Sara Satolli
Overview
Explore the profile of Sara Satolli including associated specialties, affiliations and a list of published articles.
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Articles
16
Citations
39
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Recent Articles
1.
Pagano S, Lopergolo D, De Falco A, Meossi C, Satolli S, Pasquariello R, et al.
Genes (Basel)
. 2025 Feb;
16(2).
PMID: 40004556
: Schuurs-Hoeijmakers syndrome (SHMS), also known as PACS1 neurodevelopmental disorder, is a rare condition characterized by intellectual disability, distinctive craniofacial abnormalities, and congenital malformations. SHMS has already been associated with...
2.
Satolli S, Rossi S, Boccuni L, Martinuzzi A, Musumeci O, Rizzo G, et al.
Neurol Sci
. 2025 Feb;
PMID: 39985651
No abstract available.
3.
Quazza F, Riant F, Patera M, Suppa A, Satolli S, Burglen L, et al.
Parkinsonism Relat Disord
. 2025 Feb;
132:107274.
PMID: 39908726
Background: ADCY5-related movement disorders are typically paroxysmal dyskinesia (PxDs) and/or static hyperkinetic movement disorders. Nocturnal paroxysmal dyskinesia (PxD), facial or perioral dyskinesia are suggestive of this genetic diagnosis. Next generation...
4.
Beichert L, Seemann J, Kessler C, Traschutz A, Muller D, Dillmann-Jehn K, et al.
Neurology
. 2024 Dec;
103(12):e209887.
PMID: 39621946
Background And Objectives: With targeted treatment trials on the horizon, identification of sensitive and valid outcome measures becomes a priority for >100 spastic ataxias. While digital-motor measures, assessed using wearable...
5.
Cappiello A, Cuoco S, De Micco R, Satolli S, Di Biasio F, Markushi T, et al.
Neurol Sci
. 2024 Nov;
46(3):1207-1215.
PMID: 39579261
Objectives: Neuropsychiatric symptoms, such as apathy, disinhibition and irritability, are common in Progressive Supranuclear Palsy (PSP). The Frontal Behaviour Inventory (FBI) is a useful instrument for the evaluation of behavioural...
6.
Satolli S, Rossi S, Vegezzi E, Pellerin D, Manca M, Barghigiani M, et al.
J Neurol
. 2024 Nov;
271(12):7650-7651.
PMID: 39499281
No abstract available.
7.
Papoff F, Astrea G, Mero S, Chicca L, Satolli S, Pasquariello R, et al.
Neuropediatrics
. 2024 Jul;
55(5):341-346.
PMID: 39059408
Hereditary spastic paraplegias (HSPs) are a genetically heterogeneous group of neurodegenerative disorders clinically characterized by progressive lower limb spasticity with pyramidal weakness. Around a dozen potential molecular mechanisms are recognized....
8.
Rigo M, Jin X, Godfrey L, Katz M, Sato H, Tomimatsu Y, et al.
Sci Rep
. 2024 Jul;
14(1):15574.
PMID: 38971867
The latest Triassic was characterised by protracted biotic extinctions concluding in the End-Triassic Extinction (~ 200 Ma) and a global carbon cycle perturbation. The onset of declining diversity is closely...
9.
Satolli S, Rossi S, Vegezzi E, Pellerin D, Manca M, Barghigiani M, et al.
J Neurol
. 2024 Jun;
271(8):5478-5488.
PMID: 38886208
Background: Autosomal-dominant spinocerebellar ataxia (ADCA) due to intronic GAA repeat expansion in FGF14 (SCA27B) is a recent, relatively common form of late-onset ataxia. Objective: Here, we aimed to: (1) investigate...
10.
Satolli S, De Micco R, Galatolo D, Tessa A, Cirillo M, Tessitore A, et al.
Mov Disord Clin Pract
. 2024 Jun;
11(9):1156-1159.
PMID: 38881152
No abstract available.