Author pages are created from data sourced from our academic publisher partnerships and public sources.
- Publications
- Influence
Diffusion tensor imaging in patients with primary cervical dystonia and in patients with blepharospasm
- G. Fabbrini, P. Pantano, +5 authors A. Berardelli
- Medicine
- European journal of neurology
- 1 February 2008
Diffusion tensor imaging (DTI) analyses the movement of water molecules within the cerebral white matter thus providing information on ultrastructural brain changes. We studied 18 patients with… Expand
Psychiatric disorders in adult‐onset focal dystonia: A case‐control study
- G. Fabbrini, I. Berardelli, +5 authors A. Berardelli
- Psychology, Medicine
- Movement disorders : official journal of the…
- 15 March 2010
In a single‐center, case–control study, we investigated the frequency and types of psychiatric disturbances in 89 consecutive patients with various primary focal dystonias (34 had cervical dystonia… Expand
ATP13A2 missense mutations in juvenile parkinsonism and young onset Parkinson disease
- A. Di Fonzo, H. Chien, +22 authors V. Bonifati
- Medicine, Psychology
- Neurology
- 8 May 2007
Objective: To assess the prevalence, nature, and associated phenotypes of ATP13A2 gene mutations among patients with juvenile parkinsonism (onset <21 years) or young onset (between 21 and 40 years)… Expand
Abnormal Salivary Total and Oligomeric Alpha-Synuclein in Parkinson’s Disease
- G. Vivacqua, A. Latorre, +7 authors A. Berardelli
- Medicine
- PloS one
- 24 March 2016
In Parkinson’s disease (PD), alpha-synuclein (a-syn) can be detected in biological fluids including saliva. Although previous studies found reduced a-syn total (a-syntotal) concentration in saliva of… Expand
Early-onset parkinsonism associated with PINK1 mutations
- V. Bonifati, C. Rohé, +32 authors B. Oostra
- Medicine
- Neurology
- 12 July 2005
Objective: To assess the prevalence, nature, and associated phenotypes of PINK1 gene mutations in a large series of patients with early-onset (<50 years) parkinsonism. Methods: The authors studied… Expand
Levodopa‐induced dyskinesias
- G. Fabbrini, J. Brotchie, F. Grandas, M. Nomoto, C. Götz
- Medicine
- Movement disorders : official journal of the…
- 30 July 2007
Levodopa‐induced dyskinesias (LID) are common and difficult to treat. This review focuses on three issues related to LID: clinical features, classification and rating, pathophysiology and… Expand
Prevalence and clinical features of hedonistic homeostatic dysregulation in Parkinson's disease
- Francesca Romana Pezzella, C. Colosimo, +4 authors G. Meco
- Medicine
- Movement disorders : official journal of the…
- 1 January 2005
Hedonistic homeostatic dysregulation (HHD) is a neuropsychiatric disorder recently described in Parkinson's disease (PD), which is characterized by self‐medication and addiction to dopaminergic… Expand
Increased expression of dopamine receptors on lymphocytes in Parkinson's disease
- P. Barbanti, G. Fabbrini, +9 authors G. Lenzi
- Medicine
- Movement disorders : official journal of the…
- 1 September 1999
Dopamine D1‐like and D2‐like receptors on peripheral blood lymphocytes (PBL) were assayed in 50 de novo patients with idiopathic Parkinson's disease (PD), in 36 neurologic control subjects… Expand
Donepezil in the treatment of hallucinations and delusions in Parkinson’s disease
- G. Fabbrini, P. Barbanti, C. Aurilia, C. Pauletti, G. Lenzi, G. Meco
- Psychology, Medicine
- Neurological Sciences
- 1 April 2002
As cholinergic mechanisms may be at least partially responsible for hallucinations and delusions in Parkinson’s disease (PD), we conducted an open study in 8 PD patients to assess the efficacy and… Expand
A study of five candidate genes in Parkinson's disease and related neurodegenerative disorders. European Study Group on Atypical Parkinsonism.
- D. Nicholl, P. Bennett, +12 authors A. Williams
- Medicine
- Neurology
- 22 October 1999
OBJECTIVE
To determine whether reported genetic association of polymorphisms in the CYP2D6, CYP1A1, N-acetyltransferase 2 (NAT2), DAT1, and glutathione s-transferase M1 (GSTM1) genes with PD were… Expand