Publications by authors named "Irene Colombo"

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Susceptibility to brain ischemia and the association between migraine and spontaneous cervical artery dissection.
Elisabetta Del Zotto, Mario Grassi, Marialuisa Zedde, Andrea Zini, Anna Bersano, Irene Colombo

J Neurol· November 2023

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Sex differences in ischemic stroke during COVID-19 first outbreak in northern Italy.
Davide Sangalli, Maurizio Versino, Irene Colombo, Alfonso Ciccone, Simone Beretta, Antonio Colombo

J Neurol Sci· November 2023

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Risk Profile of Patients with Spontaneous Cervical Artery Dissection.
Elisabetta Del Zotto, Mario Grassi, Marialuisa Zedde, Andrea Zini, Anna Bersano, Irene Colombo

Ann Neurol· September 2023

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Antithrombotic therapy in the postacute phase of cervical artery dissection: the Italian Project on Stroke in Young Adults Cervical Artery Dissection.
Debora Pezzini, Mario Grassi, Maria Luisa Zedde, Andrea Zini, Anna Bersano, Irene Colombo

J Neurol Neurosurg Psychiatry· July 2022

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Impact of SARS-CoV-2 infection on acute intracerebral haemorrhage in northern Italy.
Davide Sangalli, Filippo Martinelli-Boneschi, Maurizio Versino, Irene Colombo, Alfonso Ciccone, Antonio Colombo

J Neurol Sci· July 2021

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Clinical Features of Patients With Cervical Artery Dissection and Fibromuscular Dysplasia.
Sonia Bonacina, Mario Grassi, Marialuisa Zedde, Andrea Zini, Anna Bersano, Irene Colombo

Stroke· March 2021

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Limb girdle muscular dystrophy due to gene mutations: new mutations expand the clinical spectrum of a still challenging diagnosis.
Francesca Magri, Roberta Brusa, Luca Bello, Lorenzo Peverelli, Roberto Del Bo, Irene Colombo

Acta Myol· June 2020

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The clinical spectrum of -related myopathy.
Claudio Semplicini, Cinzia Bertolin, Luca Bello, Boris Pantic, Francesca Guidolin, Irene Colombo

Neurology· October 2018

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Exertional rhabdomyolysis leading to acute kidney injury: when genetic defects are diagnosed in adult life.
David Cucchiari, Irene Colombo, Ottavia Amato, Manuel Alfredo Podestà, Francesco Reggiani

CEN Case Rep· May 2018

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A case report with the peculiar concomitance of 2 different genetic syndromes.
Alberto Lerario, Irene Colombo, Donatella Milani, Lorenzo Peverelli, Luisa Villa

Medicine (Baltimore)· December 2016

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Coexistence of VHL Disease and CPT2 Deficiency: A Case Report.
Alfonso Massimiliano Ferrara, Monica Sciacco, Stefania Zovato, Silvia Rizzati, Irene Colombo

Cancer Res Treat· October 2016

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Longitudinal follow-up and muscle MRI pattern of two siblings with polyglucosan body myopathy due to glycogenin-1 mutation.
Irene Colombo, Serena Pagliarani, Silvia Testolin, Claudia Maria Cinnante, Gigliola Fagiolari

J Neurol Neurosurg Psychiatry· July 2016

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New Mutations in NEB Gene Discovered by Targeted Next-Generation Sequencing in Nemaline Myopathy Italian Patients.
Daniela Piga, Francesca Magri, Dario Ronchi, Stefania Corti, Denise Cassandrini, Irene Colombo

J Mol Neurosci· July 2016

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ISPD mutations account for a small proportion of Italian Limb Girdle Muscular Dystrophy cases.
Francesca Magri, Irene Colombo, Roberto Del Bo, Stefano Previtali, Roberta Brusa

BMC Neurol· September 2015

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Centronuclear myopathies: genotype-phenotype correlation and frequency of defined genetic forms in an Italian cohort.
Fabiana Fattori, Lorenzo Maggi, Claudio Bruno, Denise Cassandrini, Valentina Codemo, Irene Colombo

J Neurol· July 2015

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Impaired Muscle Mitochondrial Biogenesis and Myogenesis in Spinal Muscular Atrophy.
Michela Ripolone, Dario Ronchi, Raffaella Violano, Dionis Vallejo, Gigliola Fagiolari, Irene Colombo

JAMA Neurol· June 2015

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Congenital myopathies: Natural history of a large pediatric cohort.
Irene Colombo, Mariacristina Scoto, Adnan Y Manzur, Stephanie A Robb, Lorenzo Maggi

Neurology· January 2015

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Mitochondrial disease heterogeneity: a prognostic challenge.
Maurizio Moggio, Irene Colombo, Lorenzo Peverelli, Luisa Villa, Rubjona Xhani

Acta Myol· October 2014

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Optic atrophy plus phenotype due to mutations in the OPA1 gene: two more Italian families.
Michela Ranieri, Roberto Del Bo, Andreina Bordoni, Dario Ronchi, Irene Colombo

J Neurol Sci· April 2012

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Two novel mutations in PEO1 (twinkle) gene associated with chronic external ophthalmoplegia.
Dario Ronchi, Elisa Fassone, Andreina Bordoni, Monica Sciacco, Valeria Lucchini, Irene Colombo

J Neurol Sci· September 2011

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Steroid-responsive Hashimoto encephalopathy mimicking Creutzfeldt-Jakob disease.
Domenico Santoro, Irene Colombo, Isabella Ghione, Lorenzo Peverelli, Nereo Bresolin

Neurol Sci· August 2011

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