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Trovato, Rosanna
104  results:
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1

Hereditary spastic paraparesis type 18 (SPG18): new ERLIN2 ..:

Cioffi, Ettore ; Gioiosa, Valeria ; Tessa, Alessandra...
Neurological Sciences.  45 (2024)  8 - p. 3845-3852 , 2024
Link: https://doi.org/10.1007/..
 
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2

Power of NGS-based tests in HSP diagnosis: analysis of mass..:

Galatolo, Daniele ; Trovato, Rosanna ; Scarlatti, Arianna...
neurogenetics.  , 2023
Link: https://doi.org/10.1007/..
 
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3

A new genetic cause of spastic ataxia: the p.Glu415Lys vari..:

Torella, Annalaura ; Ricca, Ivana ; Piluso, Giulio...
Journal of Neurology.  270 (2023)  10 - p. 5057-5063 , 2023
Link: https://doi.org/10.1007/..
 
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4

CUL4B-associated epilepsy: Report of a novel truncating var..:

Della Vecchia, Stefania ; Lopergolo, Diego ; Trovato, Rosanna...
Seizure: European Journal of Epilepsy.  104 (2023)  - p. 32-37 , 2023
Link: https://doi.org/10.1016/..
 
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5

A Variant in TBCD Associated with Motoneuronopathy and Corp..:

Caputo, Maria ; Martinelli, Ilaria ; Fini, Nicola...
International Journal of Molecular Sciences.  24 (2023)  15 - p. 12386 , 2023
Link: https://doi.org/10.3390/..
 
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6

Neuroimaging patterns in paediatric onset hereditary spasti..:

Dosi, Claudia ; Pasquariello, Rosa ; Ticci, Chiara...
Journal of the Neurological Sciences.  425 (2021)  - p. 117441 , 2021
Link: https://doi.org/10.1016/..
 
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7

Spinocerebellar ataxia type 48: last but not least:

De Michele, Giovanna ; Galatolo, Daniele ; Barghigiani, Melissa...
Neurological Sciences.  41 (2020)  9 - p. 2423-2432 , 2020
Link: https://doi.org/10.1007/..
 
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8

Docosahexaenoic acid in ARSACS: observations in two patient:

Ricca, Ivana ; Tessa, Alessandra ; Trovato, Rosanna..
BMC Neurology.  20 (2020)  1 - p. , 2020
Link: https://doi.org/10.1186/..
 
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9

Multimodal evaluation of an Italian family with a hereditar..:

Ruggiero, Lucia ; Iovino, Aniello ; Dubbioso, Raffaele...
Annals of Clinical and Translational Neurology.  7 (2020)  11 - p. 2326-2331 , 2020
Link: https://doi.org/10.1002/..
 
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10

Congenital myopathies: clinical phenotypes and new diagnost..:

the Italian Network on Congenital Myopathies ; Cassandrini, Denise ; Trovato, Rosanna...
Italian Journal of Pediatrics.  43 (2017)  1 - p. , 2017
Link: https://doi.org/10.1186/..
 
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11

Myoimaging in the NGS era: the discovery of a novel mutatio..:

Astrea, Guja ; Petrucci, Antonio ; Cassandrini, Denise...
BMC Medical Genetics.  17 (2016)  1 - p. , 2016
Link: https://doi.org/10.1186/..
 
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12

A Diagnostic Dilemma in a Family With Cystinuria Type B Res..:

Astrea, Guja ; Munteanu, Iulia ; Cassandrini, Denise...
Pediatric Neurology.  52 (2015)  5 - p. 548-551 , 2015
Link: https://doi.org/10.1016/..
 
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13

Elevated Serum Creatine Kinase and Small Cerebellum Prompt ..:

Trovato, Rosanna ; Astrea, Guja ; Bartalena, Laura...
Journal of Child Neurology.  29 (2013)  3 - p. 394-398 , 2013
Link: https://doi.org/10.1177/..
 
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14

EXOSC3 mutations in isolated cerebellar hypoplasia and spin..:

Biancheri, Roberta ; Cassandrini, Denise ; Pinto, Francesca...
Journal of Neurology.  260 (2013)  7 - p. 1866-1870 , 2013
Link: https://doi.org/10.1007/..
 
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15

A new genetic cause of spastic ataxia: the p.Glu415Lys vari..:

Torella, Annalaura ; Ricca, Ivana ; Piluso, Giulio...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10511369/.  , 2023
Link: http://www.ncbi.nlm.nih...
 
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