遗传性痉挛性截瘫

Troyer综合征回访：复杂遗传性痉挛性截瘫的临床和放射学研究

Troyer syndrome revisited : A clinical and radiological study of a complicated hereditary spastic paraplegia

遗传性痉挛性截瘫家系的基因定位与突变检测

Gene Mapping and Mutation Detection in Families with Hereditary Spastic Paraplegia

目的探讨遗传性痉挛性截瘫伴薄型胼胝体（HSPTCC）的临床特征。

Objective To explore the clinical characteristics of hereditary spastic paraplegia with thin corpus callosum ( HSP TCC ) .

目的：分析遗传性痉挛性截瘫伴胼胝体发育不良（HSP-TCC）的临床特点，以提高对此病的认识。

Aim : To explore the feature of hereditary spastic paraplegia with thin corpus callosum ( HSP-TCC ) for the profound recognition of this disease .

遗传性痉挛性截瘫散发病例的诊断

Hereditary spastic paralegia : Diagnosis and analysis of 24 sporadic cases

遗传性痉挛性截瘫一大家系19例遗传学分析

Genetic analysis for 19 cases of hereditary spastic paraplegia in a family

遗传性痉挛性截瘫伴薄型胼胝体的临床特征

Clinical characteristics of hereditary spastic paraplegia with thin corpus callosum

结论遗传性痉挛性截瘫散发病例的临床特点与有家族史者相似。

Conclusions The clinical characteristics in HSP cases are similar to familial history .

伴胼胝体发育不良和癫痫的遗传性痉挛性截瘫的一个新基因位点

A novel locus for hereditary spastic paraplegia with thin corpus callosum and epilepsy

遗传性痉挛性截瘫3例报告

A report 3 of cases with hereditary spastic paraplegia

五例遗传性痉挛性截瘫

Hereditary Spastic Paraplegia of 5 Cases

遗传性痉挛性截瘫的一种复杂表现形式：西尔弗综合征的临床、遗传学和候选基因研究

A clinical , genetic and candidate gene study of Silver syndrome , a complicated form of hereditary spastic paraplegia

一个患有瘫痪症的病人。遗传性痉挛性截瘫患者致病基因突变特征及其与临床表型的关系

Characteristics of Mutation of Disease-causing Genes in Chinese Patients Diagnosed as Hereditary Spastic Paraplegia and Its Relation to Clinical Phenotype

杜克研究中心的科学家们研究了两个存在遗传性痉挛性截瘫患者的家庭。

The Duke scientists began their search for genes associated with the disease by studying two families whose members had hereditary spastic paraplegia .