Maja Drobnič Radobuljac,Yael Shmueli-Goetz
Maja Drobnič Radobuljac
Attachment is a behavioral and physiological system, which enables individual's dynamic adaptation to its environment. Attachment develops in close interaction between an infant and his/her mother, plays an important role in the development...
Childhood Osteoporosis and Presentation of Two Cases with Osteogenesis Imperfecta Type V [0.03%]
儿童低骨量及两例成骨不全V型报告
Nina Bratanic,Bojana Dzodan,Katarina Trebusak Podkrajsek et al.
Nina Bratanic et al.
Introduction: Osteogenesis imperfecta (OI) is etiologically heterogeneous disorder characterized by childhood osteoporosis. A subtype OI type V is caused by the same c.-14C>T mutation in the IFITM5 gene. Nevertheless, the...
Clinical, Genetic and Immunological Characteristics of Paediatric Autoimmune Polyglandular Syndrome Type 1 Patients in Slovenia [0.03%]
斯洛文尼亚儿童自身免疫性多腺体综合征1型患者的临床、遗传和免疫学特征
Nina Bratanic,Kai Kisand,Magdalena Avbelj Stefanija et al.
Nina Bratanic et al.
Introduction: Autoimmune polyglandular syndrome type 1 (APS-1) is an autosomal recessive disorder, caused by mutations in the AIRE gene. The major components of APS-1 are chronic mucocutaneous candidiasis (CMC), hypoparat...
Annual Psychological Screening in Youth and Young Adults with Type 1 Diabetes [0.03%]
1型糖尿病青少年人群中的年度心理筛查研究
Simona Klemenčič,Maartje de Wit,Miha Rutar et al.
Simona Klemenčič et al.
Aim: Youth and young adults with type 1 diabetes are at a great risk for developing depression and diabetes specific distress, therefore, systematic psychological screening is recommended. Routine psychological screening ...
Cytogenetic and Molecular Genetic Characterization of Children with Short Stature [0.03%]
儿童身材矮小的细胞遗传学和分子遗传学特征分析
Tinka Hovnik,Darja Šmigoc Schweiger,Primož Kotnik et al.
Tinka Hovnik et al.
Background: The deficiency of SHOX gene (short stature homeobox-containing gene) has been recognized as the most frequent monogenetic cause of short stature. SHOX gene has been associated with short stature in Turner synd...
Comparison of a Web-Based Dietary Assessment Tool with Software for the Evaluation of Dietary Records [0.03%]
基于网络的膳食评估工具与用于评价膳食记录软件的比较研究
Evgen Benedik,Barbara Koroušić Seljak,Maša Hribar et al.
Evgen Benedik et al.
Background: Dietary assessment in clinical practice is performed by means of computer support, either in the form of a web-based tool or software. The aim of the paper is to present the results of the comparison of a Slov...
Andraž Šmon,Urh Grošelj,Mojca Žerjav Tanšek et al.
Andraž Šmon et al.
Introduction: Newborn screening in whole Slovenia started in 1979 with screening for phenylketonuria (PKU). Congenital hypothyroidism (CH) was added into the programme in 1981. The aim of this study was to analyse the dat...
Tanja Pate,Miha Rutar,Tadej Battelino et al.
Tanja Pate et al.
Objectives: Type 1 diabetes is one of the most common chronic diseases in childhood. Active parental involvement, parental support in the diabetes management and family functioning are associated with optimal diabetes man...
Association of Average Telomere Length with Body-Mass Index and Vitamin D Status in Juvenile Population with Type 1 Diabetes [0.03%]
与1型糖尿病青少年患者体重指数和维生素D状态相关的平均端粒长度的关联研究
Tine Tesovnik,Jernej Kovac,Tinka Hovnik et al.
Tine Tesovnik et al.
Background: Type 1 diabetes (T1D) is an autoimmune chronic disease where hyperglycemia, increased risk of oxidative stress, advanced glycation end-products and other genetic and environmental factors lead to T1D complicat...
Clinical and Molecular Cytogenetic Characterisation of Children with Developmental Delay and Dysmorphic Features [0.03%]
发育迟缓和形态异常儿童的临床和分子细胞遗传学特征分析
Sara Bertok,Mojca Žerjav Tanšek,Primož Kotnik et al.
Sara Bertok et al.
Introduction: Developmental delay and dysmorphic features affect 1 - 3 % of paediatric population. In the last few years molecular cytogenetic high resolution techniques (comparative genomic hybridization arrays and singl...