Publications by authors named "Francesca Cortini"

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The LUNET Project: Developing the Italian Systemic Erythematous Lupus Network.
Ilaria Mormile, Luisa Brussino, Giorgio Walter Canonica, Francesca Cortini, Maria Teresa Costantino

J Clin Med· September 2025

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PICALM Gene Methylation in Blood of Alzheimer's Disease Patients Is Associated with Cognitive Decline.
Roberta Mercorio, Laura Pergoli, Daniela Galimberti, Chiara Favero, Michele Carugno, Francesca Cortini

J Alzheimers Dis· July 2019

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Understanding the basis of Ehlers-Danlos syndrome in the era of the next-generation sequencing.
Francesca Cortini, Chiara Villa, Barbara Marinelli, Romina Combi, Angela Cecilia Pesatori

Arch Dermatol Res· May 2019

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Emerging roles of long non-coding RNAs in the pathogenesis of Alzheimer's disease.
Francesca Cortini, Francesca Roma, Chiara Villa

Ageing Res Rev· March 2019

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Epileptic seizures in autosomal dominant forms of Alzheimer's disease.
Francesca Cortini, Claudia Cantoni, Chiara Villa

Seizure· October 2018

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A Rare Cause of Juvenile Stroke: Extracranial Carotid Artery Aneurysm with Venous Complete Reconstruction of the Carotid Bifurcation.
Maurizio Domanin, Silvia Lanfranconi, Silvia Romagnoli, Letterio Runza, Francesca Cortini

Pediatr Neurosurg· September 2018

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RETRACTED: Ehlers-Danlos syndrome caused by the c.934C>T, p. Arg312Cys mutation in COL1A1 gene: an Italian family without cardiovascular events.
Francesca Cortini, Barbara Marinelli, Manuela Seia, Agostino Seresini, Alessandra Bassotti

Dermatol Online J· September 2018

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Ehlers-Danlos syndrome caused by the c.934C>T, p. Arg312Cys mutation in COL1A1 gene: an Italian family without cardiovascular events.
Francesca Cortini, Barbara Marinelli, Manuela Seia, Agostino Seresini, Alessandra Bassotti

Dermatol Online J· July 2018

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Ehlers-Danlos syndromes and epilepsy: An updated review.
Francesca Cortini, Chiara Villa

Seizure· April 2018

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A New COL3A1 Mutation in Ehlers-Danlos Syndrome Vascular Type With Different Phenotypes in the Same Family.
Francesca Cortini, Barbara Marinelli, Silvia Romi, Agostino Seresini, Angela Cecilia Pesatori

Vasc Endovascular Surg· April 2017

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Next-generation sequencing and a novel COL3A1 mutation associated with vascular Ehlers-Danlos syndrome with severe intestinal involvement: a case report.
Francesca Cortini, Barbara Marinelli, Manuela Seia, Barbara De Giorgio, Angela Cecilia Pesatori

J Med Case Rep· October 2016

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Effects of particulate matter exposure on multiple sclerosis hospital admission in Lombardy region, Italy.
Laura Angelici, Mirko Piola, Tommaso Cavalleri, Giorgia Randi, Francesca Cortini

Environ Res· February 2016

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Progranulin gene variability and plasma levels in bipolar disorder and schizophrenia.
Daniela Galimberti, Bernardo Dell'Osso, Chiara Fenoglio, Chiara Villa, Francesca Cortini

PLoS One· October 2012

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Selective DNA methylation of BDNF promoter in bipolar disorder: differences among patients with BDI and BDII.
Claudio D'Addario, Bernardo Dell'Osso, Maria Carlotta Palazzo, Beatrice Benatti, Licia Lietti, Francesca Cortini

Neuropsychopharmacology· June 2012

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Cerebrospinal fluid biomarkers in Progranulin mutations carriers.
Miryam Carecchio, Chiara Fenoglio, Francesca Cortini, Cristoforo Comi, Luisa Benussi

J Alzheimers Dis· April 2012

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BAG1 is a protective factor for sporadic frontotemporal lobar degeneration but not for Alzheimer's disease.
Eliana Venturelli, Chiara Villa, Chiara Fenoglio, Francesca Clerici, Alessandra Marcone, Francesca Cortini

J Alzheimers Dis· March 2012

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A novel MAPT mutation associated with the clinical phenotype of progressive nonfluent aphasia.
Chiara Villa, Laura Ghezzi, Anna M Pietroboni, Chiara Fenoglio, Francesca Cortini

J Alzheimers Dis· January 2012

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Role of OLR1 and its regulating hsa-miR369-3p in Alzheimer's disease: genetics and expression analysis.
Maria Serpente, Chiara Fenoglio, Chiara Villa, Francesca Cortini, Claudia Cantoni

J Alzheimers Dis· January 2012

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Expression and genetic analysis of miRNAs involved in CD4+ cell activation in patients with multiple sclerosis.
Chiara Fenoglio, Claudia Cantoni, Milena De Riz, Elisa Ridolfi, Francesca Cortini

Neurosci Lett· October 2011

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Phenotypic heterogeneity of the GRN Asp22fs mutation in a large Italian kindred.
Anna M Pietroboni, Giorgio G Fumagalli, Laura Ghezzi, Chiara Fenoglio, Francesca Cortini

J Alzheimers Dis· August 2011

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GSK3β genetic variability in patients with Multiple Sclerosis.
Daniela Galimberti, James Macmurray, Diego Scalabrini, Chiara Fenoglio, Milena De Riz, Francesca Cortini

Neurosci Lett· June 2011

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Role of hnRNP-A1 and miR-590-3p in neuronal death: genetics and expression analysis in patients with Alzheimer disease and frontotemporal lobar degeneration.
Chiara Villa, Chiara Fenoglio, Milena De Riz, Francesca Clerici, Alessandra Marcone, Francesca Cortini

Rejuvenation Res· June 2011

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Cell-dependent kinase inhibitor 2A and 2B genetic variability in patients with Alzheimer's disease.
Francesca Cortini, Chiara Fenoglio, Eliana Venturelli, Chiara Villa, Francesca Clerici

J Neurol· April 2011

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Is KIF24 a genetic risk factor for Frontotemporal Lobar Degeneration?
Eliana Venturelli, Chiara Villa, Chiara Fenoglio, Francesca Clerici, Alessandra Marcone, Francesca Cortini

Neurosci Lett· October 2010

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GRN variability contributes to sporadic frontotemporal lobar degeneration.
Daniela Galimberti, Chiara Fenoglio, Francesca Cortini, Maria Serpente, Eliana Venturelli

J Alzheimers Dis· August 2010

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