Ettore Salsano - Dissemin

Papers authored by Ettore Salsano

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2019 Marisa I. Mendes, Lydia M. C. Green, Enrico Bertini, Davide Tonduti, Chiara Aiello, Sarah von Spiczak, Desiree Smith, Ettore Salsano

, Shanice Beerepoot

, Jozef Hertecant, Sarah Spiczak, John H. Livingston, Lisa Emrick, Jamie Fraser, Laura Russell and 19 other authors

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João Durães

, Ettore Salsano

, Maria do Carmo Macário

Adult-onset Krabbe disease

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Chiara Benzoni, Laura Farina, Viviana Pensato, Giorgio Marotta, Altin Kuqo, Elena Mauro, Davide Pareyson, Ettore Salsano

Leukoencephalopathy With Predominant Infratentorial Involvement Caused by a Novel ABCD1 Mutation

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Marta Gatti, Stefania Magri, Lorenzo Nanetti, Elisa Sarto, Daniela Di Bella, Ettore Salsano

, Chiara Pantaleoni, Caterina Mariotti

, Franco Taroni

From congenital microcephaly to adult onset cerebellar ataxia: Distinct and overlapping phenotypes in patients with PNKP gene mutations

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Silvia Masnada, Stefan Groenweg, Veronica Saletti, Luisa Chiapparini, Barbara Castellotti, Ettore Salsano

, W. Edward Visser, Davide Tonduti

Novel mutations in SLC16A2 associated with a less severe phenotype of MCT8 deficiency

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Silvia Fenu, Barbara Castellotti, Laura Farina, Tiziana Cavallaro, Daniela Di Bella, Chiara Benzoni, Cinzia Gellera, Davide Pareyson, Franco Taroni, Ettore Salsano

Saposin B deficiency as a cause of adult-onset metachromatic leukodystrophy

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Luigi Caputi, Alessandra Erbetta, Gianluca Marucci, Davide Pareyson, Marica Eoli, Maura Servida, Eugenio Parati, Ettore Salsano

Biopsy-proven primary angiitis of the central nervous system mimicking leukodystrophy: A case report and review of the literature

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Lara Draghi

, Ettore Salsano

, Laura Farina, Daniela Di Bella, Silvia Fenu, Davide Pareyson, Franco Taroni, Sylvie H. M. J. Piacentini

Neuropsychological features of adult form of Alexander disease

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L. S. Politi

, A. Castellano, N. Papinutto, E. Mauro, D. Pareyson, R. G. Henry, A. Falini, E. Salsano

Longitudinal quantitative magnetic resonance imaging in adrenomyeloneuropathy

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S. Magri, D. Di Bella, E. Sarto, F. Balistreri, S. Baratta, D. Tonduti, L. Nanetti, E. Salsano

, I. Moroni, C. Pisciotta, D. Pareyson, C. Mariotti, C. Gellera, F. Taroni

NGS gene panels for the challenging diagnosis of neurodegenerative disorders with high genetic heterogeneity

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E. Salsano

, D. Di Bella, S. Magri, L. Farina, C. Benzoni, S. Fenu, E. Mauro, C. Gellera, D. Pareyson, F. Taroni

Subclinical diffuse leukoencephalopathy: proposal for a new entity

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D. Di Bella, S. Magri, E. Sarto, D. Tonduti, A. Simonati, I. Moroni, C. Gellera, E. Salsano

, F. Taroni

An NGS approach to the genetic diagnosis of hereditary leukodystrophies

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2018 Cecilia Marelli, Ettore Salsano

, Letterio S. Politi, Pierre Labauge

Spinal cord involvement in adult-onset metabolic and genetic diseases

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Distributing this paper is prohibited by the publisher

Letterio S. Politi, Ettore Salsano

, Alessandra Biffi

Metachromatic Leukodystrophy

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Eliana Marisa Ramos, Miryam Carecchio, Roberta Lemos, Ramos Em, Joana Ferreira, Renee Louise Sears, Andrea Legati, Christine Tranchant, Sandy Chan Hsu, Celeste Panteghini, Marie Vidailhet, David Wallon, Anne-Claire Richard, Luca Magistrelli, Ettore Salsano

and 27 other authors

Primary brain calcification: an international study reporting novel variants and associated phenotypes

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Veronica Redaelli, Ettore Salsano

, Lara Colleoni, Paola Corbetta, Giovanni Tringali, Angelo Del Sole, Giorgio Giaccone, Giacomina Rossi

Frontotemporal Dementia and Chorea Associated with a Compound Heterozygous TREM2 Mutation

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A. Potic, Pensato, A. Rovelli, E. Salsano

X-linked Adrenoleukodystrophy: a metabolic disorder in young male psychiatric patients

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2017 Luisa Chiapparini

, G. de Luca

, Giulio Cavalli

, Tiziana Langella, Anna Venerando, Giacomo De Luca, Sergio Raspante, Giorgio Marotta, Bianca Pollo, Giuseppe Lauria, Maria Giulia Cangi, Simonetta Gerevini

, Andrea Botturi, Davide Pareyson, Lorenzo Dagna and 1 other authors

Adult leukoencephalopathies with prominent infratentorial involvement can be caused by Erdheim–Chester disease

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Marco Castori, Silvia Morlino, Martin Ungelenk, Davide Pareyson, Ettore Salsano

, Paola Grammatico, Emanuela Tolosano, Ingo Kurth, Deborah Chiabrando

Posterior column ataxia with retinitis pigmentosa coexisting with sensory-autonomic neuropathy and leukemia due to the homozygous p.Pro221Ser FLVCR1 mutation

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G. M. Scigliuolo, A. Sagnelli, G. Brenna, D. Pareyson, E. Salsano

Lack of benefit of acetyl- dl -leucine in patients with multiple system atrophy of the cerebellar type

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Papers authored by Ettore Salsano