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E. Saracchi · SciRah

Researcher profile · Semantic Scholar

E. Saracchi

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E. Saracchi — researcher profile on SciRah

h-index: 10
Works: 18
Citations: 475

Most-cited papers

Anti-Aβ autoantibodies in the CSF of a patient with CAA-related inflammation: A case report
J. DiFrancesco, M. Brioschi, L. Brighina, C. Ruffmann +10 more
2011Neurology117 citations
Semantic Scholar
Reduced expression of the chaperone-mediated autophagy carrier hsc70 protein in lymphomonocytes of patients with Parkinson's disease.
G. Sala, G. Stefanoni, A. Arosio, C. Riva +5 more
2014Brain Research70 citations
Semantic Scholar
Analysis of vesicular monoamine transporter 2 polymorphisms in Parkinson’s disease
L. Brighina, C. Riva, F. Bertola, E. Saracchi +3 more
2013Neurobiology of Aging69 citations Open access
Semantic Scholar
TREX1 C-terminal frameshift mutations in the systemic variant of retinal vasculopathy with cerebral leukodystrophy
J. DiFrancesco, F. Novara, O. Zuffardi, A. Forlino +12 more
2015Neurological Sciences53 citations
Semantic Scholar
Vesicular monoamine transporter 2 mRNA levels are reduced in platelets from patients with Parkinson’s disease
G. Sala, L. Brighina, E. Saracchi, S. Fermi +4 more
2010Journal of neural transmission53 citations
Semantic Scholar
Emerging candidate biomarkers for Parkinson's disease: a review.
E. Saracchi, S. Fermi, L. Brighina
2014Aging and Disease47 citations Open access
Semantic Scholar
Fahr's Disease Linked to a Novel SLC20A2 Gene Mutation Manifesting with Dynamic Aphasia
L. Brighina, E. Saracchi, F. Ferri, M. Gagliardi +6 more
2014Neurodegenerative Diseases17 citations
Semantic Scholar
A case of Leber hereditary optic neuropathy plus dystonia caused by G14459A mitochondrial mutation
E. Saracchi, J. DiFrancesco, L. Brighina, L. Marzorati +5 more
2013Neurological Sciences17 citations
Semantic Scholar
Novel neurofibromatosis type 2 mutation presenting with status epilepticus.
J. DiFrancesco, R. Sestini, F. Cossu, M. Bolognesi +5 more
2014Epileptic disorders10 citations
Semantic Scholar
A novel heterozygous SETX mutation in a patient presenting with chorea and motor neuron disease
E. Saracchi, Marianna Castelli, M. T. Bassi, E. Brighina +6 more
2014Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration10 citations
Semantic Scholar
Association analysis of PARP1 polymorphisms with Parkinson’s disease
L. Brighina, C. Riva, F. Bertola, S. Fermi +5 more
2011Parkinsonism & Related Disorders10 citations Open access
Semantic Scholar
Cerebellar hematoma in a carrier of the A3243G MELAS mutation
E. Saracchi, L. Tremolizzo, J. DiFrancesco, L. Brighina +8 more
2011Neurological Sciences2 citations
Semantic Scholar
Comparison between MEPs before and after PAS on homologous hemisphere disclosed a trend toward an increased of amplitude, but without reaching statistical significance for both ABP and FDI
tremor—N. Bovina, A. Cagnani, P. Maggio, F. Fiacco +13 more
20180 citations
Semantic Scholar
Study of alpha-synuclein and its catabolic pathways in lymphomonocytes of patients with Parkinson's disease
G. Sala, G. Stefanoni, A. Arosio, C. Riva +5 more
20130 citations
Semantic Scholar
Reduced expression of hsc70 protein in lymphomonocytes of patients with Parkinson's disease
G. Stefanoni, G. Sala, A. Arosio, C. Riva +4 more
20130 citations
Semantic Scholar
Chaperone mediated autophagy in Parkinson's disease: Study in peripheral blood cells from patients and in a cellular model
G. Stefanoni, G. Sala, A. Arosio, L. Melchionda +4 more
20110 citations
Semantic Scholar
Assessment of chaperone-mediated autophagy in circulating lymphomonocytes of patients with Parkinson disease
G. Sala, G. Stefanoni, A. Arosio, L. Melchionda +4 more
20110 citations
Semantic Scholar
Dysfunction of chaperone-mediated autophagy in lymphomonocytes from patients with Parkinson's disease and in a cellular model
G. Stefanoni, G. Sala, A. Arosio, L. Melchionda +4 more
20110 citations
Semantic Scholar

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