1
|
Familial amyotrophic lateral sclerosis with frontotemporal dementia is linked to a locus on chromosome 9p13.2-21.3.
|
Brain
|
2006
|
5.36
|
2
|
Population based epidemiology of amyotrophic lateral sclerosis using capture-recapture methodology.
|
J Neurol Neurosurg Psychiatry
|
2011
|
2.08
|
3
|
Is the Frontal Assessment Battery reliable in ALS patients?
|
Amyotroph Lateral Scler Frontotemporal Degener
|
2012
|
2.06
|
4
|
Fasciculations and their F-response revisited: high-density surface EMG in ALS and benign fasciculations.
|
Clin Neurophysiol
|
2011
|
1.66
|
5
|
TDP-43 pathology in familial frontotemporal dementia and motor neuron disease without Progranulin mutations.
|
Brain
|
2007
|
1.55
|
6
|
Normal values for quantitative muscle ultrasonography in adults.
|
Muscle Nerve
|
2010
|
1.24
|
7
|
A frameshift mutation in LRSAM1 is responsible for a dominant hereditary polyneuropathy.
|
Hum Mol Genet
|
2011
|
1.18
|
8
|
Structural MRI reveals cortical thinning in amyotrophic lateral sclerosis.
|
J Neurol Neurosurg Psychiatry
|
2011
|
1.18
|
9
|
The ALS-FTD-Q: a new screening tool for behavioral disturbances in ALS.
|
Neurology
|
2012
|
0.92
|
10
|
Randomized sequential trial of valproic acid in amyotrophic lateral sclerosis.
|
Ann Neurol
|
2009
|
0.90
|
11
|
Quantitative muscle ultrasonography in amyotrophic lateral sclerosis.
|
Ultrasound Med Biol
|
2007
|
0.90
|
12
|
BSCL2 mutations in two Dutch families with overlapping Silver syndrome-distal hereditary motor neuropathy.
|
Neuromuscul Disord
|
2006
|
0.89
|
13
|
Muscle changes in amyotrophic lateral sclerosis: a longitudinal ultrasonography study.
|
Clin Neurophysiol
|
2011
|
0.89
|
14
|
Prevalence and distribution of fasciculations in healthy adults: Effect of age, caffeine consumption and exercise.
|
Amyotroph Lateral Scler
|
2010
|
0.87
|
15
|
H63D polymorphism in HFE is not associated with amyotrophic lateral sclerosis.
|
Neurobiol Aging
|
2012
|
0.87
|
16
|
Lithium lacks effect on survival in amyotrophic lateral sclerosis: a phase IIb randomised sequential trial.
|
J Neurol Neurosurg Psychiatry
|
2012
|
0.86
|
17
|
Early diagnosis of ALS: the search for signs of denervation in clinically normal muscles.
|
J Neurol Sci
|
2007
|
0.84
|
18
|
A case of neuromuscular mimicry.
|
Neuromuscul Disord
|
2006
|
0.83
|
19
|
Differentiation of hereditary spastic paraparesis from primary lateral sclerosis in sporadic adult-onset upper motor neuron syndromes.
|
Arch Neurol
|
2009
|
0.81
|
20
|
Rise and fall of skeletal muscle size over the entire life span.
|
J Am Geriatr Soc
|
2007
|
0.81
|
21
|
Increased plasma amyloid-beta42 protein in sporadic inclusion body myositis.
|
Acta Neuropathol
|
2009
|
0.80
|
22
|
CSF hypocretin-1 levels are normal in patients with amyotrophic lateral sclerosis.
|
Amyotroph Lateral Scler
|
2009
|
0.79
|
23
|
Diagnostic yield of muscle fibre conduction velocity in myopathies.
|
J Neurol Sci
|
2011
|
0.77
|
24
|
Seipin/BSCL2 mutation screening in sporadic adult-onset upper motor neuron syndromes.
|
J Neurol
|
2009
|
0.77
|
25
|
TDP-43 plasma levels are higher in amyotrophic lateral sclerosis.
|
Amyotroph Lateral Scler
|
2012
|
0.77
|
26
|
Intramuscular fibrous tissue determines muscle echo intensity in amyotrophic lateral sclerosis.
|
Muscle Nerve
|
2012
|
0.76
|
27
|
Transcranial direct current stimulation does not modulate motor cortex excitability in patients with amyotrophic lateral sclerosis.
|
Muscle Nerve
|
2011
|
0.76
|
28
|
TDP-43 plasma levels do not differentiate sporadic inclusion body myositis from other inflammatory myopathies.
|
Acta Neuropathol
|
2010
|
0.76
|
29
|
Acute deterioration of bulbar function after botulinum toxin treatment for sialorrhoea in amyotrophic lateral sclerosis.
|
Am J Phys Med Rehabil
|
2008
|
0.75
|
30
|
Letter: Recruitment of patients with both epilepsy and intellectual disability.
|
Epilepsia
|
2015
|
0.75
|
31
|
Parental age and the risk of amyotrophic lateral sclerosis.
|
Amyotroph Lateral Scler Frontotemporal Degener
|
2012
|
0.75
|
32
|
Cumulative effect of 5 daily sessions of θ burst stimulation on corticospinal excitability in amyotrophic lateral sclerosis.
|
Muscle Nerve
|
2013
|
0.75
|
33
|
Neuromuscular transmission in SCA6.
|
Ann Neurol
|
2004
|
0.75
|