Lysosomal hydrolases in cerebrospinal fluid from subjects with Parkinson's disease

Recent studies have shown a genetic association between glucocerebrosidase deficiencies and Parkinson's disease (PD). To further explore this issue the activity of β‐glucocerebrosidase and the activities of other lysosomal enzymes, α‐mannosidase, β‐mannosidase, β‐hexosaminidase, and β‐galactosi...

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Veröffentlicht in:	Movement disorders 2007-07, Vol.22 (10), p.1481-1484
Hauptverfasser:	Balducci, Chiara, Pierguidi, Laura, Persichetti, Emanuele, Parnetti, Lucilla, Sbaragli, Michele, Tassi, Carmelo, Orlacchio, Aldo, Calabresi, Paolo, Beccari, Tommaso, Rossi, Aroldo
Format:	Artikel
Sprache:	eng
Schlagworte:	Aged Biological and medical sciences Chromatography, Ion Exchange - methods Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases Female Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy Humans Hyaluronoglucosaminidase - cerebrospinal fluid Male Medical sciences Middle Aged Nervous system (semeiology, syndromes) Neurology Parkinson Disease - cerebrospinal fluid Parkinson's disease Statistics, Nonparametric α-mannosidase β-glucocerebrosidase β-hexosaminidase β-mannosidase
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