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Enza Maria Valente

Researcher at University of Pavia

Publications -  338
Citations -  27726

Enza Maria Valente is an academic researcher from University of Pavia. The author has contributed to research in topics: Joubert syndrome & Medicine. The author has an hindex of 67, co-authored 302 publications receiving 24057 citations. Previous affiliations of Enza Maria Valente include University of California & University College London.

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Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)

Daniel J. Klionsky, +2522 more
- 21 Jan 2016 - 
TL;DR: In this paper, the authors present a set of guidelines for the selection and interpretation of methods for use by investigators who aim to examine macro-autophagy and related processes, as well as for reviewers who need to provide realistic and reasonable critiques of papers that are focused on these processes.
Journal ArticleDOI

Guidelines for the use and interpretation of assays for monitoring autophagy

Daniel J. Klionsky, +1287 more
- 01 Apr 2012 - 
TL;DR: These guidelines are presented for the selection and interpretation of methods for use by investigators who aim to examine macroautophagy and related processes, as well as for reviewers who need to provide realistic and reasonable critiques of papers that are focused on these processes.
Journal ArticleDOI

An SCN9A channelopathy causes congenital inability to experience pain

James J. Cox, +18 more
- 14 Dec 2006 - 
TL;DR: The data suggest that SCN9A is an essential and non-redundant requirement for nociception in humans, and should stimulate the search for novel analgesics that selectively target this sodium channel subunit.
Journal ArticleDOI

PINK1 mutations are associated with sporadic early-onset parkinsonism.

Enza Maria Valente, +9 more
- 01 Sep 2004 - 
TL;DR: The hypothesis that haploinsufficiency of PINK1, as well as of other EOP genes, may represent a susceptibility factor toward parkinsonism is supported, however, the pathogenetic significance of heterozygous Pink1 mutations still remains to be clarified.
Journal ArticleDOI

Localization of a novel locus for autosomal recessive early-onset parkinsonism, PARK6, on human chromosome 1p35-p36

Enza Maria Valente, +7 more
- 01 Apr 2001 - 
TL;DR: A large Sicilian family with four definitely affected members (the Marsala kindred) was identified, characterized by early-onset parkinsonism, with slow progression and sustained response to levodopa, and the Parkin-associated phenotype is broad, and some cases are indistinguishable from idiopathic PD.