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1.
Linkage Analysis of Microsatellite DNA Marker in Familial Simple Febrile Seizures;
家族性热性惊厥致病基因的遴选与筛查
2.
Mapping the Gene for BFIC Pedigrees;
良性家族性婴儿惊厥基因定位的研究
3.
Mutation Analysis of 5 Candidate Genes for One Chinese BFIC Family with a Novel Locus;
新的良性家族性婴儿惊厥候选基因的突变分析
4.
Studies on the Clinical Feature and Gene Diagnosis of Benign Familial Neonatal Convulsions;
良性家族性新生儿惊厥的临床及基因诊断研究
5.
The characters of clinic,electroencephalogram and gene in a Chinese family with benign familial infantile convulsions
良性家族性婴儿惊厥一家系的临床、脑电图及致病基因分析
6.
Mutation Analysis of 5 Candidate Genes for One Chinese BFIC Family with a Novel Locus (Ⅳ);
新的良性家族性婴儿惊厥候选基因的突变分析(Ⅳ)
7.
Clinical characteristics of ten pedigrees with generalized epilepsy with febrile seizures plus in China
中国10个全面性癫痫伴热性惊厥附加症家系的临床特征分析
8.
A Research on Prophylaxis of Febrile Convulsion and Brain Injuries with Topiramate, Valproate and Phenobarbital;
妥泰、丙戊酸钠、苯巴比妥预防热性惊厥及惊厥性脑损伤的实验研究
9.
Analysis of EEG in 316 patients with febrile convulsion
316例热性惊厥小儿的脑电图分析
10.
Analysis of EEG in 200 patients with febrile convulsion;
200例小儿热性惊厥的脑电图分析
11.
Analysis of Correlation Between Clinical Features and EEG Abnormality in Febrile Convulsion
热性惊厥临床与脑电图异常相关因素分析
12.
The Change and Meaning of Heme Oxygenase/Carbon Monoxide System in Children with Febrile Seizures;
热性惊厥患儿体内HO/CO水平变化及意义
13.
The Research Progress on Related Factors of Children′s Febrile Seizures
小儿热性惊厥发病相关因素的研究进展
14.
Changes of immunoresponsiveness and nursing care in children with recurrent febrile seizure
反复热性惊厥患儿免疫功能的改变及护理
15.
Study on Prophylaxis of Febrile Convulsion with Levetiracetam in Rats
左乙拉西坦预防动物热性惊厥的实验研究
16.
Clinical significance of changes of blood sodium,potassium,calcium and glucose in children with febrile convulsion
热性惊厥患儿血钠、钾、钙、糖变化的临床意义
17.
ANALYSIS OF ELECTROENCEPHALOGRAM ON 390 CHILDREN WITH FEBRILE CONVULSION
脑电图在儿童热性惊厥中的应用与分析
18.
Clinical Analysis and Gene Mutation Screening of Voltage-Gated Sodium Channel β1 Subunit in 2 Generalized Epilepsy with Febrile Seizures Plus Families
全面性癫伴热性惊厥附加症2家系临床分析及电压门控钠通道β1亚单位基因突变筛查