Czech-Slovak Pediatrics - Issue 1/2005
Original Papers
3
Experience in the Monitoring of Maternal and Neonatal Iodine Supply in the Czech Republic
O. Hníková, F. Delange, P. Kračmar, H. Vinohradská, R. Bílek
7
Genetic Polymorphisms of UGT 1A1*28 in the TATA-box Promoter Region of Bilirubin Uridinediphosphate-glucuronosyltransferase Gene in Children with Gilbert’s Syndrome
J. Fremuth, J. Sýkora, Á. Bóday, F. Musil, J. Varvařovská, F. Stožický, K. Kotaška, J. Schwarz, J. Skala
14
Prognosis of Idiopathic Pulmonary Hemosiderosis at the Child Age
Š. Rosipal, A. Kapellerová, M. Tamášová
Postgraduate Education
20
Vascular Anomalies in Children – a New Classification System, Natural History and Treatment
J. Šimková, M. Ganevová, J. Radvanská, Š. Čapková
Case Report
28
Sad Facies, Spinal Malsegmentation, Progressive Vicious Kyphoscoliosis, Multiple Wormian Bones, Basilar Impression – A Novel Syndrome. Report of Two Sisters
A. Al Kaissi, M. B. Ghachem, F. B. Chehida, K. Kozlowski
32
Unique Pattern Syndrome of Distinctive Facies, Short Stature, Kyphoscoliosis, Craniosynostosis, Hyperlaxity and Dyslexia
A. Al Kaissi, M. B. Ghachem, N. Nassib, F. B. Chehida, K. Kozlowski
Czech-Slovak Pediatrics
2005 Issue 1
Most read in this issue
- Sad Facies, Spinal Malsegmentation, Progressive Vicious Kyphoscoliosis, Multiple Wormian Bones, Basilar Impression – A Novel Syndrome. Report of Two Sisters
- Vascular Anomalies in Children – a New Classification System, Natural History and Treatment
- Genetic Polymorphisms of UGT 1A1*28 in the TATA-box Promoter Region of Bilirubin Uridinediphosphate-glucuronosyltransferase Gene in Children with Gilbert’s Syndrome
- Unique Pattern Syndrome of Distinctive Facies, Short Stature, Kyphoscoliosis, Craniosynostosis, Hyperlaxity and Dyslexia