MENU
Home
Add Document
Sign In
Create An Account
PDF Reader
Full Text
PostScript Table 1
Publication rates of abstracts presented at the Association of British Neurologists by category of abstract
Variable
Category
Proportion (%) published
OR (95% CI)
Type of presentation
Platform Poster Single centre Collaborative Case report Other studies
135/299 109/328 126/390 122/239 32/106 212/489
1.654 (1.97 to 2.286) p=0.002 0.457 (0.329 to 0.637) p
Suggest Documents
Novel EXOSC3 mutation causes complicated hereditary spastic paraplegia.
A recurrent mutation in KCNA2 as a novel cause of hereditary spastic paraplegia and ataxia.
Novel splice site mutation of SPG4 in a Chinese family with hereditary spastic paraplegia.
SPG20 mutation in three siblings with familial hereditary spastic paraplegia.
De novo REEP2 missense mutation in pure hereditary spastic paraplegia.
Hereditary spastic paraplegia due to a novel mutation of the REEP1 gene: Case report and literature review.
[Intrathecal baclofen therapy for hereditary spastic paraplegia].
A quantitative study of sensory function in hereditary spastic paraplegia.
SPG11 mutation in a Turkish familial hypobetalipoproteinemia family with hereditary spastic paraplegia.
Mutation analysis of SPAST, ATL1, and REEP1 in Korean Patients with Hereditary Spastic Paraplegia.
Gait evolution in a family with hereditary spastic paraplegia.
Dalfampridine in hereditary spastic paraplegia: a prospective, open study.
PMCA4 (ATP2B4) mutation in familial spastic paraplegia.
Targeted high throughput sequencing in hereditary ataxia and spastic paraplegia.
Lysosomal abnormalities in hereditary spastic paraplegia types SPG15 and SPG11.
A novel mutation in KIF5A in a Malian family with spastic paraplegia and sensory loss.
[Molecular genetics and gene analysis of hereditary spastic paraplegia].
Spastin mutation screening in Chinese patients with pure hereditary spastic paraplegia.
Genetic and phenotypic characterization of complex hereditary spastic paraplegia.
Mosaic dominant TUBB4A mutation in an inbred family with complicated hereditary spastic paraplegia.
Hereditary spastic paraplegia type 11 with a very late onset.
Hereditary spastic paraplegia: clinical principles and genetic advances.
Hereditary spastic paraplegia: clinical-genetic characteristics and evolving molecular mechanisms.
Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia.
Hereditary spastic paraplegia: a novel mutation and expansion of the phenotype variability in SPG10.
Hereditary spastic paraplegia: a novel mutation and expansion of the phenotype variability in SPG10. - PDF Download Free
654KB Sizes
0 Downloads
10 Views
Download PDF
Recommend Documents
Novel EXOSC3 mutation causes complicated hereditary spastic paraplegia.
A recurrent mutation in KCNA2 as a novel cause of hereditary spastic paraplegia and ataxia.
Novel splice site mutation of SPG4 in a Chinese family with hereditary spastic paraplegia.
SPG20 mutation in three siblings with familial hereditary spastic paraplegia.
De novo REEP2 missense mutation in pure hereditary spastic paraplegia.
Hereditary spastic paraplegia due to a novel mutation of the REEP1 gene: Case report and literature review.
[Intrathecal baclofen therapy for hereditary spastic paraplegia].
A quantitative study of sensory function in hereditary spastic paraplegia.
SPG11 mutation in a Turkish familial hypobetalipoproteinemia family with hereditary spastic paraplegia.
Mutation analysis of SPAST, ATL1, and REEP1 in Korean Patients with Hereditary Spastic Paraplegia.
×
Sign In
Login with Facebook
Don't have an account?
Forgot Password?
×
Sign Up
By clicking register, I agree to your terms