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Acta Paediatrica (Oslo, Norway : 1992). Supplement|March 1, 1994
The screening programme for congenital hypothyroidism in Greece: evidence of iodine deficiency in some areas of the countryC Mengreli, L Yiannakou, S Pantelakis
Acta Paediatrica Scandinavica|May 1, 1976
The role of haemolysis in neonatal hyperbilirubinaemia as reflected in carboxyhaemoglobin levelsT F Necheles, U S Rai, T Valaes
European Journal of Pediatrics|November 1, 1995
Prolactin levels in febrile and afebrile seizuresP Sifianou, C Mengreli, G Makaronis, et al.
European Journal of Pediatrics|October 1, 1981
Neonatal screening for hypothyroidism in GreeceC Mengreli, K Kassiou, S Tsagaraki, et al.
Annales De Genetique|December 1, 1978
A cascade of chromosomal aberrations in three generations: a fragile 16q, an extra fragment and a rearranged 20G B Côté, S Papadakou-Lagoyanni, S Pantelakis
Biology of the Neonate|January 1, 1990
Alpha-fetoprotein in congenital hypothyroidismC Mengreli, E Sarafidou, S Petmezaki, et al.
Birth Defects Original Article Series|January 1, 1976
Experience with Sephadex gel filtration in assessing the risk of bilirubin encephalopathy in neonatal jaundiceT Valaes, J Kapitulnik, N A Kaufmann, et al.
Pediatric Research|August 1, 1980
Effectiveness and safety of prenatal phenobarbital for the prevention of neonatal jaundiceT Valaes, K Kipouros, S Petmezaki, et al.
Clinical Chemistry|August 1, 1979
Mechanized determination of the apparent unbound unconjugated bilirubin concentration in serumR P Wennberg, L F Rasmussen, C E Ahlfors, et al.
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