Sara Bonato

Author PubWeight™ 9.78^‹?›

Rank	Title	Journal	Year	PubWeight™‹?›
1	Genotype and phenotype characterization in a large dystrophinopathic cohort with extended follow-up.	J Neurol	2011	1.28
2	Gait pattern in Duchenne muscular dystrophy.	Gait Posture	2008	1.16
3	Reliability and validity of the International Cooperative Ataxia Rating Scale: a study in 156 spinocerebellar ataxia patients.	Mov Disord	2006	1.10
4	A wide spectrum of clinical, neurophysiological and neuroradiological abnormalities in a family with a novel CACNA1A mutation.	J Neurol Neurosurg Psychiatry	2010	1.04
5	Frequency and characterisation of anoctamin 5 mutations in a cohort of Italian limb-girdle muscular dystrophy patients.	Neuromuscul Disord	2012	0.96
6	Nitric oxide donor and non steroidal anti inflammatory drugs as a therapy for muscular dystrophies: evidence from a safety study with pilot efficacy measures in adult dystrophic patients.	Pharmacol Res	2012	0.94
7	Defective autophagy in spastizin mutated patients with hereditary spastic paraparesis type 15.	Brain	2013	0.90
8	Mitochondrial DNA G8363A mutation in the tRNA Lys gene: clinical, biochemical and pathological study.	J Neurol Sci	2009	0.89
9	Eight novel mutations in SPG4 in a large sample of patients with hereditary spastic paraplegia.	Arch Neurol	2006	0.86
10	Characterization of two novel SETX mutations in AOA2 patients reveals aspects of the pathophysiological role of senataxin.	Neurogenetics	2009	0.81