Elena Piccoli

Milan, Italy

Last Updated: 09/26/2026

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Found 14 publications

The Role of Zinc in Developed Countries in Pediatric Patients: A 360-Degree View.

The Role of Zinc in Developed Countries in Pediatric Patients: A 360-Degree View.

Journal: Biomolecules

Published: May 14, 2024

Alzheimer neuropathology without frontotemporal lobar degeneration hallmarks (TAR DNA-binding protein 43 inclusions) in missense progranulin mutation Cys139Arg.

Alzheimer neuropathology without frontotemporal lobar degeneration hallmarks (TAR DNA-binding protein 43 inclusions) in missense progranulin mutation Cys139Arg.

Journal: Brain pathology (Zurich, Switzerland)

Published: September 13, 2016

A cluster of progranulin C157KfsX97 mutations in Southern Italy: clinical characterization and genetic correlations.

A cluster of progranulin C157KfsX97 mutations in Southern Italy: clinical characterization and genetic correlations.

Journal: Neurobiology of aging

Published: September 12, 2016

Novel PSEN1 mutations (H214N and R220P) associated with familial Alzheimer's disease identified by targeted exome sequencing.

Novel PSEN1 mutations (H214N and R220P) associated with familial Alzheimer's disease identified by targeted exome sequencing.

Journal: Neurobiology of aging

Published: November 10, 2015

Amiodarone increases positive-strand RNA virus replication in vitro: implications for its use in patients with viral infections.

Amiodarone increases positive-strand RNA virus replication in vitro: implications for its use in patients with viral infections.

Journal: The Journal of antimicrobial chemotherapy

Published: October 03, 2015

Missense mutations in progranulin gene associated with frontotemporal lobar degeneration: study of pathogenetic features.

Missense mutations in progranulin gene associated with frontotemporal lobar degeneration: study of pathogenetic features.

Journal: Neurobiology of aging

Published: May 29, 2015

C9ORF72 hexanucleotide repeat number in frontotemporal lobar degeneration: a genotype-phenotype correlation study.

C9ORF72 hexanucleotide repeat number in frontotemporal lobar degeneration: a genotype-phenotype correlation study.

Journal: Journal of Alzheimer's disease : JAD

Published: March 05, 2015

A case of progressive frontal lobe syndrome in a sporadic form of Cerebral Amyloid Angiopathy: A singular overlap with fronto-temporal dementia?

A case of progressive frontal lobe syndrome in a sporadic form of Cerebral Amyloid Angiopathy: A singular overlap with fronto-temporal dementia?

Journal: Journal of the neurological sciences

Published: December 17, 2014

C9ORF72 hexanucleotide repeat number in frontotemporal lobar degeneration: a genotype-phenotype correlation study.

C9ORF72 hexanucleotide repeat number in frontotemporal lobar degeneration: a genotype-phenotype correlation study.

Journal: Journal of Alzheimer's disease : JAD

Published: September 26, 2013

Different mutations at V363 MAPT codon are associated with atypical clinical phenotypes and show unusual structural and functional features.

Different mutations at V363 MAPT codon are associated with atypical clinical phenotypes and show unusual structural and functional features.

Journal: Neurobiology of aging

Published: June 14, 2013

Mutations in MAPT give rise to aneuploidy in animal models of tauopathy.

Mutations in MAPT give rise to aneuploidy in animal models of tauopathy.

Journal: Neurogenetics

Published: April 09, 2013

In vitro antiviral activity of hypothiocyanite against A/H1N1/2009 pandemic influenza virus.

In vitro antiviral activity of hypothiocyanite against A/H1N1/2009 pandemic influenza virus.

Journal: International journal of hygiene and environmental health

Published: December 13, 2012

Showing 1-12 of 14

Last Updated: 09/26/2026