Publications by authors named "Lorena Mosca"

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Mitochondrial D-loop methylation levels inversely correlate with disease duration in amyotrophic lateral sclerosis.
Andrea Stoccoro, Adam R Smith, Lorena Mosca, Alessandro Marocchi, Francesca Gerardi

Epigenomics· February 2024

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Author Correction: Clonally expanded CD8 T cells characterize amyotrophic lateral sclerosis-4.
Laura Campisi, Shahab Chizari, Jessica S Y Ho, Anastasia Gromova, Frederick J Arnold, Lorena Mosca

Nature· August 2022

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Two novel variants in the lecithin:cholesterol acyltransferase gene resulted in classic LCAT deficiency.
Margareta Fistrek Prlic, Marijana Coric, Laura Calabresi, Chiara Pavanello, Lorena Mosca

Atheroscler Plus· August 2022

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Clonally expanded CD8 T cells characterize amyotrophic lateral sclerosis-4.
Laura Campisi, Shahab Chizari, Jessica S Y Ho, Anastasia Gromova, Frederick J Arnold, Lorena Mosca

Nature· June 2022

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Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis.
Janel O Johnson, Ruth Chia, Danny E Miller, Rachel Li, Ravindran Kumaran, Lorena Mosca

JAMA Neurol· October 2021

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Clinical Characterization of Atypical Primary Progressive Aphasia in a 3-Year Longitudinal Study: A Case Report.
Stefania Basilico, Andrea Ciricugno, Giorgio Gelosa, Francesca G Magnani, Lorena Mosca

Cogn Behav Neurol· September 2021

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Facilitations and Hurdles of Genetic Testing in Neuromuscular Disorders.
Andrea Barp, Lorena Mosca, Valeria Ada Sansone

Diagnostics (Basel)· April 2021

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Serum naturally occurring anti-TDP-43 auto-antibodies are increased in amyotrophic lateral sclerosis.
Elisa Conti, Gessica Sala, Susanna Diamanti, Marco Casati, Christian Lunetta, Lorena Mosca

Sci Rep· January 2021

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Urinary neopterin, a new marker of the neuroinflammatory status in amyotrophic lateral sclerosis.
Christian Lunetta, Andrea Lizio, Francesca Gerardi, Claudia Tarlarini, Massimo Filippi, Lorena Mosca

J Neurol· December 2020

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C-PK11195 PET-based molecular study of microglia activation in SOD1 amyotrophic lateral sclerosis.
Giacomo Tondo, Leonardo Iaccarino, Chiara Cerami, Giovanna Emilia Vanoli, Luca Presotto, Lorena Mosca

Ann Clin Transl Neurol· September 2020

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Reduced mitochondrial D-loop methylation levels in sporadic amyotrophic lateral sclerosis.
Andrea Stoccoro, Adam R Smith, Lorena Mosca, Alessandro Marocchi, Francesca Gerardi

Clin Epigenetics· September 2020

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Individuals with familial hypercholesterolemia and cardiovascular events have higher circulating Lp(a) levels.
Chiara Pavanello, Carlo Pirazzi, Kristina Bjorkman, Joakim Sandstedt, Claudia Tarlarini, Lorena Mosca

J Clin Lipidol· July 2020

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Burden of Rare Variants in ALS and Axonal Hereditary Neuropathy Genes Influence Survival in ALS: Insights from a Next Generation Sequencing Study of an Italian ALS Cohort.
Stefania Scarlino, Teuta Domi, Laura Pozzi, Alessandro Romano, Giovanni Battista Pipitone, Lorena Mosca

Int J Mol Sci· May 2020

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Neurofilament light chain and C reactive protein explored as predictors of survival in amyotrophic lateral sclerosis.
Maxim De Schaepdryver, Christian Lunetta, Claudia Tarlarini, Lorena Mosca, Adriano Chio

J Neurol Neurosurg Psychiatry· April 2020

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Identification of a novel NOTCH3 mutation in an Italian family affected by a mild form of CADASIL.
Enrico Ferrante, Lorena Mosca, Cristina Erminio, Silvana Penco, Ugo Cavallari

Neurol Sci· August 2019

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The role of clinical and neuroimaging features in the diagnosis of CADASIL.
Anna Bersano, Gloria Bedini, Hugh Stephen Markus, Paolo Vitali, Enrico Colli-Tibaldi, Lorena Mosca

J Neurol· December 2018

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Mitochondrial DNA copy number and D-loop region methylation in carriers of amyotrophic lateral sclerosis gene mutations.
Andrea Stoccoro, Lorena Mosca, Vittoria Carnicelli, Ugo Cavallari, Christian Lunetta

Epigenomics· November 2018

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ATXN1 intermediate-length polyglutamine expansions are associated with amyotrophic lateral sclerosis.
Serena Lattante, Maria Grazia Pomponi, Amelia Conte, Giuseppe Marangi, Giulia Bisogni, Lorena Mosca

Neurobiol Aging· April 2018

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Increase in DNA methylation in patients with amyotrophic lateral sclerosis carriers of not fully penetrant SOD1 mutations.
Fabio Coppedè, Andrea Stoccoro, Lorena Mosca, Roberta Gallo, Claudia Tarlarini

Amyotroph Lateral Scler Frontotemporal Degener· February 2018

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mutations in Italian patients with amyotrophic lateral sclerosis: genetic and functional characterisation.
Laura Pozzi, Fabiola Valenza, Lorena Mosca, Andrea Dal Mas, Teuta Domi

J Neurol Neurosurg Psychiatry· October 2017

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Clinical Pregenetic Screening for Stroke Monogenic Diseases: Results From Lombardia GENS Registry.
Anna Bersano, Hugh Stephen Markus, Silvana Quaglini, Eloisa Arbustini, Silvia Lanfranconi, Lorena Mosca

Stroke· July 2016

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Hypomorphic NOTCH3 mutation in an Italian family with CADASIL features.
Marcello Moccia, Lorena Mosca, Roberto Erro, Mariarosaria Cervasio, Roberto Allocca

Neurobiol Aging· January 2015

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Mutational screening of NOTCH3 gene reveals two novel mutations: complexity of CADASIL diagnosis.
Lorena Mosca, Francesca Rivieri, Raffaella Tanel, Aldo Bonfante, Alessandro Burlina

J Mol Neurosci· December 2014

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Progressive parkinsonism, balance difficulties, and supranuclear gaze palsy.
Roberto Erro, Andrew J Lees, Marcello Moccia, Marina Picillo, Silvana Penco, Lorena Mosca

JAMA Neurol· January 2014

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De novo MGC4607 gene heterozygous missense variants in a child with multiple cerebral cavernous malformations.
Lorena Mosca, Silvana Pileggi, Francesca Avemaria, Claudia Tarlarini, Maria Sole Cigoli

J Mol Neurosci· July 2012

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