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Garone, Giacomo
65
results:
Search for persons
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Format
Online (65)
Mediatypes
Articles (Online) (33)
OpenAccess-fulltext (32)
Languages
english (55)
french (1)
Sorted by: Relevance
Sorted by: Year
?
1
Pediatric torticollis: clinical report and predictors of ur..:
Raucci, Umberto
;
Roversi, Marco
;
Ferretti, Alessandro
...
Italian Journal of Pediatrics. 50 (2024) 1 - p. , 2024
Link:
https://doi.org/10.1186/..
?
2
Spectrum of ERCC6-Related Cockayne Syndrome (Type B): From ..:
Sartorelli, Jacopo
;
Travaglini, Lorena
;
Macchiaiolo, Marina
...
Genes. 15 (2024) 4 - p. 508 , 2024
Link:
https://doi.org/10.3390/..
?
3
Movement disorder phenotype in CTNNB1-syndrome: a complex b..:
Garone, Giacomo
;
Innocenti, Alice
;
Grasso, Melissa
...
Parkinsonism & Related Disorders. , 2024
Link:
https://doi.org/10.1016/..
?
4
BCL11B‐Related Dystonia: Further Evidence of an Emerging Ca..:
Garone, Giacomo
;
Capuano, Alessandro
;
Amodio, Donato
...
Movement Disorders Clinical Practice. 11 (2024) 7 - p. 897-901 , 2024
Link:
https://doi.org/10.1002/..
?
5
Case Report: A rare form of congenital erythrocytosis due t..:
Giannini, Rosalinda
;
Agolini, Emanuele
;
Palumbo, Giuseppe
...
Frontiers in Pediatrics. 12 (2024) - p. , 2024
Link:
https://doi.org/10.3389/..
?
6
Dyskinetic crisis in GNAO1-related disorders: clinical pers..:
Domínguez Carral, Jana
;
Reinhard, Carola
;
Ebrahimi-Fakhari, Darius
...
Frontiers in Neurology. 15 (2024) - p. , 2024
Link:
https://doi.org/10.3389/..
?
7
Movement Disorders in Patients With Genetic Developmental a..:
van der Veen, Sterre
;
Tse, Gabrielle T.W.
;
Ferretti, Alessandro
...
Neurology. 101 (2023) 19 - p. , 2023
Link:
https://doi.org/10.1212/..
?
8
Congenital heart defects in CTNNB1 syndrome: Raising clinic..:
Sinibaldi, Lorenzo
;
Garone, Giacomo
;
Mandarino, Alessandra
...
Clinical Genetics. 104 (2023) 5 - p. 528-541 , 2023
Link:
https://doi.org/10.1111/..
?
9
Acute Pupillary Disorders in Children: A 10-Year Retrospect..:
Garone, Giacomo
;
Roversi, Marco
;
Pisani, Mara
...
Children. 10 (2023) 11 - p. 1739 , 2023
Link:
https://doi.org/10.3390/..
?
10
Expansion du phénotype dystonique associé aux mutations dan..:
Wirth, Thomas
;
Garone, Giacomo
;
Amélie, Piton
...
Revue Neurologique. 178 (2022) - p. S44 , 2022
Link:
https://doi.org/10.1016/..
?
11
Reply to: "GNAO1 Haploinsufficiency Associated with a Mild ..:
Wirth, Thomas
;
Garone, Giacomo
;
Kurian, Manju A.
...
Movement Disorders. 37 (2022) 12 - p. 2466-2467 , 2022
Link:
https://doi.org/10.1002/..
?
12
"Spazio Huntington": Tracing the Early Motor, Cognitive and..:
Graziola, Federica
;
Maffi, Sabrina
;
Grasso, Melissa
...
Journal of Personalized Medicine. 12 (2022) 1 - p. 120 , 2022
Link:
https://doi.org/10.3390/..
?
13
Highlighting the Dystonic Phenotype Related to GNAO1:
Wirth, Thomas
;
Garone, Giacomo
;
Kurian, Manju A.
...
Movement Disorders. 37 (2022) 7 - p. 1547-1554 , 2022
Link:
https://doi.org/10.1002/..
?
14
Cognitive deficits in childrens with brain tumours: A proje..:
Mastronuzzi, Angela
;
Secco, Domitilla Elena
;
Laus, Beatrice
...
Journal of the Neurological Sciences. 429 (2021) - p. 118451 , 2021
Link:
https://doi.org/10.1016/..
?
15
Cognitive Assessment in GNAO1 Neurodevelopmental Disorder U..:
Graziola, Federica
;
Garone, Giacomo
;
Grasso, Melissa
.
Journal of Clinical Medicine. 10 (2021) 16 - p. 3541 , 2021
Link:
https://doi.org/10.3390/..
1-15