Filippo Arrigoni - Dissemin

Papers authored by Filippo Arrigoni

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2016 Eleonora Maggioni, Claudio Zucca, Gianluigi Reni

, Sergio Cerutti, Fabio M. Triulzi, Anna M. Bianchi, Filippo Arrigoni

Investigation of the electrophysiological correlates of negative BOLD response during intermittent photic stimulation: An EEG-fMRI study

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Denis Peruzzo

, Filippo Arrigoni

, Fabio Triulzi, Andrea Righini

, Cecilia Parazzini, Umberto Castellani

A framework for the automatic detection and characterization of brain malformations: Validation on the corpus callosum

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2015 Chiara Gagliardi

, Viola Brenna, Romina Romaniello, Filippo Arrigoni

, Alessandro Tavano, Marta Romani, Enza Maria Valente, Renato Borgatti

Cognitive rehabilitation in a child with Joubert Syndrome: Developmental trends and adaptive changes in a single case report

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Filippo Arrigoni

, Romina Romaniello, Denis Peruzzo

, Andrea Righini, Cecilia Parazzini, Paola Colombo, Maria Teresa Bassi, Fabio Triulzi, Renato Borgatti

Aberrant supracallosal longitudinal bundle: MR features, pathogenesis and associated clinical phenotype

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Filippo Arrigoni

, Romina Romaniello, Andrea Nordio, Chiara Gagliardi, Renato Borgatti

Learning to live without the cerebellum:

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Romina Romaniello, Francesco Saettini

, Elena Panzeri, Filippo Arrigoni

, Maria T. Bassi, Renato Borgatti

A de-novo STXBP1 gene mutation in a patient showing the Rett syndrome phenotype:

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Eleonora Maggioni, Erika Molteni, Claudio Zucca, Gianluigi Reni

, Sergio Cerutti, Fabio M. Triulzi, Filippo Arrigoni

, Anna M. Bianchi

Investigation of negative BOLD responses in human brain through NIRS technique. A visual stimulation study

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Sandra Strazzer, Maria A. Rocca, ErikaMolteni, Erika Molteni, Ermelinda De Meo, Ermelinda DeMeo, Monica Recla, Paola Valsasina

, Filippo Arrigoni

, Susanna Galbiati, Alessandra Bardoni, Massimo Filippi

Altered Recruitment of the Attention Network Is Associated with Disability and Cognitive Impairment in Pediatric Patients with Acquired Brain Injury

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2014 Chiara Vantaggiato

, Orazio Cantoni, Andrea Guidarelli, Romina Romaniello, Andrea Citterio, Filippo Arrigoni

, Chiara Doneda, Marianna Castelli, Giovanni Airoldi, Nereo Bresolin, Renato Borgatti, Maria Teresa Bassi

Novel SETX variants in a patient with ataxia, neuropathy, and oculomotor apraxia are associated with normal sensitivity to oxidative DNA damaging agents

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This paper is available in a repository.

Romina Romaniello, Filippo Arrigoni

, Maria Teresa Bassi, Renato Borgatti

Mutations in α- and β-tubulin encoding genes: Implications in brain malformations

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Eleonora Maggioni, Maria Gabriella Tana, Filippo Arrigoni

, Claudio Zucca, Anna Maria Bianchi

Constructing fMRI connectivity networks: A whole brain functional parcellation method for node definition

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Denis Peruzzo

, Filippo Arrigoni

, Fabio Triulzi, Cecilia Parazzini, Umberto Castellani

Detection of Corpus Callosum Malformations in Pediatric Population Using the Discriminative Direction in Multiple Kernel Learning

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2013 Andrea Citterio, Alessia Arnoldi, Elena Panzeri, Maria Grazia D'Angelo, Maria Grazia D’Angelo, Massimiliano Filosto, Robertino Dilena, Filippo Arrigoni

, Marianna Castelli, Cristina Maghini, Chiara Germiniasi, Francesca Menni, Andrea Martinuzzi

, Nereo Bresolin, Maria Teresa Bassi

Mutations in CYP2U1, DDHD2 and GBA2 genes are rare causes of complicated forms of hereditary spastic paraparesis

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E. Maggioni, E. Molteni, F. Arrigoni

, C. Zucca, G. Reni

, F. M. Triulzi, A. M. Bianchi

Coupling of fMRI and NIRS measurements in the study of negative BOLD response to intermittent photic stimulation

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Erika Molteni, Filippo Arrigoni

, Alessandra Bardoni, Sara Galbiati, Federica Villa, Katia Colombo, Sandra Strazzer

Bedside assessment of residual functional activation in minimally conscious state using NIRS and general linear models

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2012 Romina Romaniello, Filippo Arrigoni

, Andrea Citterio, Alessandra Tonelli, Cinzia Sforzini, Carmelo Rizzari

, Marco Pessina, Fabio Triulzi, Maria Teresa Bassi, Renato Borgatti

Cerebroretinal Microangiopathy With Calcifications and Cysts Associated With CTC1 and NDP Mutations

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Romina Romaniello, Alessandra Tonelli, Filippo Arrigoni

, Cinzia Baschirotto, Fabio Triulzi, Nereo Bresolin, Maria Teresa Bassi, Renato Borgatti

A novel mutation in the β‐tubulin gene TUBB2B associated with complex malformation of cortical development and deficits in axonal guidance

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This paper was not found in any repository; the policy of its publisher is unknown or unclear.

Andrea Righini, Cecilia Parazzini, Chiara Doneda, Laura Avagliano, Filippo Arrigoni

, Mariangela Rustico, Dario Consonni

, Thomas Joseph Re, Re Tj, Gaetano Bulfamante, Fabio Triulzi

Early formative stage of human focal cortical gyration anomalies: fetal MRI.

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Andrea Poretti, Giuseppina Vitiello

, Raoul Cm M. Hennekam, Filippo Arrigoni

, Enrico Bertini, Renato Borgatti, Francesco Brancati, Stefano D'Arrigo, Francesca Faravelli, Lucio Giordano, Thierry Agm G. M. Huisman, Miriam Iannicelli, Gerhard Kluger, Marten Kyllerman, Magnus Landgren and 9 other authors

Delineation and diagnostic criteria of Oral-Facial-Digital Syndrome type VI

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Cecilia Parazzini, Andrea Righini, Chiara Doneda, Filippo Arrigoni

, Mariangela Rustico, Mariano Lanna, Fabio Triulzi

Is fetal magnetic resonance imaging indicated when ultrasound isolated mild ventriculomegaly is present in pregnancies with no risk factors?

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Papers authored by Filippo Arrigoni