glycogen disease
glycogen disease是什么意思、glycogen disease怎么读
读音：[英]
[ˈglaɪkədʒɪn dɪˈziːz]
glycogen disease 基本解释
网络 又叫糖原病; 糖原病
重点词汇
glycogen disease 双语例句
- 1、
Glycogen Synthase Kinase-3 β in Formation and Treatment of Parkinson's Disease
糖原合酶激酶-3β与帕金森病的发生及治疗 - 2、
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。 - 3、
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。 - 4、
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 - 5、
Glycogen Storage Disease Associated with Lipid Storage Myopathy
糖原贮积症伴脂质贮积症 - 6、
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 - 7、
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 - 8、
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 - 9、
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 - 10、
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 - 11、
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 - 12、
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 - 13、
Renal complications of hepatic glycogen storage disease
肝糖原贮积症肾脏并发症的临床观察 - 14、
Advances in the Study of Glycogen Storage Disease Type ⅱ
Ⅱ型糖原累积病的研究进展 - 15、
Research Advances of Glycogen Storage Disease Type I
糖原累积病Ⅰ型研究的新进展 - 16、
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 - 17、
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。 - 18、
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？ - 19、
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。 - 20、
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。