Published in Brain on November 14, 2006
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Temporal discrimination threshold with healthy aging. Neurobiol Aging (2016) 0.77
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A headset method for measuring the visual temporal discrimination threshold in cervical dystonia. Tremor Other Hyperkinet Mov (N Y) (2014) 0.75
DYT1 dystonia increases risk taking in humans. Elife (2016) 0.75
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Theta burst stimulation of the human motor cortex. Neuron (2005) 8.33
An SCN9A channelopathy causes congenital inability to experience pain. Nature (2006) 7.01
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A common LRRK2 mutation in idiopathic Parkinson's disease. Lancet (2005) 5.81
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DCTN1 mutations in Perry syndrome. Nat Genet (2009) 3.87
Mitochondrial import and enzymatic activity of PINK1 mutants associated to recessive parkinsonism. Hum Mol Genet (2005) 3.76
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SNCA variants are associated with increased risk for multiple system atrophy. Ann Neurol (2009) 3.55
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Clinical and molecular phenotype of Aicardi-Goutieres syndrome. Am J Hum Genet (2007) 2.81
Stereotypies: a critical appraisal and suggestion of a clinically useful definition. Mov Disord (2011) 2.76
Racial bias reduces empathic sensorimotor resonance with other-race pain. Curr Biol (2010) 2.76
Transcranial magnetic stimulation highlights the sensorimotor side of empathy for pain. Nat Neurosci (2005) 2.75
Mutations in INPP5E, encoding inositol polyphosphate-5-phosphatase E, link phosphatidyl inositol signaling to the ciliopathies. Nat Genet (2009) 2.72
Clinical and molecular genetics of Leber's congenital amaurosis: a multicenter study of Italian patients. Invest Ophthalmol Vis Sci (2007) 2.69
Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome. Am J Hum Genet (2008) 2.65
ATP13A2 mutations (PARK9) cause neurodegeneration with brain iron accumulation. Mov Disord (2010) 2.47
Loss of sight and sound. Could it be the hip? Lancet (2009) 2.43
Parkin disease: a phenotypic study of a large case series. Brain (2003) 2.41
Distinguishing SWEDDs patients with asymmetric resting tremor from Parkinson's disease: a clinical and electrophysiological study. Mov Disord (2010) 2.36
Hereditary haemochromatosis is unlikely to cause movement disorders--a critical review. J Neurol (2004) 2.17
Hashimoto's encephalopathy: epidemiologic data and pathogenetic considerations. J Neurol Sci (2004) 2.02
Parkes Weber syndrome, vein of Galen aneurysmal malformation, and other fast-flow vascular anomalies are caused by RASA1 mutations. Hum Mutat (2008) 2.00
Translation initiator EIF4G1 mutations in familial Parkinson disease. Am J Hum Genet (2011) 2.00
Functional (psychogenic) symptoms in Parkinson's disease. Mov Disord (2013) 1.99
Pain as a nonmotor symptom of Parkinson disease: evidence from a case-control study. Arch Neurol (2008) 1.96
Mutations in the autoregulatory domain of β-tubulin 4a cause hereditary dystonia. Ann Neurol (2013) 1.90
AHI1 is required for photoreceptor outer segment development and is a modifier for retinal degeneration in nephronophthisis. Nat Genet (2010) 1.89
CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders. Am J Hum Genet (2007) 1.82
Mutations in ANO3 cause dominant craniocervical dystonia: ion channel implicated in pathogenesis. Am J Hum Genet (2012) 1.78
Pallidal stimulation improves pantothenate kinase-associated neurodegeneration. Ann Neurol (2005) 1.74
Evolutionarily assembled cis-regulatory module at a human ciliopathy locus. Science (2012) 1.74
Functional (psychogenic) movement disorders: merging mind and brain. Lancet Neurol (2012) 1.72
Mutations in SLC30A10 cause parkinsonism and dystonia with hypermanganesemia, polycythemia, and chronic liver disease. Am J Hum Genet (2012) 1.71
Natural history and syndromic associations of orthostatic tremor: a review of 41 patients. Mov Disord (2004) 1.69
Autosomal recessive, DYT2-like primary torsion dystonia: a new family. Neurology (2003) 1.69
Progressive delayed-onset dystonia after cerebral anoxic insult in adults. Mov Disord (2002) 1.69
Cerebellar stimulation fails to modulate motor cortex plasticity in writing dystonia. Mov Disord (2014) 1.65
A comparative study of primary and secondary hemifacial spasm. Arch Neurol (2006) 1.65
The focal dystonias: current views and challenges for future research. Mov Disord (2013) 1.62
Neuropathy and levodopa in Parkinson's disease: evidence from a multicenter study. Mov Disord (2013) 1.62
GLUT1 mutations are a cause of paroxysmal exertion-induced dyskinesias and induce hemolytic anemia by a cation leak. J Clin Invest (2008) 1.60
Lateral trunk flexion in Parkinson's disease: EMG features disclose two different underlying pathophysiological mechanisms. J Neurol (2010) 1.57
Widespread Lewy body and tau accumulation in childhood and adult onset dystonia-parkinsonism cases with PLA2G6 mutations. Neurobiol Aging (2010) 1.56
Early-onset L-dopa-responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutations. Mov Disord (2010) 1.56
Comprehensive analysis of the LRRK2 gene in sixty families with Parkinson's disease. Eur J Hum Genet (2006) 1.56
Pisa syndrome without neuroleptic exposure in a patient with Parkinson's disease: case report. Mov Disord (2006) 1.56
CEP41 is mutated in Joubert syndrome and is required for tubulin glutamylation at the cilium. Nat Genet (2012) 1.54
The natural history of Unverricht-Lundborg disease: a report of eight genetically proven cases. Mov Disord (2008) 1.53
Endothelial nitric oxide synthase (Glu298Asp) polymorphism is an independent risk factor for migraine with aura. Headache (2006) 1.52
Mutant Pink1 induces mitochondrial dysfunction in a neuronal cell model of Parkinson's disease by disturbing calcium flux. J Neurochem (2009) 1.52
Patients with scans without evidence of dopaminergic deficit: a long-term follow-up study. Mov Disord (2014) 1.51
Clinical and subclinical dopaminergic dysfunction in PARK6-linked parkinsonism: an 18F-dopa PET study. Ann Neurol (2002) 1.51
Representation of body identity and body actions in extrastriate body area and ventral premotor cortex. Nat Neurosci (2006) 1.50
CC2D2A mutations in Meckel and Joubert syndromes indicate a genotype-phenotype correlation. Hum Mutat (2009) 1.48
In vivo assessment of brain monoamine systems in parkin gene carriers: a PET study. Exp Neurol (2010) 1.47
Botulinum toxin injections reduce associative plasticity in patients with primary dystonia. Mov Disord (2011) 1.47
Does statin in the acute phase of ischemic stroke improve outcome after intravenous thrombolysis? A retrospective study. J Neurol Sci (2011) 1.46
Moving toward "laboratory-supported" criteria for psychogenic tremor. Mov Disord (2011) 1.45
Patients with adult-onset dystonic tremor resembling parkinsonian tremor have scans without evidence of dopaminergic deficit (SWEDDs). Mov Disord (2007) 1.44
PRRT2 gene mutations: from paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine. Neurology (2012) 1.44
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The arginine growth hormone stimulation test in bradykinetic-rigid parkinsonisms. Mov Disord (2008) 1.43
MKS3/TMEM67 mutations are a major cause of COACH Syndrome, a Joubert Syndrome related disorder with liver involvement. Hum Mutat (2009) 1.43
The body in the brain revisited. Exp Brain Res (2009) 1.42
Syndromes of neurodegeneration with brain iron accumulation (NBIA): an update on clinical presentations, histological and genetic underpinnings, and treatment considerations. Mov Disord (2011) 1.41
The entity of young onset primary cervical dystonia. Mov Disord (2007) 1.41
Independent and joint effects of the MAPT and SNCA genes in Parkinson disease. Ann Neurol (2011) 1.40
Day-7 modified Rankin Scale score as the best measure of the thrombolysis direct effect on stroke? J Thromb Thrombolysis (2013) 1.39
Mapping implied body actions in the human motor system. J Neurosci (2006) 1.38
Learning potentiates neurophysiological and behavioral placebo analgesic responses. Pain (2008) 1.35
Neurological principles and rehabilitation of action disorders: rehabilitation interventions. Neurorehabil Neural Repair (2011) 1.35
Tremor--some controversial aspects. Mov Disord (2010) 1.35
Complex movement disorders at disease onset in childhood narcolepsy with cataplexy. Brain (2011) 1.35
The progression of non-motor symptoms in Parkinson's disease and their contribution to motor disability and quality of life. J Neurol (2012) 1.34
Myoclonus-dystonia syndrome: epsilon-sarcoglycan mutations and phenotype. Ann Neurol (2002) 1.33
Novel TMEM67 mutations and genotype-phenotype correlates in meckelin-related ciliopathies. Hum Mutat (2010) 1.32
Selective impairment of hand mental rotation in patients with focal hand dystonia. Brain (2005) 1.31
Dopamine and performance in a reinforcement learning task: evidence from Parkinson's disease. Brain (2012) 1.30
Effect of balance training on postural instability in patients with idiopathic Parkinson's disease. Neurorehabil Neural Repair (2010) 1.30
Absence of embodied empathy during pain observation in Asperger syndrome. Biol Psychiatry (2008) 1.30
Patients with focal arm dystonia have increased sensitivity to slow-frequency repetitive TMS of the dorsal premotor cortex. Brain (2003) 1.30
Clinical approach to Parkinson's disease: features, diagnosis, and principles of management. Cold Spring Harb Perspect Med (2012) 1.30
Abnormalities in motor cortical plasticity differentiate manifesting and nonmanifesting DYT1 carriers. Mov Disord (2006) 1.28