- Thinning of the Corpus Callosum and Cerebellar Atrophy is Correlated with Phenotypic Severity in a Family with Spastic Paraplegia Type 11
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Rajakulendran S, Paisan-Ruiz C, Houlden H
- KMID: 2178975
- J Clin Neurol.
- 2011 Jun;7(2):102-104.
- doi: 10.3988/jcn.2011.7.2.102
BACKGROUND: Mutations in the spatacsin gene are associated with spastic paraplegia type 11 (SPG11), which is the most-common cause of autosomal recessive hereditary spastic paraplegia. Although SPG11 has diverse phenotypes,... -
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- Automated Brainstem Segmentation Detects Differential Involvement in Atypical Parkinsonian Syndromes
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Bocchetta , Iglesias J, Chelban V, Jabbari E, Lamb R, Russell LL, Greaves CV, Neason M, Cash DM, Thomas DL, Warren JD, Woodside J, Houlden H, Morris HR, Rohrer JD
- KMID: 2501668
- J Mov Disord.
- 2020 Jan;13(1):39-46.
- doi: 10.14802/jmd.19030
Objective Brainstem segmentation has been useful in identifying potential imaging biomarkers for diagnosis and progression in atypical parkinsonian syndromes (APS). However, the majority of work has been performed using manual... -
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