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Jacopo Baldacci
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1

Correction to: Monoallelic KIF1A-related disorders: a multi..:

Della Vecchia, Stefania ; Tessa, Alessandra ; Dosi, Claudia...
Journal of Neurology.  270 (2023)  4 - p. 2345-2346 , 2023
Link: https://doi.org/10.1007/..
 
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2

Using Cluster Analysis to Overcome the Limits of Traditiona..:

Dosi, Claudia ; Rubegni, Anna ; Baldacci, Jacopo...
Genes.  14 (2023)  2 - p. 298 , 2023
Link: https://doi.org/10.3390/..
 
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3

Automatic Recognition of Ragged Red Fibers in Muscle Biopsy..:

Baldacci, Jacopo ; Calderisi, Marco ; Fiorillo, Chiara..
Healthcare.  10 (2022)  3 - p. 574 , 2022
Link: https://doi.org/10.3390/..
 
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4

The Diagnostic Approach to Mitochondrial Disorders in Child..:

Tolomeo, Deborah ; Orsucci, Daniele ; Nesti, Claudia...
Journal of Clinical Medicine.  10 (2021)  15 - p. 3222 , 2021
Link: https://doi.org/10.3390/..
 
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5

Bi‐allelic variants in MDH2: Expanding the clinical phenoty..:

Ticci, Chiara ; Nesti, Claudia ; Rubegni, Anna...
Clinical Genetics.  101 (2021)  2 - p. 260-264 , 2021
Link: https://doi.org/10.1111/..
 
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6

Correction to: Monoallelic KIF1A-related disorders: a multi..:

Della Vecchia, Stefania ; Tessa, Alessandra ; Dosi, Claudia...
Journal of Neurology.  269 (2021)  1 - p. 451-451 , 2021
Link: https://doi.org/10.1007/..
 
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7

Expanding the clinical and genetic spectrum of pathogenic v..:

Ticci, Chiara ; Cassandrini, Denise ; Rubegni, Anna...
Muscle & Nerve.  64 (2021)  5 - p. 567-575 , 2021
Link: https://doi.org/10.1002/..
 
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8

Monoallelic KIF1A-related disorders: a multicenter cross se..:

Vecchia, Stefania Della ; Tessa, Alessandra ; Dosi, Claudia...
Journal of Neurology.  269 (2021)  1 - p. 437-450 , 2021
Link: https://doi.org/10.1007/..
 
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9

Loss of ap4s1 in zebrafish leads to neurodevelopmental defe..:

D'Amore, Angelica ; Tessa, Alessandra ; Naef, Valentina...
Annals of Clinical and Translational Neurology.  7 (2020)  4 - p. 584-589 , 2020
Link: https://doi.org/10.1002/..
 
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10

Complex multisystem phenotype associated with the mitochond..:

Nesti, Claudia ; Rubegni, Anna ; Tolomeo, Deborah...
Neurological Sciences.  40 (2019)  8 - p. 1705-1708 , 2019
Link: https://doi.org/10.1007/..
 
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11

Autophagic vacuolar myopathy caused by a CLN3 mutation. A c..:

Moro, Francesca ; Rubegni, Anna ; Pochiero, Francesca...
Neuromuscular Disorders.  29 (2019)  1 - p. 67-69 , 2019
Link: https://doi.org/10.1016/..
 
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12

Spinocerebellar ataxia 48 presenting with ataxia associated..:

De Michele, Giovanna ; Lieto, Maria ; Galatolo, Daniele...
Parkinsonism & Related Disorders.  65 (2019)  - p. 91-96 , 2019
Link: https://doi.org/10.1016/..
 
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13

Clinical and neuroimaging features of autosomal recessive s..:

Mari, Francesco ; Berti, Beatrice ; Romano, Alessandro...
neurogenetics.  19 (2018)  2 - p. 123-130 , 2018
Link: https://doi.org/10.1007/..
 
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14

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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15

Dolichol-phosphate mannose synthase depletion in zebrafish ..:

Marchese, Maria ; Pappalardo, Andrea ; Baldacci, Jacopo...
Biochemical and Biophysical Research Communications.  477 (2016)  1 - p. 137-143 , 2016
Link: https://doi.org/10.1016/..
 
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