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Česko-slovenská pediatrie
No.3, 26.2.2004

 
 
Pařízková E.1, Rozsíval P.1, Freiberger T.2, Komárek D.1:
X-linked Hypogammaglobulinaemia (Brutoiťs Disease) - Three Čase Studies and Molecular Genetic Studies in Their Families
119
Geier P.\ Šmakal O.2, Tichý T.3, Michálková K.4, Flogelová H.\ Skýpalová P.3:
Histological Findings in Children with Hydronephrosis
123
Kalousova J., Snajdauf J., Stýblová J., Fryč R., Pýcha K., Petrů O., Pachmannová D., Tomášek L.1:
Esophageal Atresia. Factors Influendng Outcome in Recent Era
128
Santavá A., Čapková P., Vrtěl R.:
Uniparental Paternal Disomia as a Cause of Angelman Syndrome in a Five-Year Girl
132
Bláhová K., Janda J.:
Acute Pyelonephritis in Childhood
136
Lisá L:
Importance of IGF-I
142
Špíšek R.1, Pončáková I.2, Petrů O.3, Šedivá A.1, Pohunek P.2, Vavřinec J.2:
Syndrome of Hyperimmunoglobulinemia E - Case Study and a Review of Literature
147
Olosová A.1, Chovancová D.2, Drobná H.2, Blažek B.3:
The Treatment with Heparin in Newborns and Children
152

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