Michel Borg

Author PubWeight™ 13.86^‹?›

Rank	Title	Journal	Year	PubWeight™‹?›
1	Mutations in the Na+/K+ -ATPase alpha3 gene ATP1A3 are associated with rapid-onset dystonia parkinsonism.	Neuron	2004	3.59
2	The phenotypic spectrum of rapid-onset dystonia-parkinsonism (RDP) and mutations in the ATP1A3 gene.	Brain	2007	1.73
3	Mutational analysis of the PINK1 gene in early-onset parkinsonism in Europe and North Africa.	Brain	2006	1.41
4	Complex partial status epilepticus revealing anti-NMDA receptor encephalitis.	Epileptic Disord	2009	1.24
5	Disease severity and progression in progressive supranuclear palsy and multiple system atrophy: validation of the NNIPPS--Parkinson Plus Scale.	PLoS One	2011	1.15
6	Effect of subthalamic nucleus stimulation on obsessive-compulsive disorder in a patient with Parkinson disease. Case report.	J Neurosurg	2004	0.98
7	LRRK2 exon 41 mutations in sporadic Parkinson disease in Europeans.	Arch Neurol	2007	0.97
8	Singular DYT6 phenotypes in association with new THAP1 frameshift mutations.	Mov Disord	2011	0.84
9	Frequency of the LRRK2 G2019S mutation in siblings with Parkinson's disease.	Neurodegener Dis	2007	0.78
10	Deep brain stimulation of the ventral intermediate thalamic nucleus for severe tremor in anti-MAG neuropathy.	Mov Disord	2009	0.78
11	Substitutions at residue 211 in the prion protein drive a switch between CJD and GSS syndrome, a new mechanism governing inherited neurodegenerative disorders.	Hum Mol Genet	2012	0.78