Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
1
|
Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis.
|
Nat Genet
|
2009
|
4.38
|
2
|
X-linked bulbospinal neuronopathy: Kennedy disease.
|
Arch Neurol
|
2002
|
2.21
|
3
|
Are amygdalar volume alterations in children with Tourette syndrome due to ADHD comorbidity?
|
Dev Med Child Neurol
|
2008
|
2.11
|
4
|
Energy metabolism in amyotrophic lateral sclerosis.
|
Lancet Neurol
|
2010
|
2.00
|
5
|
Two German kindreds with familial amyotrophic lateral sclerosis due to TARDBP mutations.
|
Arch Neurol
|
2008
|
1.78
|
6
|
Four familial ALS pedigrees discordant for two SOD1 mutations: are all SOD1 mutations pathogenic?
|
J Neurol Neurosurg Psychiatry
|
2010
|
1.68
|
7
|
Global brain atrophy and corticospinal tract alterations in ALS, as investigated by voxel-based morphometry of 3-D MRI.
|
Amyotroph Lateral Scler Other Motor Neuron Disord
|
2005
|
1.55
|
8
|
Images in cardiovascular medicine. Cardiomyopathy in a Duchenne muscular dystrophy carrier and her diseased son: similar pattern revealed by cardiovascular MRI.
|
Circulation
|
2010
|
1.47
|
9
|
Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis.
|
Ann Neurol
|
2011
|
1.45
|
10
|
Heterozygous R1101K mutation of the DCTN1 gene in a family with ALS and FTD.
|
Ann Neurol
|
2005
|
1.42
|
11
|
Severity of depressive symptoms and quality of life in patients with amyotrophic lateral sclerosis.
|
Neurorehabil Neural Repair
|
2005
|
1.40
|
12
|
The chemokine CXCL13 is a prognostic marker in clinically isolated syndrome (CIS).
|
PLoS One
|
2010
|
1.32
|
13
|
Amyotrophic lateral sclerosis--a model of corticofugal axonal spread.
|
Nat Rev Neurol
|
2013
|
1.29
|
14
|
The chemokine CXCL13 in acute neuroborreliosis.
|
J Neurol Neurosurg Psychiatry
|
2009
|
1.26
|
15
|
IgG antibodies against measles, rubella, and varicella zoster virus predict conversion to multiple sclerosis in clinically isolated syndrome.
|
PLoS One
|
2009
|
1.25
|
16
|
Whole brain-based analysis of regional white matter tract alterations in rare motor neuron diseases by diffusion tensor imaging.
|
Hum Brain Mapp
|
2010
|
1.23
|
17
|
Riluzole in Huntington's disease: a 3-year, randomized controlled study.
|
Ann Neurol
|
2007
|
1.21
|
18
|
Disease severity and progression in progressive supranuclear palsy and multiple system atrophy: validation of the NNIPPS--Parkinson Plus Scale.
|
PLoS One
|
2011
|
1.15
|
19
|
Alternative trial design in amyotrophic lateral sclerosis saves time and patients.
|
Amyotroph Lateral Scler
|
2007
|
1.15
|
20
|
The modulation of Amyotrophic Lateral Sclerosis risk by ataxin-2 intermediate polyglutamine expansions is a specific effect.
|
Neurobiol Dis
|
2011
|
1.12
|
21
|
Neuroectodermally converted human mesenchymal stromal cells provide cytoprotective effects on neural stem cells and inhibit their glial differentiation.
|
Cytotherapy
|
2010
|
1.10
|
22
|
Accelerated aging phenotype in mice with conditional deficiency for mitochondrial superoxide dismutase in the connective tissue.
|
Aging Cell
|
2010
|
1.09
|
23
|
A randomized, double blind, placebo-controlled trial of pioglitazone in combination with riluzole in amyotrophic lateral sclerosis.
|
PLoS One
|
2012
|
1.09
|
24
|
A point mutation in the dynein heavy chain gene leads to striatal atrophy and compromises neurite outgrowth of striatal neurons.
|
Hum Mol Genet
|
2010
|
1.09
|
25
|
Histopathological analysis of skeletal muscle in patients with Parkinson's disease and 'dropped head'/'bent spine' syndrome.
|
Parkinsonism Relat Disord
|
2009
|
1.08
|
26
|
Late-onset motoneuron disease caused by a functionally modified AMPA receptor subunit.
|
Proc Natl Acad Sci U S A
|
2005
|
1.06
|
27
|
NF-κB is required for Smac mimetic-mediated sensitization of glioblastoma cells for γ-irradiation-induced apoptosis.
|
Mol Cancer Ther
|
2011
|
1.06
|
28
|
Linking neuron and skin: matrix metalloproteinases in amyotrophic lateral sclerosis (ALS).
|
J Neurol Sci
|
2009
|
1.05
|
29
|
Mice with a mutation in the dynein heavy chain 1 gene display sensory neuropathy but lack motor neuron disease.
|
Exp Neurol
|
2008
|
1.05
|
30
|
Phosphoinositide 3-kinases upregulate system xc(-) via eukaryotic initiation factor 2α and activating transcription factor 4 - A pathway active in glioblastomas and epilepsy.
|
Antioxid Redox Signal
|
2014
|
1.05
|
31
|
Grey-matter abnormalities in boys with Tourette syndrome: magnetic resonance imaging study using optimised voxel-based morphometry.
|
Br J Psychiatry
|
2006
|
1.04
|
32
|
Laryngospasm: an underdiagnosed symptom of X-linked spinobulbar muscular atrophy.
|
Neurology
|
2005
|
1.01
|
33
|
Cardiac involvement in patients with Becker muscular dystrophy: new diagnostic and pathophysiological insights by a CMR approach.
|
J Cardiovasc Magn Reson
|
2008
|
1.01
|
34
|
Inflammatory dysregulation of blood monocytes in Parkinson's disease patients.
|
Acta Neuropathol
|
2014
|
1.00
|
35
|
MRI-based functional neuroimaging in ALS: an update.
|
Amyotroph Lateral Scler
|
2009
|
0.99
|
36
|
A novel phosphorylation site mutation in profilin 1 revealed in a large screen of US, Nordic, and German amyotrophic lateral sclerosis/frontotemporal dementia cohorts.
|
Neurobiol Aging
|
2012
|
0.98
|
37
|
CSF concentrations of cAMP and cGMP are lower in patients with Creutzfeldt-Jakob disease but not Parkinson's disease and amyotrophic lateral sclerosis.
|
PLoS One
|
2012
|
0.98
|
38
|
Cerebrospinal fluid biomarkers of neurodegeneration in chronic neurological diseases.
|
Expert Rev Mol Diagn
|
2008
|
0.98
|
39
|
Low stability of Huntington muscle mitochondria against Ca2+ in R6/2 mice.
|
Ann Neurol
|
2006
|
0.97
|
40
|
NIPA1 polyalanine repeat expansions are associated with amyotrophic lateral sclerosis.
|
Hum Mol Genet
|
2012
|
0.97
|
41
|
Dynein mutations associated with hereditary motor neuropathies impair mitochondrial morphology and function with age.
|
Neurobiol Dis
|
2013
|
0.96
|
42
|
PGC-1α is a male-specific disease modifier of human and experimental amyotrophic lateral sclerosis.
|
Hum Mol Genet
|
2013
|
0.96
|
43
|
TDP-43 pathology and neuronal loss in amyotrophic lateral sclerosis spinal cord.
|
Acta Neuropathol
|
2014
|
0.96
|
44
|
Neuroanatomical patterns of cerebral white matter involvement in different motor neuron diseases as studied by diffusion tensor imaging analysis.
|
Amyotroph Lateral Scler
|
2012
|
0.96
|
45
|
Biochemical markers in CSF of ALS patients.
|
Curr Med Chem
|
2008
|
0.95
|
46
|
Proteome analysis of cerebrospinal fluid in amyotrophic lateral sclerosis (ALS).
|
Neurochem Res
|
2008
|
0.95
|
47
|
Brain metabolites in definite amyotrophic lateral sclerosis. A longitudinal proton magnetic resonance spectroscopy study.
|
J Neurol
|
2007
|
0.95
|
48
|
Quantification of brain atrophy in patients with myotonic dystrophy and proximal myotonic myopathy: a controlled 3-dimensional magnetic resonance imaging study.
|
Neurosci Lett
|
2003
|
0.95
|
49
|
Body fat distribution as a risk factor for cerebrovascular disease: an MRI-based body fat quantification study.
|
Cerebrovasc Dis
|
2013
|
0.94
|
50
|
Stages of granulovacuolar degeneration: their relation to Alzheimer's disease and chronic stress response.
|
Acta Neuropathol
|
2011
|
0.93
|
51
|
A novel optineurin truncating mutation and three glaucoma-associated missense variants in patients with familial amyotrophic lateral sclerosis in Germany.
|
Neurobiol Aging
|
2012
|
0.93
|
52
|
Emotional responding in amyotrophic lateral sclerosis.
|
J Neurol
|
2005
|
0.92
|
53
|
Effects of mitochondrial dysfunction on the immunological properties of microglia.
|
J Neuroinflammation
|
2010
|
0.92
|
54
|
Amyotrophic lateral sclerosis: disease stage related changes of tau protein and S100 beta in cerebrospinal fluid and creatine kinase in serum.
|
Neurosci Lett
|
2003
|
0.92
|
55
|
Diffusion tensor imaging and tractwise fractional anisotropy statistics: quantitative analysis in white matter pathology.
|
Biomed Eng Online
|
2007
|
0.92
|
56
|
A large genome scan for rare CNVs in amyotrophic lateral sclerosis.
|
Hum Mol Genet
|
2010
|
0.92
|
57
|
Retinal single-layer analysis in Parkinsonian syndromes: an optical coherence tomography study.
|
J Neural Transm (Vienna)
|
2013
|
0.91
|
58
|
Intersubject variability in the analysis of diffusion tensor images at the group level: fractional anisotropy mapping and fiber tracking techniques.
|
Magn Reson Imaging
|
2008
|
0.91
|
59
|
Quantification of human body fat tissue percentage by MRI.
|
NMR Biomed
|
2011
|
0.91
|
60
|
Whole brain-based computerized neuroimaging in ALS and other motor neuron disorders.
|
Amyotroph Lateral Scler
|
2008
|
0.91
|
61
|
High-caloric food supplements in the treatment of amyotrophic lateral sclerosis: a prospective interventional study.
|
Amyotroph Lateral Scler Frontotemporal Degener
|
2013
|
0.90
|
62
|
Rasagiline alone and in combination with riluzole prolongs survival in an ALS mouse model.
|
J Neurol
|
2004
|
0.90
|
63
|
In vivo quantification of spinal and bulbar motor neuron degeneration in the G93A-SOD1 transgenic mouse model of ALS by T2 relaxation time and apparent diffusion coefficient.
|
Exp Neurol
|
2006
|
0.90
|
64
|
Extracellular vesicle sorting of α-Synuclein is regulated by sumoylation.
|
Acta Neuropathol
|
2015
|
0.90
|
65
|
Mutual exacerbation of peroxisome proliferator-activated receptor γ coactivator 1α deregulation and α-synuclein oligomerization.
|
Ann Neurol
|
2014
|
0.90
|
66
|
Summary of cerebrospinal fluid routine parameters in neurodegenerative diseases.
|
J Neurol
|
2010
|
0.90
|
67
|
Proteome analysis reveals candidate markers of disease progression in amyotrophic lateral sclerosis (ALS).
|
Neurosci Lett
|
2009
|
0.89
|
68
|
The Edinburgh Cognitive and Behavioural Amyotrophic Lateral Sclerosis Screen: a cross-sectional comparison of established screening tools in a German-Swiss population.
|
Amyotroph Lateral Scler Frontotemporal Degener
|
2014
|
0.89
|
69
|
Systemic dysregulation of TDP-43 binding microRNAs in amyotrophic lateral sclerosis.
|
Acta Neuropathol Commun
|
2013
|
0.89
|
70
|
Neuroimaging of multimodal sensory stimulation in amyotrophic lateral sclerosis.
|
J Neurol Neurosurg Psychiatry
|
2010
|
0.89
|
71
|
Emotional adjustment in amyotrophic lateral sclerosis (ALS).
|
J Neurol
|
2011
|
0.89
|
72
|
Levodopa-induced striatal activation in Parkinson's disease: a functional MRI study.
|
Parkinsonism Relat Disord
|
2009
|
0.88
|
73
|
H63D polymorphism in HFE is not associated with amyotrophic lateral sclerosis.
|
Neurobiol Aging
|
2012
|
0.87
|
74
|
Novel mutation in the ALS2 gene in juvenile amyotrophic lateral sclerosis.
|
Ann Neurol
|
2005
|
0.86
|
75
|
Soluble beta-amyloid precursor protein is related to disease progression in amyotrophic lateral sclerosis.
|
PLoS One
|
2011
|
0.86
|
76
|
Severe sensorimotor neuropathy after intake of highest dosages of vitamin B6.
|
Neuromuscul Disord
|
2007
|
0.86
|
77
|
Differential diagnostic value of eye movement recording in PSP-parkinsonism, Richardson's syndrome, and idiopathic Parkinson's disease.
|
J Neurol
|
2009
|
0.86
|
78
|
Brain responses to emotional stimuli in patients with amyotrophic lateral sclerosis (ALS).
|
J Neurol
|
2007
|
0.86
|
79
|
Eye movement impairments in Parkinson's disease: possible role of extradopaminergic mechanisms.
|
BMC Neurol
|
2012
|
0.86
|
80
|
On the decline and etiology of high-incidence motor system disease in West Papua (southwest New Guinea).
|
Mov Disord
|
2005
|
0.85
|
81
|
Limited role of free TDP-43 as a diagnostic tool in neurodegenerative diseases.
|
Amyotroph Lateral Scler Frontotemporal Degener
|
2014
|
0.85
|
82
|
Metabolic progression markers of neurodegeneration in the transgenic G93A-SOD1 mouse model of amyotrophic lateral sclerosis.
|
Eur J Neurosci
|
2007
|
0.85
|
83
|
Mutations in cytoplasmic dynein lead to a Huntington's disease-like defect in energy metabolism of brown and white adipose tissues.
|
Biochim Biophys Acta
|
2010
|
0.85
|
84
|
Age-dependent changes in MRI of motor brain stem nuclei in a mouse model of ALS.
|
Neuroreport
|
2004
|
0.85
|
85
|
Neurofilament heavy-chain NfH(SMI35) in cerebrospinal fluid supports the differential diagnosis of Parkinsonian syndromes.
|
Mov Disord
|
2006
|
0.84
|
86
|
Functional connectivity within the default mode network is associated with saccadic accuracy in Parkinson's disease: a resting-state FMRI and videooculographic study.
|
Brain Connect
|
2013
|
0.84
|
87
|
A new MRI rating scale for progressive supranuclear palsy and multiple system atrophy: validity and reliability.
|
J Neurol Neurosurg Psychiatry
|
2011
|
0.84
|
88
|
MMP-2 and MMP-9 are elevated in spinal cord and skin in a mouse model of ALS.
|
J Neurol Sci
|
2010
|
0.84
|
89
|
Can lesions to the motor cortex induce amyotrophic lateral sclerosis?
|
J Neurol
|
2013
|
0.84
|
90
|
Mechanisms of disease: motoneuron disease aggravated by transgenic expression of a functionally modified AMPA receptor subunit.
|
Ann N Y Acad Sci
|
2005
|
0.84
|
91
|
Comparison of smooth pursuit eye movement deficits in multiple system atrophy and Parkinson's disease.
|
J Neurol
|
2009
|
0.84
|
92
|
Cortical plasticity in amyotrophic lateral sclerosis: motor imagery and function.
|
Neurorehabil Neural Repair
|
2007
|
0.84
|
93
|
C9orf72 and UNC13A are shared risk loci for amyotrophic lateral sclerosis and frontotemporal dementia: a genome-wide meta-analysis.
|
Ann Neurol
|
2014
|
0.83
|
94
|
Deep brain stimulation and behavioural changes: is comedication the most important factor?
|
Neurodegener Dis
|
2011
|
0.83
|
95
|
Quality of life in fatal disease: the flawed judgement of the social environment.
|
J Neurol
|
2013
|
0.83
|
96
|
Developmental and functional nature of human iPSC derived motoneurons.
|
Stem Cell Rev
|
2013
|
0.83
|
97
|
Connective tissue disorders in dissections of the carotid or vertebral arteries.
|
J Clin Neurosci
|
2008
|
0.83
|
98
|
Only subtle cognitive deficits in non-bulbar amyotrophic lateral sclerosis patients.
|
J Neurol
|
2005
|
0.83
|
99
|
The SETX missense variation spectrum as evaluated in patients with ALS4-like motor neuron diseases.
|
Neurogenetics
|
2012
|
0.83
|
100
|
Implementation of a population-based epidemiological rare disease registry: study protocol of the amyotrophic lateral sclerosis (ALS)--registry Swabia.
|
BMC Neurol
|
2013
|
0.83
|
101
|
The use of P300-based BCIs in amyotrophic lateral sclerosis: from augmentative and alternative communication to cognitive assessment.
|
Brain Behav
|
2012
|
0.83
|
102
|
Frequency of a tau genotype in amyotrophic lateral sclerosis.
|
J Neurol Sci
|
2005
|
0.82
|
103
|
Vacuolization correlates with spin-spin relaxation time in motor brainstem nuclei and behavioural tests in the transgenic G93A-SOD1 mouse model of ALS.
|
Eur J Neurosci
|
2007
|
0.82
|
104
|
Fumaric acid esters stimulate astrocytic VEGF expression through HIF-1α and Nrf2.
|
PLoS One
|
2013
|
0.82
|
105
|
Do eye movement impairments in patients with small vessel cerebrovascular disease depend on lesion load or on cognitive deficits? A video-oculographic and MRI study.
|
J Neurol
|
2014
|
0.82
|
106
|
The dynactin p150 subunit: cell biology studies of sequence changes found in ALS/MND and Parkinsonian syndromes.
|
J Neural Transm (Vienna)
|
2012
|
0.81
|
107
|
Serum Vitamin D Concentrations and Cognitive Function in a Population-Based Study among Older Adults in South Germany.
|
J Alzheimers Dis
|
2015
|
0.81
|
108
|
Cardiovascular magnetic resonance imaging (CMR) reveals characteristic pattern of myocardial damage in patients with mitochondrial myopathy.
|
Clin Res Cardiol
|
2011
|
0.81
|
109
|
Intracerebral hemorrhage in a patient with glycogenosis type II (Pompe disease): is there a pathophysiological relationship?
|
Muscle Nerve
|
2008
|
0.81
|
110
|
Complementary image analysis of diffusion tensor imaging and 3-dimensional t1-weighted imaging: white matter analysis in amyotrophic lateral sclerosis.
|
J Neuroimaging
|
2011
|
0.81
|
111
|
Parkinson's disease-like midbrain hyperechogenicity is frequent in amyotrophic lateral sclerosis.
|
J Neurol
|
2012
|
0.81
|
112
|
Primary progressive aphasia accompanied by environmental sound agnosia: a neuropsychological, MRI and PET study.
|
Psychiatry Res
|
2006
|
0.81
|
113
|
Cerebral white matter alterations in idiopathic restless legs syndrome, as measured by diffusion tensor imaging.
|
Mov Disord
|
2008
|
0.81
|
114
|
Neurotransplantation in mice: the concorde-like position ensures minimal cell leakage and widespread distribution of cells transplanted into the cisterna magna.
|
Neurosci Lett
|
2007
|
0.81
|
115
|
Evaluating multicenter DTI data in Huntington's disease on site specific effects: An ex post facto approach.
|
Neuroimage Clin
|
2013
|
0.81
|
116
|
Motor neuron disease: urgently needed-biomarkers for amyotrophic lateral sclerosis.
|
Nat Rev Neurol
|
2011
|
0.81
|
117
|
MR-pathologic comparison of the upper spinal cord in different motor neuron diseases.
|
Eur Neurol
|
2005
|
0.81
|
118
|
Candidate biomarkers of chronic inflammatory demyelinating polyneuropathy (CIDP): proteome analysis of cerebrospinal fluid.
|
J Neuroimmunol
|
2009
|
0.81
|
119
|
Imaging of activated microglia with PET and [11C]PK 11195 in corticobasal degeneration.
|
Mov Disord
|
2004
|
0.81
|
120
|
Differential regulation of 5' splice variants of the glutamate transporter EAAT2 in an in vivo model of chemical hypoxia induced by 3-nitropropionic acid.
|
J Neurosci Res
|
2003
|
0.81
|
121
|
Percutaneous endoscopic gastrostomy in amyotrophic lateral sclerosis: a prospective observational study.
|
J Neurol
|
2015
|
0.81
|
122
|
Live and let die: existential decision processes in a fatal disease.
|
J Neurol
|
2014
|
0.81
|
123
|
Chemical hypoxia facilitates alternative splicing of EAAT2 in presymptomatic APP23 transgenic mice.
|
Neurochem Res
|
2007
|
0.81
|
124
|
Cerebrospinal fluid markers of idiopathic intracranial hypertension: is the renin-angiotensinogen system involved?
|
Cephalalgia
|
2010
|
0.80
|
125
|
Longitudinal effects of noninvasive positive-pressure ventilation in patients with amyotrophic lateral sclerosis.
|
Am J Phys Med Rehabil
|
2003
|
0.80
|
126
|
Cerebrospinal fluid erythropoietin (EPO) in amyotrophic lateral sclerosis.
|
Neurosci Lett
|
2007
|
0.80
|
127
|
Signs of impaired selective attention in patients with amyotrophic lateral sclerosis.
|
J Neurol
|
2008
|
0.80
|
128
|
Directional colour encoding of the human thalamus by diffusion tensor imaging.
|
Neurosci Lett
|
2008
|
0.80
|
129
|
Adipose Tissue Distribution Predicts Survival in Amyotrophic Lateral Sclerosis.
|
PLoS One
|
2013
|
0.80
|
130
|
Eye-tracking controlled cognitive function tests in patients with amyotrophic lateral sclerosis: a controlled proof-of-principle study.
|
J Neurol
|
2015
|
0.80
|
131
|
Erythropoietin in cerebrospinal fluid: age-related reference values and relevance in neurological disease.
|
Neurochem Res
|
2007
|
0.80
|
132
|
Efficient processing of Alzheimer's disease amyloid-Beta peptides by neuroectodermally converted mesenchymal stem cells.
|
Stem Cells Dev
|
2010
|
0.79
|
133
|
Fast diffusion tensor magnetic resonance imaging of the mouse brain at ultrahigh-field: aiming at cohort studies.
|
PLoS One
|
2012
|
0.79
|
134
|
Additional resources and the default mode network: Evidence of increased connectivity and decreased white matter integrity in amyotrophic lateral sclerosis.
|
Amyotroph Lateral Scler Frontotemporal Degener
|
2014
|
0.79
|
135
|
Micronutrients supplementation and nutritional status in cognitively impaired elderly persons: a two-month open label pilot study.
|
Nutr J
|
2013
|
0.79
|
136
|
A biochemical marker panel in MRI-proven hyperacute ischemic stroke-a prospective study.
|
BMC Neurol
|
2012
|
0.79
|
137
|
Different regional brain volume loss in pure and complicated hereditary spastic paraparesis: a voxel-based morphometric study.
|
Amyotroph Lateral Scler
|
2007
|
0.79
|
138
|
Rate of change in early Huntington's disease: a clinicometric analysis.
|
Mov Disord
|
2011
|
0.79
|
139
|
Dietary antioxidants and dementia in a population-based case-control study among older people in South Germany.
|
J Alzheimers Dis
|
2012
|
0.79
|
140
|
Neuroimaging of motor neuron diseases.
|
Ther Adv Neurol Disord
|
2012
|
0.78
|
141
|
Camptocormia in Parkinson's disease: a review of the literature.
|
Neurodegener Dis
|
2011
|
0.78
|
142
|
The cerebro-morphological fingerprint of a progeroid syndrome: white matter changes correlate with neurological symptoms in xeroderma pigmentosum.
|
PLoS One
|
2012
|
0.78
|
143
|
Hypercapnia is a possible determinant of the function of the blood-cerebrospinal fluid barrier in amyotrophic lateral sclerosis.
|
Neurochem Res
|
2010
|
0.78
|
144
|
Protease-resistant SOD1 aggregates in amyotrophic lateral sclerosis demonstrated by paraffin-embedded tissue (PET) blot.
|
Acta Neuropathol Commun
|
2014
|
0.78
|
145
|
A mutation in the dynein heavy chain gene compensates for energy deficit of mutant SOD1 mice and increases potentially neuroprotective IGF-1.
|
Mol Neurodegener
|
2011
|
0.78
|
146
|
Impact of the control for corrupted diffusion tensor imaging data in comparisons at the group level: an application in Huntington disease.
|
Biomed Eng Online
|
2014
|
0.78
|
147
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