… Continuous variables were compared using Student t test or the Mann-Whitney U test as
appropriate. Categorical variables were compared using the chi-square test. The statistical …

Aim Galactosemia is a carbohydrate metabolism disorder with autosomal recessive
inheritance. The most frequent enzyme deficiency is galactose-1-phosphate-uridylytransferase, …

… TM system (Boehringer Mannheim), in order to minimise PCR-generated mutations, and
this was confirmed by sequencing of all the products following subcloning into the pGEM-T …

We report here the cloning, characterisation and developmental expression profile of the
Xenopus laevis CCAAT-enhancer binding protein β (xC/EBPβ) gene. The protein synthesised …

Introduction: The aim of this study was evaluation of broncoscopic findings in children with
congenital heart disease(CHD). Method: Bronchoscopy was performed in 37 patients with …

Aim: We aimed to evaluate the features and underlying diseases of the patients9 who diagnosed
laryngomalacia. Material-Method: We evaluated 50 patients with laryngomalacia who …

Introduction: Subglottic stenosis (SGS) is a congenital or acquired condition characterized
by a narrowing of the upper airway extending from just below the vocal folds to the lower …

… cm −1 which corresponds to the M o -O and M t -O vibrations, respectively. M o indicates
the metal ion at the octahedral site and M t indicates the metal ion at the tetrahedral site [25]. …

Methylphenidate is commonly believed to lower seizure threshold. The safe use of methylphenidate
has not been clarified in patients with attention-deficit hyperactivity disorder (ADHD) …

… The bulk Co3O4 exhibits antiferromagnetic transition temperature at T N = 33 K [1, 14] and …
KV = kBT to this case, the particle size near T t ∼ 31 K could be estimated as about 2.015 nm, …