Sfoglia per Autore
TREX1 C-terminal frameshift mutations in the systemic variant of retinal vasculopathy with cerebral leukodystrophy
2015 Difrancesco, J; Novara, F; Zuffardi, O; Forlino, A; Gioia, R; Cossu, F; Bolognesi, M; Andreoni, S; Saracchi, E; Frigeni, B; Stellato, T; Tolnay, M; Winkler, D; Remida, P; Isimbaldi, G; Ferrarese, C
Reduced expression of the chaperone-mediated autophagy carrier hsc70 protein in lymphomonocytes of patients with Parkinson's disease
2014 Sala, G; Stefanoni, G; Arosio, A; Riva, C; Melchionda, L; Saracchi, E; Fermi, S; Brighina, L; Ferrarese, C
A novel heterozygous SETX mutation in a patient presenting with chorea and motor neuron disease
2014 Saracchi, E; Castelli, M; Bassi, M; Brighina, E; Cereda, D; Marzorati, L; Patassini, M; Appollonio, I; Ferrarese, C; Brighina, L
Novel neurofibromatosis type 2 mutation presenting with status epilepticus
2014 DI FRANCESCO, J; Sestini, R; Cossu, F; Bolognesi, M; Sala, E; Mariani, S; Saracchi, E; Papi, L; Ferrarese, C
Fahr's disease linked to a novel SLC20A2 gene mutation manifesting with dynamic aphasia
2014 Brighina, L; Saracchi, E; Ferri, F; Gagliardi, M; Tarantino, P; Morzenti, S; Musarra, M; Patassini, M; Annesi, G; Ferrarese, C
Study of alpha-synuclein and its catabolic pathways in lymphomonocytes of patients with Parkinson's disease
2013 Sala, G; Stefanoni, G; Arosio, A; Riva, C; Marinig, D; Saracchi, E; Fermi, S; Brighina, L; Ferrarese, C
Reduced expression of hsc70 protein in lymphomonocytes of patients with Parkinson's disease
2013 Stefanoni, G; Sala, G; Arosio, A; Riva, C; Marinig, D; Saracchi, E; Brighina, L; Ferrarese, C
A case of Leber hereditary optic neuropathy plus dystonia caused by G14459A mitochondrial mutation
2013 Saracchi, E; DI FRANCESCO, J; Brighina, L; Marzorati, L; Curtò, N; Lamperti, C; Carrara, F; Zeviani, M; Ferrarese, C
Analysis of vesicular monoamine transporter 2 polymorphisms in Parkinson's disease
2013 Brighina, L; Riva, C; Bertola, F; Saracchi, E; Fermi, S; Goldwurm, S; Ferrarese, C
Chaperone mediated autophagy in Parkinson's disease: Study in peripheral blood cells from patients and in a cellular model
2011 Stefanoni, G; Sala, G; Arosio, A; Melchionda, L; Saracchi, E; Fermi, S; Brighina, L; Ferrarese, C
Dysfunction of chaperone-mediated autophagy in lymphomonocytes from patients with Parkinson's disease and in a cellular model
2011 Stefanoni, G; Sala, G; Arosio, A; Melchionda, L; Saracchi, E; Fermi, S; Brighina, L; Ferrarese, C
Assessment of chaperone-mediated autophagy in circulating lymphomonocytes of patients with Parkinson disease
2011 Sala, G; Stefanoni, G; Arosio, A; Melchionda, L; Saracchi, E; Fermi, S; Brighina, L; Ferrarese, C
I sintomi non motori nella malattia di Parkinson
2011 Saracchi, E; Appollonio, I
Anti-Aβ autoantibodies in the CSF of a patient with CAA-related inflammation: a case report
2011 DI FRANCESCO, J; Brioschi, M; Brighina, L; Ruffmann, C; Saracchi, E; Costantino, G; Galimberti, G; Conti, E; Curtò, N; Marzorati, L; Remida, P; Tagliavini, F; Savoiardo, M; Ferrarese, C
Cerebellar hematoma in a carrier of the A3243G MELAS mutation
2011 Saracchi, E; Tremolizzo, L; DI FRANCESCO, J; Brighina, L; Costantino, G; Frigeni, B; Brioschi, M; Piatti, M; Fumagalli, L; Marzorati, L; Curtò, N; Ferrarese, C
Association analysis of PARP1 polymorphisms with Parkinson's disease
2011 Brighina, L; Riva, C; Bertola, F; Fermi, S; Saracchi, E; Piolti, R; Goldwurm, S; Pezzoli, G; Ferrarese, C
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