Charu Sharma,Hemanshi Shah,Mukta Waghmare et al.
Charu Sharma et al.
Type I intestinal atresias (webs) are rare causes of gastrointestinal obstruction in infants, the most common site being the second portion of the duodenum. According to the Louw and Barnard classification, type 1 atresia has been defined a...
A novel de novo 20q13.11q13.12 microdeletion in a boy with neurodevelopmental disorders - case report [0.03%]
神经发育障碍男孩的新发20q13.11q13.12微缺失案例报告
Joanna Bernaciak,Barbara Wiśniowiecka-Kowalnik,Jennifer Castañeda et al.
Joanna Bernaciak et al.
Copy-number variants (CNVs) are an important cause of human neurodevelopmental disorders. We present the first case of a 424 kb de novo 20q13.11q13.12 microdeletion in a patient with attention deficit disorder, tics and autistic behaviors, ...
A novel de novo 20q13.11q13.12 microdeletion in a boy with neurodevelopmental disorders - case report [0.03%]
一名患有神经发育障碍的男孩的新发20q13.11q13.12微缺失病例报告
Joanna Bernaciak,Barbara Wiśniowiecka-Kowalnik,Jennifer Castañeda et al.
Joanna Bernaciak et al.
Copy-number variants (CNVs) are an important cause of human neurodevelopmental disorders. We present the first case of a 424 kb de novo 20q13.11q13.12 microdeletion in a patient with attention deficit disorder, tics and autistic behaviors, ...
Barbara Kaczorowska-Hać,Jan Jacek Kaczor
Barbara Kaczorowska-Hać
Hereditary hemochromatosis type 1 is an autosomal recessive disorder caused by HFE gene mutations, which is an iron homeostasis metabolism controlling co-factor. Adults with male predomination present with clinical symptoms derived by iron ...
Barbara Kaczorowska-Hać,Jan Jacek Kaczor
Barbara Kaczorowska-Hać
Hereditary hemochromatosis type 1 is an autosomal recessive disorder caused by HFE gene mutations, which is an iron homeostasis metabolism controlling co-factor. Adults with male predomination present with clinical symptoms derived by iron ...
Anna Kłosowska,Agnieszka Ćwiklińska,Agnieszka Kuchta et al.
Anna Kłosowska et al.
Down syndrome (DS) is the most common chromosomal aberration and genetically determined cause of intellectual disability. DS patients often present with some congenital defects and chronic diseases, including early onset dementia, which aff...
Anna Kłosowska,Agnieszka Ćwiklińska,Agnieszka Kuchta et al.
Anna Kłosowska et al.
Down syndrome (DS) is the most common chromosomal aberration and genetically determined cause of intellectual disability. DS patients often present with some congenital defects and chronic diseases, including early onset dementia, which aff...
[Association of the meaning of life with satisfaction, the occurrence of subjective complaints and the family's economic status in the population of lower secondary school students] [0.03%]
生命意义感与初中生的幸福感、主观痛苦及家庭经济状况的关系调查研究
Dorota Zawadzka,Magdalena Stalmach,Anna Oblacińska et al.
Dorota Zawadzka et al.
Introduction: Feeling of meaning in life is extremely crucial factor of mental health. The lack of it can result in various disorders. Many authors, especially those connected with current of humanistic psychology underli...
[Association of the meaning of life with satisfaction, the occurrence of subjective complaints and the family's economic status in the population of lower secondary school students] [0.03%]
生命意义与中学生生活满意度、主观痛苦及家庭经济状况的关系研究
Dorota Zawadzka,Magdalena Stalmach,Anna Oblacińska et al.
Dorota Zawadzka et al.
Introduction: Feeling of meaning in life is extremely crucial factor of mental health. The lack of it can result in various disorders. Many authors, especially those connected with current of humanistic psychology underli...
[Can infrascanner be useful in hospital emergency departments for diagnosing minor head injury in children?] [0.03%]
颅脑 Injury在儿童中的诊断中近红外脑组织血氧代谢成像仪的作用如何？
Dorota Lewartowska-Nyga,Kamil Nyga,Grażyna Skotnicka-Klonowicz
Dorota Lewartowska-Nyga
Aim: The aim of the study was to determine whether Infrascanner screening is a test which would facilitate excluding acute intracranial bleeding in children after minor head injury and thus make it possible to limit indic...