Hníková 0.1, Delange F.2, Kračmar P.3, Vinohradská H.4, Bílek R.5 :
Experience in the Monitoring of Maternal and Neonatal
Iodine Supply in the Czech Republic
|
3 |
Fremuth J.‘, Sýkora J.‘, Boday A.2, Musil F.3, Varvařovská J.‘, :
Genetic Polymorphisms of UGT 1A1*28 in the TATA-box Promoter Region of Bilirubin Uridinediphosphate-glucuronosyltransferase Gene
in Children with Gilbert´s Syndrome
|
7 |
Rosipal Š., Kapellerová A.2, Tamášová M.1 :
Prognosis of Idiopathic Pulmonary Hemosiderosis at the Chud Age
|
14 |
Šimková J.‘, Ganevová M.2, Radvanská J.2, Čapková Š.‘ :
Vascular Anomalies in Children — a New Classification System, Natural History and Treatment
|
20 |
Al Kaissi A.1, Ghaehem M. B.‘, Chehida F. B.2, Kozlowski K.3 :
Sad Facies, Spinal Malsegmentation, Progressive Vicious
Kypboscoliosis, Multiple Wormian Bones, Basilar
Impression — A Novel Syndrome. Report of Two Sisters
|
28 |
Al Kaissi A.1, Ghachem M. B.1, Nassib N.1, Chehida F. B.2, Kozlowski K.3:
Unique Pattern Syndrome of Distinctive Facies, Short
Stature, Kyphoscoliosis, Craniosynostosis, Hyperlaxity and
Dyslexia
|
32 |
