Research for Herbal Preservation in Fruit and Vegetable Storage Disease 草本植物提取物在果蔬贮藏中的研究进展
Barrier dysfunction and pathogenesis of neutral lipid storage disease with ichthyosis ( Chanarin-Dorfman syndrome) 伴鱼鳞病的中性脂质贮存异常的发病机制和屏障功能障碍(Chanarin-Dorfman综合征)
Objective To develop and evaluate a simple, fast and accurate prenatal diagnosis method for glycogen storage disease Ia ( GSD Ia) in Chinese. 目的探讨中国人Ia型糖原累积病简便、快速、准确的产前诊断方法。
Objective To study renal involvement in hepatic glycogen storage disease ( GSD) in childhood. 目的观察儿童期肝糖原贮积症(GSD)的肾脏并发症。
Genotype/ phenotype correlation in glyco-gen storage disease type 1b: A multicentre study and review of the literature 1b型糖原贮积症中基因型和表现型间的相关性:一项多中心研究和文献回顾
Ultrastructural study on live tissue in a case of glycogen storage disease type ⅰ 糖原累积病Ⅰ型肝脏组织的超微结构观察
Lipid storage myopathy is one kind of autosomal recessive inherited disease with lipid abnormally sludging in the muscle cell. 脂质沉积性肌病是一种肌细胞内脂肪异常沉积引起的常染色体隐性遗传病。
Glycogen Storage Disease Associated with Lipid Storage Myopathy 糖原贮积症伴脂质贮积症
The effects of storage temperature on the post-harvested disease and physiological metabolize in muskmelon 贮藏温度对甜瓜果实采后病害和生理代谢的影响
Clinical and Mutation Analysis of Glycogen Storage Disease Type ⅲ 糖原累积症-Ⅲ型的临床和糖原脱枝酶基因突变分析
Mutation analysis of glycogen debrancher enzyme gene in five Chinese patients with glycogen storage disease type ⅲ 糖原贮积症Ⅲ型基因突变的初步研究
Clinical and genomic study of the infant with glycogen storage disease type ⅱ 糖原累积病Ⅱ型的临床分析和基因学检测
Recent advances of clinical and genomic study of glycogen storage disease type ⅲ 糖原累积病Ⅲ型临床和基因研究进展
The clinical and pathological features of Chinese patients of type ⅰ glycogen storage disease with renal involvement Ⅰ型糖原贮积症肾损害临床表现和病理改变
Neonatal type IV glycogen storage disease associated with null mutations in glycogen branching enzyme 1 糖原分枝酶1无效突变相关性IV型糖原贮积病新生儿亚型
Discussion on the lipid storage myopathy by the collateral disease theory 从络病论治脂质沉积性肌病
Prenatal diagnosis of glycogen storage disease Ia by screening for hot spot mutations in combination with the 1176 nucleotide polymorphism linkage analysis 葡萄糖6磷酸酶基因热点突变检测结合1176多态位点连锁分析快速产前诊断Ia型糖原累积病
Renal complications of hepatic glycogen storage disease 肝糖原贮积症肾脏并发症的临床观察
Advances in the Study of Glycogen Storage Disease Type ⅱ Ⅱ型糖原累积病的研究进展
Research Advances of Glycogen Storage Disease Type I 糖原累积病Ⅰ型研究的新进展
Molecular Genetics Analysis of Glycogen Storage Disease Ia in Chinese Family 糖原累积病Ⅰa型分子遗传学家系研究
Objective To obtain the mutation spectrum of glucose-6-phosphatase ( G6Pase) gene in Chinese patients with glycogen storage disease type ⅰ a ( GSD ⅰ a) and to analyze the relationship of its genotype and phenotype. 目的了解中国人葡萄糖6磷酸酶(G6Pase)基因突变谱和突变热点,并分析糖原累积病Ⅰa型(GSDⅠa)基因型和临床表型的相关性。
Benign course of glycogen storage disease type IIb in two brothers: Nature or nurture? 兄弟二人IIb型糖原贮积症的良性病程:自然还是营养的结果?
The effects of storage temperature on mango post-harvest disease and physiological metabolize were investigated. 采用不同温度贮藏芒果,研究了贮藏温度对采后病害及生理生化的影响。
Ethical Problems on Collection, Storage and Use of the Important Disease Genetic Resources 重大疾病遗传资源收集和保存、利用中的伦理学研究
Objective To investigate the molecular genetic mechanism of a patient with glycogen storage disease la. 目的研究1例糖原累积病Ⅰa型患者发病的分子遗传学机制。
The author will also analyze the unfavorable factors in developing potato industry through the analysis in market factors, storage factors, logistics factors, disease disaster detection factors,, marketing channels and marketing mode, and competitors. 通过对市场因素,储藏因素,物流因素,病灾害检测因素、意识,营销渠道和营销模式,竞争者等的分析得出定边县马铃薯产业的不利因素。
Therefore, physicians must have sufficient recognition for this disease, and be on the alert for hepatic glycogen storage disease, give a right and prompt diagnosis combined with family history, physical examinations and laboratory findings. 结论肝糖原累积病临床表现多样,要及时准确地诊断本病,需要对本病有充分的认识,结合患者的家族史、临床表现及各种实验室,影像学检查结果正确地加以综合分析。