Ettore Salsano - Dissemin

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All papers authored by Ettore Salsano

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2024 Chiara Benzoni, Ettore Salsano

ORCID

Dataset related to article: Adult-onset leukodystrophy with vanishing white matter: a case series of 19 patients

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Marco Moscatelli, Chiara Benzoni, Fabio M. Doniselli

ORCID

, Mattia Verri, Riccardo Pascuzzo, Domenico Aquino, Federica Mazzi, Alessandra Erbetta, Ettore Salsano

ORCID

Dataset related to article: Interval between contrast administration and T1-weighted MRI for cerebral adrenoleukodystrophy: a single-case observation

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2023 Ilaria Quartesan, Adolfo López de Munain, Elisa Vegezzi

ORCID

, Riccardo Currò, Amanda Heslegrave, Chiara Pisciotta, Pablo Iruzubieta, Alessandro Salvalaggio, Gorka Fernández‐Eulate, Natalia Dominik, Bianca Rugginini, Arianna Manini, Elena Abati, Stefano Facchini, Katarina Manso and 19 other authors

Serum Neurofilament Light Chain in Replication Factor Complex Subunit 1 CANVAS and Disease Spectrum

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2022 Marc Engelen

ORCID

, Wouter J. C. van Ballegoij

ORCID

, Eric James Mallack

ORCID

, Keith P. Van Haren

ORCID

, Wolfgang Köhler, Ettore Salsano

ORCID

, A. S. P. van Trotsenburg, Fanny Mochel, Caroline Sevin, Molly O. Regelmann, Nicholas A. Tritos, Alyssa Halper, Robin H. Lachmann

ORCID

, James Davison, Gerald V. Raymond and 13 other authors

International Recommendations for the Diagnosis and Management of Patients With Adrenoleukodystrophy

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

Davide Rossi Sebastiano, Daniele Cazzato, Elisa Visani, Eleonora Dalla Bella, Laura Brambilla, Grazia Devigili, Paola Caroppo, Lorenzo Maggi, Lorenzo Nanetti, Ettore Salsano

ORCID

, Laura Canafoglia

ORCID

, Isabella Canavero, Elena Anghileri, Paola Lanteri

Dataset related to article "Significance and clinical suggestions for the Somatosensory Evoked Potentials increased in amplitude revealed by a large sample of neurological patients"

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2021 Chiara Benzoni

ORCID

, Marco Moscatelli, Silvia Fenu, Anna Venerando, Ettore Salsano

ORCID

Correction to: Metachromatic leukodystrophy with late adult-onset: diagnostic clues and differences from other genetic leukoencephalopathies with dementia

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Valeria Bachiocco, Marco Cappa, Anna Petroni, Ettore Salsano

ORCID

, Carla Bizzarri, Ilaria Ceccarelli, Gabriele Cevenini, Viviana Pensato, Anna M. Aloisi

ORCID

Pain Study in X-Linked Adrenoleukodystrophy in Males and Females

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Chiara Benzoni

ORCID

, Marco Moscatelli, Silvia Fenu, Anna Venerando, Ettore Salsano

ORCID

Metachromatic leukodystrophy with late adult-onset: diagnostic clues and differences from other genetic leukoencephalopathies with dementia

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Davide Pareyson, Chiara Pantaleoni, Roberto Eleopra, Giuseppe De Filippis, Isabella Moroni, Elena Freri, Federica Zibordi, Sara Bulgheroni, Emanuela Pagliano, Daniela Sarti, Antonio Silvani, Licia Grazzi, Pietro Tiraboschi, C. Antozzi, A. Ardissone and 89 other authors

Neuro-telehealth for fragile patients in a tertiary referral neurological institute during the COVID-19 pandemic in Milan, Lombardy

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2020 Daniela Di Bella, Stefania Magri, Chiara Benzoni, Laura Farina, Carmelo Maccagnano, Elisa Sarto, Marco Moscatelli, Silvia Baratta, Claudia Ciano, Sylvie H. M. J. Piacentini, Lara Draghi, Elena Mauro, Davide Pareyson, Cinzia Gellera, Franco Taroni and 1 other authors

Hypomyelinating leukodystrophies in adults: clinical and genetic features

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

T. Bremova Ertl, L. Abel, M. Walterfang, E. Salsano

ORCID

, A. Ardissone, V. Malinová, M. Kolníková, Bayarri Jg, Tavasoli Ar, Ashrafi Mr, Y. Amraoui, E. Mengel, M. Strupp

Ocular motor biomarkers in Niemann-Pick disease type C: A prospective cross-sectional multicontinental study in 72 patients

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Stefania Bianchi-Marzoli, Silvia Fenu, Lisa Melzi, Chiara Benzoni, Filippo Antonazzo, Eugenia Tomas Roldan, Laura Farina, Gemma Tremolada, Elena Mauro, Viviana Pensato, Cinzia Gellera, Davide Pareyson, Ettore Salsano

ORCID

Optical coherence tomography in adult adrenoleukodystrophy: a cross-sectional and longitudinal study

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Letterio S. Politi, Ettore Salsano

ORCID

, Marco Grimaldi

Magnetic Resonance Imaging Alteration of the Brain in a Patient With Coronavirus Disease 2019 (COVID-19) and Anosmia

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Chiara Benzoni, Domenico Aquino, Daniela Di Bella, Elisa Sarto, Marco Moscatelli, Davide Pareyson, Franco Taroni, Ettore Salsano

ORCID

Severe worsening of adult-onset Alexander disease after minor head trauma: Report of two patients and review of the literature

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Chiara Benzoni, Silvia Fenu, Viviana Pensato, Elena Mauro, Cinzia Gellera, Davide Pareyson, Ettore Salsano

ORCID

Asymptomatic adrenoleukodystrophy in elderly males

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Viorica Chelban, Nicholas W. Wood

ORCID

, Miryam Carecchio

ORCID

, Gillian Rea, Abdalla Bowirrat, Salman Kirmani, Luca Magistrelli, Stephanie Efthymiou, Lucia Schottlaender, Luisa Chiapparini, Jana Vandrovcova, Farida Jan, Shahnaz Ibrahim, Vincenzo Salpietro, Fatima Khan and 11 other authors

MYORG-related disease is associated with central pontine calcifications and atypical parkinsonism

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

A. Potic, E. Salsano

ORCID

, C. Gellera, B. Castellotti, F. Taroni

Metabolic ataxia linked to new mutation in L2HGDH gene

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

C. Benzoni, S. Fenu, Pensato, D. Pareyson, E. Salsano

ORCID

Asymptomatic Adrenoleukodystrophy in Elderly Males

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2019 Ramona De Amicis

ORCID

, Alessandro Leone

ORCID

, Stefano Ravasenghi, Graziana Scigliuolo, Elena Mauro, Ettore Salsano

ORCID

, Alberto Battezzati

ORCID

, Simona Bertoli

ORCID

Triheptanoin Supplementation Does not Affect Nutritional Status: A Case Report of Two Siblings With Adult Polyglucosan Body Disease

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Lucia Corrado, Viviana Pensato, Roberta Croce, Alice Di Pierro, Simona Mellone, Eleonora Dalla Bella, Ettore Salsano

ORCID

, Elvezia Maria Paraboschi, Mara Giordano, Massimo Saraceno, Letizia Mazzini, Cinzia Gellera, Sandra D’Alfonso

The first case of the TARDBP p.G294V mutation in a homozygous state: is a single pathogenic allele sufficient to cause ALS?

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