thalassemia genes in Greek children with homozygous beta-thalassemia. Hemoglobin (1978) 0.98
Duplication of alpha-thalassaemia gene in three Greek families with haemoglobin H disease. Lancet (1970) 0.98
Occurrence of G gamma Hb F in Greek HPFH: analysis of heterozygotes and compound heterozygotes with beta thalassaemia. Br J Haematol (1979) 0.96
Growth of children with thalassaemia: effect of different transfusion regimens. Arch Dis Child (1970) 0.96
Mucoepidermoid carcinoma of the bronchus. Pediatr Hematol Oncol (2000) 0.95
The genetical interpretation of haemoglobin H disease. Hum Hered (1970) 0.94
Exchange transfusion in severe neonatal infection with sclerema. Arch Dis Child (1975) 0.93
Analysis of low density lipoprotein receptor gene mutations and microsatellite haplotypes in Greek FH heterozygous children: six independent ancestors account for 60% of probands. Hum Genet (1998) 0.93
Phagocytosis and killing ability of Candida albicans by blood leucocytes of healthy term and preterm babies. Arch Dis Child (1975) 0.92
1342C mutation in Gaucher's disease. Lancet (1995) 0.92
Serum alkaline phosphatase in infants with obstructive jaundice: relation to vitamin D supplementation. J Pediatr (1973) 0.92
Non-invasive myocardial iron assessment in thalassaemic patients. T2 relaxometry and magnetization transfer ratio measurements. Acta Radiol (2000) 0.92
Characterization of more than 85% of cystic fibrosis alleles in the Greek population, including five novel mutations. Hum Genet (1997) 0.92
Difficulty in swallowing, with aspiration pneumonia in infancy. Arch Dis Child (1967) 0.91
Raised IgA in idiopathic pulmonary haemosiderosis. Arch Dis Child (1975) 0.91
Low urinary glucose concentration: a reliable index of urinary tract infection. J Pediatr (1971) 0.90
Mild cystic fibrosis phenotype in patients with the 3272-26A > G mutation. J Med Genet (1995) 0.90
Growth and management of short stature in thalassaemia major. J Pediatr Endocrinol Metab (1998) 0.89
Corticosteroid treatment of erythema multiforme major (Stevens-Johnson syndrome) in children. Eur J Pediatr (1997) 0.89
Globin gene mapping in normal Hb A2 types of beta-thalassaemia. Br J Haematol (1982) 0.89
Generalized seborrhoeic dermatitis. Clinical and therapeutic data of 25 patients. Arch Dis Child (1975) 0.89
Idiopathic pulmonary haemosiderosis in children. Arch Dis Child (1968) 0.89
The response of leukocytes in the peripheral blood during and following exchange transfusion in the newborn. Pediatrics (1973) 0.89
Defective growth hormone secretion in primary microcephaly. J Pediatr (1974) 0.89
Steroids in treatment of pertussis. A controlled clinical trial. Arch Dis Child (1973) 0.88
Iron deficiency in Greece. Epidemiologic and hematologic studies. J Pediatr (1974) 0.88
Brucellosis in two thalassaemic patients infected by blood transfusions from the same donor. Acta Haematol (1976) 0.88
Erythroid marrow activity and hemoglobin H levels in hemoglobin H disease. J Pediatr Hematol Oncol (1998) 0.88
Glucose-6-phosphate Dehydrogenase Activity Levels in Enzyme-deficient Greek Individuals. Br Med J (1963) 0.88
A base substitution (T-->C) in codon 29 of the alpha 2-globin gene causes alpha thalassaemia. Br J Haematol (1993) 0.88
High mebendazole doses in pulmonary and hepatic hydatid disease. Arch Dis Child (1991) 0.88
Prenatal diagnosis of the thalassaemia syndromes by rapid DNA analytical methods. Mol Hum Reprod (1997) 0.87
Phenotypic and molecular diversity of haemoglobin H disease: a Greek experience. Br J Haematol (2000) 0.87
Molecular studies of beta-thalassemia heterozygotes with raised Hb F levels. Hemoglobin (2000) 0.87
The effects of television viewing in Greece, and the role of the paediatrician: a familiar triangle revisited. Eur J Pediatr (1996) 0.87
Prevalence of Au-Ag and Au-Ab in transfused children with thalassaemia in Greece. Arch Dis Child (1974) 0.87
A novel deletion in the beta-globin gene complex. Ann N Y Acad Sci (1985) 0.87
The clinical phenotype of beta and delta beta thalassemias in Greece. Eur J Pediatr (1982) 0.86
Immunological profile after splenectomy in children with beta-thalassaemia major. Acta Haematol (1987) 0.86
Genetic and molecular diversity in nondeletion Hb H disease. Proc Natl Acad Sci U S A (1981) 0.86
Flow-cytometric analysis of reticulocytes in normal cord blood. Acta Haematol (1993) 0.86
Experience of splenectomy and cholecystectomy in children with chronic haemolytic anaemia. J Pediatr Surg (1989) 0.85
Hydatid disease in Greek children. Am J Trop Med Hyg (1983) 0.85
Gentamicin in the treatment of purulent meningitis in neonates and infants. Acta Paediatr Scand (1973) 0.85
Social factors and professional attitudes as determinants of the frequency of small surgical procedures among children in Greece. Soz Praventivmed (1986) 0.84
Antibody dependent cytotoxicity of human colostrum phagocytes. Pediatr Res (1982) 0.84
Uncommon manifestations of histiocytosis X. Int J Oral Maxillofac Surg (1987) 0.84
Serum iron and unsaturated iron-binding capacity in the -thalassaemia trait: their relation to the levels of haemoglobins A, A 2 , and F. J Med Genet (1972) 0.83
Urinary vanillyl-mandelic acid (VMA) excretion by chronically anaemic children. Arch Dis Child (1968) 0.83
Assessment of liver iron overload by T2-quantitative magnetic resonance imaging: correlation of T2-QMRI measurements with serum ferritin concentration and histologic grading of siderosis. Magn Reson Imaging (1995) 0.83
When should at-risk patients with thalassaemia be boosted with hepatitis B vaccine? Lancet (1987) 0.82
Gaucher disease: four families with previously undescribed mutations. Proc Assoc Am Physicians (1996) 0.82
The silent serum cholinesterase gene. Acta Genet Stat Med (1967) 0.82
The impact of neocyte transfusion in the management of thalassaemia. Vox Sang (1996) 0.82
Molecular epidemiology of vertical human immunodeficiency virus type 1 transmission in Greece: evidence of non-B subtypes. J Hum Virol (2000) 0.82
A familial X/Y translocation in a boy with ichthyosis, hypogonadism and mental retardation. Clin Genet (1983) 0.82
Nutritional survey in Greek children: nutrient intake. Eur J Clin Nutr (1997) 0.82
Beta-thalassaemia, G-6-PD deficiency, and atypical cholinesterase in Cyprus. Br Med J (1972) 0.81
The interaction of alpha zero thalassaemia with Hb Icaria: three unusual cases of haemoglobinopathy H. Br J Haematol (1996) 0.81
Mutation analysis of ten exons of the CFTR gene in Greek cystic fibrosis patients: characterization of 74.5% of CF alleles including one novel mutation. Hum Genet (1995) 0.81
Serum levels of retinol, retinol-binding protein, carotenoids and triglycerides in children with beta-thalassemia major. Acta Haematol (1979) 0.81
Haplotype and mutation analysis in Greek patients with Wilson disease. Eur J Hum Genet (1999) 0.81
Cerebrospinal fluid and serum lysozyme activity in bacterial and viral meningitis. Helv Paediatr Acta (1977) 0.81
Metabolism of aromatic amino acids in collagen diseases: urinary excretion of 3-methoxy-4-hydroxymandelic acid and the interference of 3-methoxy-4-hydroxyphenylpyruvate. Clin Chim Acta (1967) 0.81
The clinical and haematological findings in children inheriting two types of thalassaemia: high-A2, type beta-thalassaemia, and high-F type or delta beta-thalassaemia. Br J Haematol (1973) 0.81
Different geographic origins of Hb Constant Spring [alpha(2) codon 142 TAA-->CAA]. Haematologica (2001) 0.81