Nicola Rizzuto

Affiliations: 
University of Verona, Verona, WI, United States 
Website:
http://www.medicina.univr.it/fol/main?ent=persona&id=1076&lang=it
Google:
"Nicola Rizzuto"
Bio:

http://www.medicina.univr.it/documenti/Persona/curr/curr728917.pdf

Mean distance: 16.42 (cluster 24)
 
SNBCP
Cross-listing: Neuropathology Tree

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Publications

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Piscosquito G, Reilly MM, Schenone A, et al. (2014) Is overwork weakness relevant in Charcot-Marie-Tooth disease? Journal of Neurology, Neurosurgery, and Psychiatry. 85: 1354-8
Pareyson D, Reilly MM, Schenone A, et al. (2011) Ascorbic acid in charcot-marie-tooth disease type 1A (CMTTRIAAL and CMT-TRAUK): A double-blind randomised trial The Lancet Neurology. 10: 320-328
Iemolo F, Cavallaro T, Rizzuto N. (2010) Atypical Alzheimer's disease: a case report. Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 31: 643-6
Boaretto F, Vettori A, Casarin A, et al. (2010) Severe CMT type 2 with fatal encephalopathy associated with a novel MFN2 splicing mutation. Neurology. 74: 1919-21
Padua L, Pareyson D, Aprile I, et al. (2010) Natural history of Charcot-Marie-Tooth 2: 2-year follow-up of muscle strength, walking ability and quality of life. Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 31: 175-8
Zanusso G, Ferrari S, Benedetti D, et al. (2009) Different prion conformers target the olfactory pathway in sporadic Creutzfeldt-Jakob disease. Annals of the New York Academy of Sciences. 1170: 637-43
Mazzucco S, Anzola GP, Rizzuto N. (2009) Methodological issues in right-to-left shunt detection in CADASIL patients. Stroke; a Journal of Cerebral Circulation. 40: e509; author reply e
Fabrizi GM, Taioli F, Cavallaro T, et al. (2009) Further evidence that mutations in FGD4/frabin cause Charcot-Marie-Tooth disease type 4H. Neurology. 72: 1160-4
Rosati A, Marconi S, Pollo B, et al. (2009) Epilepsy in glioblastoma multiforme: correlation with glutamine synthetase levels. Journal of Neuro-Oncology. 93: 319-24
Mazzucco S, Anzola GP, Ferrarini M, et al. (2009) Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy and right-to-left shunt: lack of evidence for an association in a prevalence study. European Neurology. 61: 46-9
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