CFTR gene mutations - including three novel nucleotide substitutions - and haplotype background in patients with asthma, disseminated bronchiectasis and chronic obstructive pulmona... von TZETIS, Maria, EFTHYMIADOU, Alexandra, STROFALIS, Stefanos, PSYCHOU, Photini, DIMAKOU, Aikaterini, POULIOU, Eleni, DOUDOUNAKIS, Stavros, KANAVAKIS, Emmanuel

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Cat scratch disease in Greece von Karpathios, T, Golphinos, C, Psychou, P, Garoufi, A, Papadimitriou, A, Nicolaidou, P

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High mebendazole doses in pulmonary and hepatic hydatid disease von Messaritakis, J, Psychou, P, Nicolaidou, P, Karpathios, T, Syriopoulou, B, Fretzayas, A, Krikos, F, Matsaniotis, N

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Erythema nodosum in children: A prospective study von Kakourou, Talia, Drosatoua, Panayiota, Psychou, Fotini, Aroni, Kyriaki, Nicolaidou, Polyxeni

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Idiopathic Intracranial Hypertension in Children von Youroukos, Sotiris, Psychou, Fotini, Fryssiras, Spyros, Paikos, Petros, Nicolaidou, Polyxeni

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Endothelin‐1 in children with acute poststreptococcal glomerulonephritis and hypertension von NICOLAIDOU, POLYXENI, GEORGOULI, HELEN, MATSINOS, YIANNIS, PSYCHOU, FOTINI, MESSARITAKI, ANNA, GOURGIOTIS, DIMITRIS, ZEIS, PETROS

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Urinary excretion of endothelin-1 in children with absorptive idiopathic hypercalciuria von NICOLAIDOU, Polyxeni, GEORGOULI, Helen, GETSI, Vasiliki, TSAPRA, Helen, PSYCHOU, Fotini, MATSINOS, Yiannis G, ZEIS, Petros M, GOURGIOTIS, Dimitris

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Congenital Tuberculosis: A Case Report von Nicolaidou, Polyxeni, Psychou, Fotini, Stefanaki, Kalliopi, Tsitsika, Artemis, Syriopoulou, Vassiliki

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HODGKIN'S DISEASE IN A CHILD WITH SICKLE CELL DISEASE TREATED WITH HYDROXYUREA von Moschovi, Maria, Psychou, Fotini, Menegas, Damianos, Tsangaris, George Th, Tzortzatou-Stathopoulou, Fotini, Nikolaidou, Polyxeni

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Hydroxyurea and Hodgkin's Disease in A Child with Sickle Cell Anemia von Moschovi, M, Psychou, F, Menegas, D, Nikolaidou, P, Tzortzatou-Stathopoulou, F

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