Gray and white matter alterations in hereditary spastic paraplegia type SPG4 and clinical correlations

Accurate automatic estimation of total intracranial volume: A nuisance variable with less nuisance

(2015) Ian B. Malone et al.   NEUROIMAGE

Multimodal MRI-Based Study in Patients with SPG4 Mutations

(2015) Thiago J. R. Rezende et al.   PLoS One

Mutations in the SPG7 gene cause chronic progressive external ophthalmoplegia through disordered mitochondrial DNA maintenance

(2014) Gerald Pfeffer et al.   BRAIN

The Global Epidemiology of Hereditary Ataxia and Spastic Paraplegia: A Systematic Review of Prevalence Studies

(2014) Luis Ruano et al.   NEUROEPIDEMIOLOGY

Exome Sequencing Links Corticospinal Motor Neuron Disease to Common Neurodegenerative Disorders

(2014) G. Novarino et al.   SCIENCE

Diffusion tensor imaging inSPG11- andSPG4-linked hereditary spastic paraplegia

(2013) Francesco Garaci et al.   INTERNATIONAL JOURNAL OF NEUROSCIENCE

Klinik und Genetik der spastischen Spinalparalysen

(2013) L. Schöls et al.   Medizinische Genetik

Electrophysiological characterisation of motor and sensory tracts in patients with hereditary spastic paraplegia (HSP)

(2013) Kathrin N Karle et al.   Orphanet Journal of Rare Diseases

Cellular Pathways of Hereditary Spastic Paraplegia

(2012) Craig Blackstone   Annual Review of Neuroscience

Genetics of Hereditary Spastic Paraplegias

(2012) Rebecca Schüle et al.   SEMINARS IN NEUROLOGY

Delayed axonal degeneration in slow Wallerian degeneration mutant mice detected using diffusion tensor imaging

(2011) M. Xie et al.   NEUROSCIENCE

Mutation of FA2H underlies a complicated form of hereditary spastic paraplegia (SPG35)

(2010) Katherine J. Dick et al.   HUMAN MUTATION

Specific pattern of early white-matter changes in pure hereditary spastic paraplegia

(2010) Thomas Duning et al.   MOVEMENT DISORDERS

Unified segmentation based correction of R1 brain maps for RF transmit field inhomogeneities (UNICORT)

(2010) Nikolaus Weiskopf et al.   NEUROIMAGE

Correlation between pyramidal tract degeneration and widespread white matter involvement in amyotrophic lateral sclerosis: A study with tractography and diffusion-tensor imaging

(2009) Joe Senda et al.   Amyotrophic Lateral Sclerosis

Widespread thalamic and cerebellar degeneration in a patient with a complicated hereditary spastic paraplegia (HSP)

(2009) K. Seidel et al.   ANNALS OF ANATOMY-ANATOMISCHER ANZEIGER

Posterior fossa abnormalities in hereditary spastic paraparesis with spastin mutations

(2009) C Scuderi et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

Mutation analysis of the SPG4 gene in Italian patients with pure and complicated forms of spastic paraplegia

(2009) Angela Magariello et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

A probabilistic MR atlas of the human cerebellum

(2009) Jörn Diedrichsen et al.   NEUROIMAGE

Identification of the SPG15 Gene, Encoding Spastizin, as a Frequent Cause of Complicated Autosomal-Recessive Spastic Paraplegia, Including Kjellin Syndrome

(2008) Sylvain Hanein et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Axonal injury detected byin vivodiffusion tensor imaging correlates with neurological disability in a mouse model of multiple sclerosis

(2007) Matthew D. Budde et al.   NMR IN BIOMEDICINE