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Frontiers in Aging Neuroscience|June 27, 2022
C9orf72-Related Neurodegenerative Diseases: From Clinical Diagnosis to Therapeutic StrategiesStefania Zampatti, Cristina Peconi, Rosa Campopiano, et al.
Frontiers in Immunology|May 31, 2019
ccf-mtDNA as a Potential Link Between the Brain and Immune System in Neuro-Immunological DisordersStefano Gambardella, Fiona Limanaqi, Rosangela Ferese, et al.
Neuro-Degenerative Diseases|October 3, 2019
Unusual Segregation of APP Mutations in Monogenic Alzheimer DiseaseGioia Mastromoro, Stefano Gambardella, Enrica Marchionni, et al.
The Journal of Biological Chemistry|April 15, 2023
Functional analysis of a conserved site mutation in the DNA end processing enzyme PNKP leading to ataxia with oculomotor apraxia type 4 in humansAzharul Islam, Anirban Chakraborty, Stefano Gambardella, et al.
Archives Italiennes De Biologie|February 7, 2018
Next Generation Sequencing and ALS: known genes, different phenotyphesRosa Campopiano, Larisa Ryskalin, Emiliano Giardina, et al.
Frontiers in Cellular Neuroscience|May 2, 2017
The Monoamine Brainstem Reticular Formation as a Paradigm for Re-Defining Various Phenotypes of Parkinson's Disease Owing Genetic and Anatomical SpecificityStefano Gambardella, Rosangela Ferese, Francesca Biagioni, et al.
Genes|July 28, 2026
Expanding the Clinical and Mutational Spectrum of FBXO7-Related Parkinsonism: A Novel Italian Family and Comprehensive Literature ReviewStefania Zampatti, Claudia Strafella, Rosa Campopiano, et al.
Journal of Molecular Neuroscience : MN|May 22, 2016
A New Splicing Mutation in the L1CAM Gene Responsible for X-Linked Hydrocephalus (HSAS)Rosangela Ferese, Stefania Zampatti, Anna Maria Pia Griguoli, et al.
Frontiers in Neurology|February 4, 2020
A Novel Homozygous Variant in the Fork-Head-Associated Domain of Polynucleotide Kinase Phosphatase in a Patient Affected by Late-Onset Ataxia With Oculomotor Apraxia Type 4Rosa Campopiano, Rosangela Ferese, Fabio Buttari, et al.
Parkinson'S Disease|December 5, 2015
Four Copies of SNCA Responsible for Autosomal Dominant Parkinson's Disease in Two Italian SiblingsRosangela Ferese, Nicola Modugno, Rosa Campopiano, et al.
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