Zobrazeno 1 - 10
of 55
pro vyhledávání: '"Vincenzo Montano"'
Autor:
Piervito Lopriore, Valentina Ricciarini, Gabriele Siciliano, Michelangelo Mancuso, Vincenzo Montano
Publikováno v:
Neurology International, Vol 14, Iss 2, Pp 337-356 (2022)
Ataxia is increasingly being recognized as a cardinal manifestation in primary mitochondrial diseases (PMDs) in both paediatric and adult patients. It can be caused by disruption of cerebellar nuclei or fibres, its connection with the brainstem, or s
Externí odkaz:
https://doaj.org/article/e7fa3f7d3a72483690177dc19a93bbe4
Autor:
Daniele Orsucci, Elena Caldarazzo Ienco, Vincenzo Montano, Gabriele Siciliano, Michelangelo Mancuso
Publikováno v:
Pharmacological Research, Vol 180, Iss , Pp 106228- (2022)
A mitochondrial stroke-like event is an evolving subacute neurological syndrome linked to seizure activity and focal metabolic brain derangement in a genetically determined mitochondrial disorder. The acronym “MELAS” (mitochondrial encephalopathy
Externí odkaz:
https://doaj.org/article/c4f05499d74a4474ab21b35ec659b677
Autor:
Vincenzo, Montano, Michelangelo, Mancuso, Costanza, Simoncini, Francesca, Torri, Lucia, Chico, Greta, Ali, Anna, Rocchi, Fulvia, Baldinotti, Maria Adelaide, Caligo, Giovanna, Lattanzi, Elisabetta, Mattioli, Giovanna, Cenacchi, Andrea, Barison, Gabriele, Siciliano, Giulia, Ricci
Publikováno v:
Journal of Neuromuscular Diseases. 9:457-462
Background: Proximal muscle weakness may be the presenting clinical feature of different types of myopathies, including limb girdle muscular dystrophy and primary mitochondrial myopathy. LGMD1B is caused by LMNA mutation. It is characterized by progr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8088f253ee11280a5c1c981ab6e27b10
https://doi.org/10.3233/jnd-220802
https://doi.org/10.3233/jnd-220802
Autor:
Domenico Giannese, Vincenzo Montano, Piervito Lopriore, Claudia Nesti, Annalisa LoGerfo, Maria Adelaide Caligo, Flavio Dal Canto, Gianandrea Pasquinelli, Angelo Giovanni Bonadio, Diego Moriconi, Gabriele Siciliano, Michelangelo Mancuso
Publikováno v:
Journal of neuromuscular diseases. 10(1)
Background: Mitochondrial tRNA (MTT) genes are hotspot for mitochondrial DNA mutation and are responsible of half mitochondrial disease. MTT mutations are associated with a broad spectrum of phenotype often with complex multisystem involvement and co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::678dcc16818ec54383bc2c1de6de834b
https://pubmed.ncbi.nlm.nih.gov/36404555
https://pubmed.ncbi.nlm.nih.gov/36404555
Autor:
Mirco Cosottini, Graziella Donatelli, Ivana Ricca, Francesca Bianchi, Daniela Frosini, Vincenzo Montano, Gianmichele Migaleddu, Eleonora Del Prete, Alessandra Tessa, Paolo Cecchi, Claudio D’Amelio, Gabriele Siciliano, Michelangelo Mancuso, Filippo Maria Santorelli
Publikováno v:
European radiology. 32(12)
Hereditary spastic paraplegia (HSP) is a group of genetic neurodegenerative diseases characterised by upper motor neuron (UMN) impairment of the lower limbs. The differential diagnosis with primary lateral sclerosis (PLS) and amyotrophic lateral scle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af0169497de26db1b87f085506d61eac
https://pubmed.ncbi.nlm.nih.gov/36074266
https://pubmed.ncbi.nlm.nih.gov/36074266
Primary mitochondrial diseases are relatively common inborn errors of energy metabolism, with a combined prevalence of 1 in 4300. These disorders typically affect tissues with high energy requirements, including the brain. Epilepsy affects >1% of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6cf8e761dd43284fd3680171acbdaaba
https://hdl.handle.net/11568/1156510
https://hdl.handle.net/11568/1156510
Autor:
Daniele, Orsucci, Elena, Caldarazzo Ienco, Vincenzo, Montano, Gabriele, Siciliano, Michelangelo, Mancuso
A mitochondrial stroke-like event is an evolving subacute neurological syndrome linked to seizure activity and focal metabolic brain derangement in a genetically determined mitochondrial disorder. The acronym "MELAS" (mitochondrial encephalopathy ass
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ac4870ac260418c9a1babde28d61c4d
http://hdl.handle.net/11568/1139014
http://hdl.handle.net/11568/1139014
Autor:
Francesca Torri, Piervito Lopriore, Vincenzo Montano, Gabriele Siciliano, Michelangelo Mancuso, Giulia Ricci
Publikováno v:
International Journal of Molecular Sciences. 24:5005
Fatigue is a major determinant of quality of life and motor function in patients affected by several neuromuscular diseases, each of them characterized by a peculiar physiopathology and the involvement of numerous interplaying factors. This narrative
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa2992c0ece6ff3d08db171bb0521ace
https://doi.org/10.3390/ijms24055005
https://doi.org/10.3390/ijms24055005
Autor:
Sam M. H. Does, Max M. B. Wempe, Santiago J. Garcia, Sybrand van der Zwaag, Johan Bijleveld, Vincenzo Montano
Publikováno v:
Macromolecules, 52(21)
Macromolecules
Macromolecules
In this work, we propose the use of regular branching of polyurethanes as a way to regulate chain dynamics and govern crystallization in highly dense hydrogen-bonded systems. As a result, robust and healable polyurethanes can be obtained. To this end
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46f560e6c9064bb9bc57c40e5e249e60
https://doi.org/10.1021/acs.macromol.9b01554
https://doi.org/10.1021/acs.macromol.9b01554
Publikováno v:
Physical chemistry chemical physics (PCCP), 21(19)
Starting from experimental macro-rheological data, we develop a fitting protocol that succeeded in the separation of the overlapping relaxation phenomena in the dissipative regime for a set of intrinsic healing polymers healing most effectively near
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::beee278f73d21ec0d37fe19ef7df4e34
https://doi.org/10.1039/c9cp00417c
https://doi.org/10.1039/c9cp00417c