International audienceSpinal muscular atrophy (SMA) type III and IV are autosomal recessive, slowly progressive lower motor neuron syndromes. Nevertheless, wider cerebral involvement has been consistently reported in mouse models. The objective of this study is the characterisation of spinal and cerebral pathology in adult forms of SMA using multimodal quantitative imaging.METHODS:Twenty-five type III and IV adult SMA patients and 25 age-matched healthy controls were enrolled in a spinal cord and brain imaging study. Structural measures of grey and white matter involvement and diffusion parameters of white matter integrity were evaluated at each cervical spinal level. Whole-brain and region-of-interest analyses were also conducted in the br...
BackgroundThe spectrum of motor neuron disease (MND) includes numerous phenotypes with various life ...
Spinal muscular atrophy (SMA) is a neurogenetic autosomal recessive disorder characterized by degene...
BackgroundThe spectrum of motor neuron disease (MND) includes numerous phenotypes with various life ...
International audienceSpinal muscular atrophy (SMA) type III and IV are autosomal recessive, slowly ...
This thesis examines the disease course and pathophysiology of motor dysfunction in spinal muscular ...
Objective: In this study we investigated the potential value of magnetic resonance imaging (MRI) and...
International audiencePurposeThe mechanisms underlying the topography of motor deficits in spinal mu...
Understanding the events that are responsible for a disease is mandatory for setting up a therapeuti...
Background: Traditionally, Multiple Sclerosis (MS) has been considered to be a predominantly white m...
Loss of the survival motor neuron gene (SMN1) is responsible for spinal muscular atrophy (SMA), the ...
Spinal muscular atrophy (SMA) is a neurogenetic autosomal recessive disorder characterized by degene...
BackgroundThe spectrum of motor neuron disease (MND) includes numerous phenotypes with various life ...
Spinal muscular atrophy (SMA) is a neurogenetic autosomal recessive disorder characterized by degene...
BackgroundThe spectrum of motor neuron disease (MND) includes numerous phenotypes with various life ...
International audienceSpinal muscular atrophy (SMA) type III and IV are autosomal recessive, slowly ...
This thesis examines the disease course and pathophysiology of motor dysfunction in spinal muscular ...
Objective: In this study we investigated the potential value of magnetic resonance imaging (MRI) and...
International audiencePurposeThe mechanisms underlying the topography of motor deficits in spinal mu...
Understanding the events that are responsible for a disease is mandatory for setting up a therapeuti...
Background: Traditionally, Multiple Sclerosis (MS) has been considered to be a predominantly white m...
Loss of the survival motor neuron gene (SMN1) is responsible for spinal muscular atrophy (SMA), the ...
Spinal muscular atrophy (SMA) is a neurogenetic autosomal recessive disorder characterized by degene...
BackgroundThe spectrum of motor neuron disease (MND) includes numerous phenotypes with various life ...
Spinal muscular atrophy (SMA) is a neurogenetic autosomal recessive disorder characterized by degene...
BackgroundThe spectrum of motor neuron disease (MND) includes numerous phenotypes with various life ...