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Prodotti della tipologia (ordinati per Data di deposito in Decrescente ordine): 1 a 20 di 125634
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TitoloData di depositoAutore(i)
Complex movement disorders in primary antiphospholipid syndrome: A case report7-lug-2020Carecchio, M.; Comi, C.; Varrasi, C.; Stecco, A.; Sainaghi, P. P.; Bhatia, K.; Carriero, A.; Cantello, R.; Monaco, F.
Progranulin plasma levels as potential biomarker for the identification of GRN deletion carriers. A case with atypical onset as clinical amnestic Mild Cognitive Impairment converted to Alzheimer's disease7-lug-2020Carecchio, M.; Fenoglio, C.; De Riz, M.; Guidi, I.; Comi, C.; Cortini, F.; Venturelli, E.; Restelli, I.; Cantoni, C.; Bresolin, N.; Monaco, F.; Scarpini, E.; Galimberti, D.
Defective Fas-mediated T-cell apoptosis predicts acute onset CIDP7-lug-2020Comi, C.; Osio, M.; Ferretti, M.; Mesturini, R.; Cappellano, G.; Chiocchetti, A.; Carecchio, M.; Nascimbene, C.; Varrasi, C.; Cantello, R.; Mariani, C.; Monaco, F.; Dianzani, U.
Osteopontin is increased in the cerebrospinal fluid of patients with Alzheimer's disease and its levels correlate with cognitive decline7-lug-2020Comi, C.; Carecchio, M.; Chiocchetti, A.; Nicola, S.; Galimberti, D.; Fenoglio, C.; Cappellano, G.; Monaco, F.; Scarpini, E.; Dianzani, U.
C2orf37 mutational spectrum in Woodhouse-Sakati syndrome patients7-lug-2020Alazami, A. M.; Schneider, S. A.; Bonneau, D.; Pasquier, L.; Carecchio, M.; Kojovic, M.; Steindl, K.; De Kerdanet, M.; Nezarati, M. M.; Bhatia, K. P.; Degos, B.; Goh, E.; Alkuraya, F. S.
Atypical Parkinsonism with apraxia and supranuclear gaze abnormalities in type 1 Gaucher disease. Expanding the spectrum: Case report and literature review7-lug-2020Alonso-Canovas, A.; Katschnig, P.; Tucci, A.; Carecchio, M.; Wood, N. W.; Edwards, M.; Martinez Castrillo, J. C.; Burke, D.; Heales, S.; Bhatia, K. P.
Levodopa-induced belly dancer's dyskinesias in Parkinson's disease: Report of one case7-lug-2020Carecchio, M.; Collini, A.; Comi, C.; Cantello, R.; Bhatia, K. P.; Monaco, F.
Phenotypic heterogeneity of the GRN Asp22fs mutation in a large italian kindred7-lug-2020Pietroboni, A. M.; Fumagalli, G. G.; Ghezzi, L.; Fenoglio, C.; Cortini, F.; Serpente, M.; Cantoni, C.; Rotondo, E.; Corti, P.; Carecchio, M.; Bassi, M.; Bresolin, N.; Galbiati, D.; Galimberti, D.; Scarpini, E.
The role of osteopontin in neurodegenerative diseases7-lug-2020Carecchio, M.; Comi, C.
Movement disorders in adult surviving patients with maple syrup urine disease7-lug-2020Carecchio, M.; Schneider, S. A.; Chan, H.; Lachmann, R.; Lee, P. J.; Murphy, E.; Bhatia, K. P.
Cerebrospinal fluid biomarkers in progranulin mutations carriers7-lug-2020Carecchio, M.; Fenoglio, C.; Cortini, F.; Comi, C.; Benussi, L.; Ghidoni, R.; Borroni, B.; De Riz, M.; Serpente, M.; Cantoni, C.; Franceschi, M.; Albertini, V.; Monaco, F.; Rainero, I.; Binetti, G.; Padovani, A.; Bresolin, N.; Scarpini, E.; Galimberti, D.
Teaching NeuroImages: Progressive asymmetric parkinsonism and tendon xanthomas7-lug-2020Kirmi, O.; Murphy, E.; Carecchio, M.; Sulkin, T.; Rankin, J.; Robertson, F.
Movement disorders in adult patients with classical galactosemia7-lug-2020Rubio-Agusti, I.; Carecchio, M.; Bhatia, K. P.; Kojovic, M.; Parees, I.; Chandrashekar, H. S.; Footitt, E. J.; Burke, D.; Edwards, M. J.; Lachmann, R. H. L.; Murphy, E.
The syndrome of deafness-dystonia: Clinical and genetic heterogeneity7-lug-2020Kojovic, M.; Parees, I.; Lampreia, T.; Pienczk-Reclawowicz, K.; Xiromerisiou, G.; Rubio-Agusti, I.; Kramberger, M.; Carecchio, M.; Alazami, A. M.; Brancati, F.; Slawek, J.; Pirtosek, Z.; Valente, E. M.; Alkuraya, F. S.; Edwards, M. J.; Bhatia, K. P.
Defining the epsilon-sarcoglycan (SGCE) gene phenotypic signature in myoclonus-dystonia: A reappraisal of genetic testing criteria7-lug-2020Carecchio, M.; Magliozzi, M.; Copetti, M.; Ferraris, A.; Bernardini, L.; Bonetti, M.; Defazio, G.; Edwards, M. J.; Torrente, I.; Pellegrini, F.; Comi, C.; Bhatia, K. P.; Valente, E. M.
Immunity and inflammation in neurodegenerative diseases7-lug-2020Cappellano, Giuseppe; Carecchio, Miryam; Fleetwood, Thomas; Magistrelli, Luca; Cantello, Roberto; Dianzani, Umberto; Comi, Cristoforo
Evidence of pre-synaptic dopaminergic deficit in a patient with a novel progranulin mutation presenting with atypical parkinsonism7-lug-2020Carecchio, M.; Galimberti, D.; Fenoglio, C.; Serpente, M.; Scarpini, E.; Comi, C.; Terazzi, E.; Cantello, R.
Revisiting the molecular mechanism of neurological manifestations in antiphospholipid syndrome: Beyond vascular damage7-lug-2020Carecchio, M.; Cantello, R.; Comi, C.
Predicting cognitive decline in Parkinson's disease: Can we ask the genes?7-lug-2020de Marchi, F.; Carecchio, M.; Cantello, R.; Comi, C.
Early onset frontotemporal dementia with psychiatric presentation due to the C9ORF72 hexanucleotide repeat expansion: A case report7-lug-2020Gramaglia, C.; Cantello, R.; Terazzi, E.; Carecchio, M.; D'Alfonso, S.; Chieppa, N.; Ressico, F.; Rizza, M. R.; Zeppegno, P.
Prodotti della tipologia (ordinati per Data di deposito in Decrescente ordine): 1 a 20 di 125634
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