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  1. No Access

    Article

    The parkin gene and its phenotype

    Mutations of the parkin gene on chromosome 6 cause autosomal recessive, early onset parkinsonism. This is the most frequent form of monogenic parkinsonism so far identified. The associated phenotypical spectrum ...

    V. Bonifati, G. De Michele, C. B. Lücking, A. Dürr, E. Fabrizio… in Neurological Sciences (2001)

  2. No Access

    Article

    Cognitive improvement during Tolcapone treatment in Parkinson's disease

    The aim of this study was to evaluate the effects of Tolcapone, a reversible, selective inhibitor of catechol-O-methyltransferase, on the cognitive functions of eight patients with advanced Parkinson's disease...

    M. Gasparini, E. Fabrizio, V. Bonifati, G. Meco in Journal of Neural Transmission (1997)

  3. Article

    Fourth meeting of the European Neurological Society 25–29 June 1994 Barcelona, Spain

    L. Harms, A. Bock, W. JÄnisch, J. Valdueza, J. Weber, I. Link… in Journal of Neurology (1994)

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  4. No Access

    Article

    Hallucinations in parkinson disease: Neuropsychological study

    Hallucinations occur fairly frequently in the course of the pharmacological treatment of Parkinson disease. Our aim in this study was to assess first the relation between hallucinations and mental deterioratio...

    Dr. G. Meco, V. Bonifati, G. Cusimano… in The Italian Journal of Neurological Scienc… (1990)