hereditary spastic paraplegia - Globe Thesis

Keyword [hereditary spastic paraplegia] Result: 1 - 20 \| Page: 1 of 3
1.	Gene Mapping And Mutation Detection In Families With Hereditary Spastic Paraplegia
2.	Characteristics Of Mutation Of Disease-causing Genes In Chinese Patients Diagnosed As Hereditary Spastic Paraplegia And Its Relation To Clinical Phenotype
3.	Clinical Features And Identification Of The Disease-Causing Genes In The Kindreds Of Hereditary Spastic Paraplegia And Charcot-Marie-Tooth Disease
4.	Clinical Features And Spastin Gene Mutation Analysis Of Patients With Hereditary Spastic Paraplegia
5.	Mutation Analysis Of The Candidate Genes Of A Novel Subtype Of Hereditary Spastic Paraplegia
6.	Mutation Analysis Of The Spastin Gene In Chinese Patients With Hereditary Spastic Paraplegia Disease
7.	The Research On Gene Mutation Analysis Of SPG4 And SPG3A In Hereditary Spastic Paraplegia Patients
8.	Gene Sequence Analysis Of Hereditary Spastic Paraplegia Pedigree PLP1
9.	Research On Clinical Features And Mitochondrial DNA Mutation Analysis Of Hereditary Spastic Paraplegia Type 4 (SPG4) Patients
10.	Clinical Features And Mutation Analysis Of The Spastin Gene In A Hereditary Spastic Paraplegia Family
11.	Features Of Magnetic Resonance Imaging In Hereditary Spastic Paraplegia Due To Spastin Mutation And Reep1 Mutation
12.	Investigation Of SLC33A1Gene Function And Its Role In Hereditary Spastic Paraplegia Using Zebrafish Model
13.	Mutation Analysis Of Infectious And Hereditary Diseases Using Next-generation Sequencing
14.	Clinicai And Genetic Analysis Of Patients With Kennedy’s Disease And Hereditary Spastic Paraplegia
15.	Exome Sequencing Identifies Novel Compound Heterozygous Mutations In SPG11That Cause Autosomal Recessive Hereditary Spastic Paraplegia
16.	Homozygous Embryos With Slc33a1Missense Mutation S113R Showed Early Developmental Arrest
17.	Genetic Analysis Of SPG4(SPAST)and SPG3A (ATL1) Genes In Hereditary Spastic Paraplegia Patients
18.	Hereditary Spastic Paraplegia With Thin Corpus Callosum In A Family Clinical Features And Gene Mutation Analysis
19.	Research On The Function And The Underlying Mechanism Of SPG42Causative Gene SLC33A1
20.	Features Of Brain MRI In Pure Hereditary Spastic Paraplegia Of SPG6Types
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