Le ceroido-lipofuscinosi neuronali

F. Cardona, N. Nardocci, E. Rosati

Research output: Contribution to journalArticle

Abstract

Neuronal Ceroid Lipofuscinosis (NCL) are reviewed. All four main types are progressive encephalopathies characterized by neuronal and extraneuronal accumulation of ceroid and lipofuscin like storage cytosomes. The pathogenesis of NCL is still unknown, in most subtypes. This review concerns recent advances in genetic studies, broadening of the clinical spectrum of NCL and progress in prenatal diagnosis.

Original languageItalian
Pages (from-to)53-58
Number of pages6
JournalGiornale di Neuropsicofarmacologia
Volume19
Issue number3
Publication statusPublished - May 1997

ASJC Scopus subject areas

  • Neuroscience(all)
  • Pharmaceutical Science
  • Pharmacology
  • Neuropsychology and Physiological Psychology

Cite this

Le ceroido-lipofuscinosi neuronali. / Cardona, F.; Nardocci, N.; Rosati, E.

In: Giornale di Neuropsicofarmacologia, Vol. 19, No. 3, 05.1997, p. 53-58.

Research output: Contribution to journalArticle

Cardona, F, Nardocci, N & Rosati, E 1997, 'Le ceroido-lipofuscinosi neuronali', Giornale di Neuropsicofarmacologia, vol. 19, no. 3, pp. 53-58.
Cardona, F. ; Nardocci, N. ; Rosati, E. / Le ceroido-lipofuscinosi neuronali. In: Giornale di Neuropsicofarmacologia. 1997 ; Vol. 19, No. 3. pp. 53-58.
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