OBJECTIVE: A recent neuroanatomical staging scheme of amyotrophic lateral sclerosis (ALS) indicates that a cortical lesion may spread, as a network disorder, both at the cortical level and via corticofugal tracts, including corticospinal projections providing direct monosynaptic input to α-motoneurons. These projections are involved preferentially and early in ALS. If these findings are clinically relevant, the pattern of paresis in ALS should primarily involve those muscle groups that receive the strongest direct corticomotoneuronal (CM) innervation. METHODS: In a large cohort (N=436), we analysed retrospectively the pattern of muscle paresis in patients with ALS using the UK Medical Research Council (MRC) scoring system; we subsequently c...
OBJECTIVE Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease of the motor system. T...
Abstract Background Split phenotypes, (split hand, elbow, leg, and foot), are probably unique to ALS...
Brainstem pathology is a pathognomonic feature of ALS encompassing lower cranial nerve and descendin...
Amyotrophic lateral sclerosis (ALS) represents the major adult-onset motor neuron disease. Both huma...
Introduction: Several studies have shown a significant amplitude decrement in compound muscle action...
Objective: This study aimed to investigate whether the spread pattern affects functional staging in ...
The development of amyotrophic lateral sclerosis (ALS) represents a singularly human, progressive ne...
Objective: Examine whether cortical thinning is a disease-specific phenomenon across the spectrum of...
Primary lateral sclerosis (PLS) is a slowly progressing disorder, which is characterized primarily b...
Amyotrophic lateral sclerosis is a fatal neurodegenerative disease characterized by progressive musc...
BACKGROUND Amyotrophic lateral sclerosis (ALS) is a primary progressive neurodegenerative disease...
Background: Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder clinically character...
This thesis examined patterns of disease in amyotrophic lateral sclerosis and explored novel methods...
Background: Amyotrophic lateral sclerosis (ALS) is a late-onset progressive neurodegenerative disord...
Objectives The neural activity of the primary motor cortex is variably synchronised with contralater...
OBJECTIVE Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease of the motor system. T...
Abstract Background Split phenotypes, (split hand, elbow, leg, and foot), are probably unique to ALS...
Brainstem pathology is a pathognomonic feature of ALS encompassing lower cranial nerve and descendin...
Amyotrophic lateral sclerosis (ALS) represents the major adult-onset motor neuron disease. Both huma...
Introduction: Several studies have shown a significant amplitude decrement in compound muscle action...
Objective: This study aimed to investigate whether the spread pattern affects functional staging in ...
The development of amyotrophic lateral sclerosis (ALS) represents a singularly human, progressive ne...
Objective: Examine whether cortical thinning is a disease-specific phenomenon across the spectrum of...
Primary lateral sclerosis (PLS) is a slowly progressing disorder, which is characterized primarily b...
Amyotrophic lateral sclerosis is a fatal neurodegenerative disease characterized by progressive musc...
BACKGROUND Amyotrophic lateral sclerosis (ALS) is a primary progressive neurodegenerative disease...
Background: Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder clinically character...
This thesis examined patterns of disease in amyotrophic lateral sclerosis and explored novel methods...
Background: Amyotrophic lateral sclerosis (ALS) is a late-onset progressive neurodegenerative disord...
Objectives The neural activity of the primary motor cortex is variably synchronised with contralater...
OBJECTIVE Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease of the motor system. T...
Abstract Background Split phenotypes, (split hand, elbow, leg, and foot), are probably unique to ALS...
Brainstem pathology is a pathognomonic feature of ALS encompassing lower cranial nerve and descendin...