Giuseppe De Michele
Overview
Explore the profile of Giuseppe De Michele including associated specialties, affiliations and a list of published articles.
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Articles
174
Citations
2604
Followers
0
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Recent Articles
1.
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.
2.
Giglio A, Russo C, Riccio G, Braca S, Cretella G, Stornaiuolo A, et al.
Neurol Sci
. 2024 Oct;
45(12):5749-5756.
PMID: 39432180
Introduction: Parkinson's disease (PD) is characterized by the progressive loss of dopaminergic neurons in the substantia nigra, but dopamine also plays a role in the pathophysiology of migraine. Objective: The...
3.
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...
4.
Horta-Barba A, Martinez-Horta S, Perez-Perez J, Puig-Davi A, De Lucia N, De Michele G, et al.
J Neurol
. 2023 Jul;
270(11):5408-5417.
PMID: 37462754
Background: Progressive cognitive decline is an inevitable feature of Huntington's disease (HD) but specific criteria and instruments are still insufficiently developed to reliably classify patients into categories of cognitive severity...
5.
Torella A, Ricca I, Piluso G, Galatolo D, De Michele G, Zanobio M, et al.
J Neurol
. 2023 Jul;
270(10):5057-5063.
PMID: 37418012
Tubulinopathies encompass neurodevelopmental disorders caused by mutations in genes encoding for different isotypes of α- and β-tubulins, the structural components of microtubules. Less frequently, mutations in tubulins may underlie neurodegenerative...
6.
De Lucia N, De Rosa A, Perillo S, Sperandeo R, De Michele G, Maldonato N
J Neuropsychiatry Clin Neurosci
. 2023 Mar;
35(3):228-235.
PMID: 36999250
Objective: Personality changes have often been reported among people with Parkinson's disease (PD); however, no studies have investigated the associations between personality traits, cognitive function, and specific motor symptoms. In...
7.
De Michele G, Maione L, Cocozza S, Tranfa M, Pane C, Galatolo D, et al.
Cerebellum
. 2023 Mar;
23(2):688-701.
PMID: 36997834
The association of hypogonadism and cerebellar ataxia was first recognized in 1908 by Gordon Holmes. Since the seminal description, several heterogeneous phenotypes have been reported, differing for age at onset,...
8.
Vollstedt E, Schaake S, Lohmann K, Padmanabhan S, Brice A, Lesage S, et al.
Mov Disord
. 2023 Jan;
38(2):286-303.
PMID: 36692014
Background: As gene-targeted therapies are increasingly being developed for Parkinson's disease (PD), identifying and characterizing carriers of specific genetic pathogenic variants is imperative. Only a small fraction of the estimated...
9.
De Michele G, Palmieri G, Pane C, Valente E, Palmieri I, Dello Iacovo C, et al.
Acta Neurol Belg
. 2023 Jan;
123(1):221-226.
PMID: 36609835
Background: Mutations of the Glucocerebrosidase (GBA) gene are the most common genetic risk factor yet discovered for Parkinson's Disease (PD), being found in about 5-14% of Caucasian patients. Objective: We...
10.
Perillo S, Palmieri G, Del Moral M, De Michele G, Giglio A, Cuomo N, et al.
Neurol Sci
. 2022 Dec;
44(4):1235-1241.
PMID: 36547780
Background: So far, mutations in genes encoding lysosomal enzymes have been associated with Parkinson's disease (PD). Fabry disease (FD) is an X-linked lysosomal storage disease caused by alpha-galactosidase A (α-GAL)...