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