Carolina Frassoni
Overview
Explore the profile of Carolina Frassoni including associated specialties, affiliations and a list of published articles.
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40
Citations
732
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Recent Articles
1.
Foglio B, Rossini L, Garbelli R, Regondi M, Mercurio S, Bertacchi M, et al.
Brain Struct Funct
. 2021 Mar;
226(4):1303-1322.
PMID: 33661352
The neocortex, the most recently evolved brain region in mammals, is characterized by its unique areal and laminar organization. Distinct cortical layers and areas can be identified by the presence...
2.
Moroni R, Regondi M, de Curtis M, Frassoni C, Librizzi L
Neuroscience
. 2020 Jun;
441:65-76.
PMID: 32590038
Astrocyte dysfunction, and in particular impaired extracellular potassium spatial buffering, has been postulated to have a potential role in seizure susceptibility and ictogenesis. Inwardly rectifying potassium (Kir) channels, and specifically...
3.
Bertacchi M, Romano A, Loubat A, Mau-Them F, Willems M, Faivre L, et al.
EMBO J
. 2020 Jun;
39(13):e104163.
PMID: 32484994
The relationships between impaired cortical development and consequent malformations in neurodevelopmental disorders, as well as the genes implicated in these processes, are not fully elucidated to date. In this study,...
4.
Mercurio S, Serra L, Motta A, Gesuita L, Sanchez-Arrones L, Inverardi F, et al.
iScience
. 2019 May;
15:257-273.
PMID: 31082736
Visual system development involves the formation of neuronal projections connecting the retina to the thalamic dorso-lateral geniculate nucleus (dLGN) and the thalamus to the visual cerebral cortex. Patients carrying mutations...
5.
Salgueiro-Pereira A, Duprat F, Pousinha P, Loucif A, Douchamps V, Regondi C, et al.
Neurobiol Dis
. 2019 Jan;
125:31-44.
PMID: 30659983
SCN1A (Na1.1 sodium channel) mutations cause Dravet syndrome (DS) and GEFS+ (which is in general milder), and are risk factors in other epilepsies. Phenotypic variability limits precision medicine in epilepsy,...
6.
Sanavio B, Librizzi L, Pennacchio P, Beznoussenko G, Sousa F, Silva P, et al.
Nanoscale
. 2018 Nov;
10(47):22420-22428.
PMID: 30475372
Diagnosis and treatment of brain disorders, such as epilepsy, neurodegenerative diseases and tumors, would benefit from innovative approaches to deliver therapeutic or diagnostic compounds into the brain parenchyma, with either...
7.
Moroni R, Deleo F, Regondi M, Madaschi L, Amadeo A, Frassoni C
Brain Struct Funct
. 2018 Aug;
223(9):4053-4066.
PMID: 30132245
The postnatal brain development is characterized by a substantial gain in weight and size, ascribed to increasing neuronal size and branching, and to massive addition of glial cells. This occurs...
8.
Frassoni C, Avagliano L, Inverardi F, Spaccini L, Parazzini C, Rustico M, et al.
Neuropediatrics
. 2016 May;
47(4):253-8.
PMID: 27177044
The development of the human cerebral cortex is a complex and precisely programmed process by which alterations may lead to morphological and functional neurological abnormalities. We report familial cases of...
9.
Righini A, Cesaretti C, Conte G, Parazzini C, Frassoni C, Bulfamante G, et al.
Neuroradiology
. 2015 Nov;
58(3):293-300.
PMID: 26608601
Introduction: Ganglionic eminence (GE) is a transient fetal brain structure that harvests a significant amount of precursors of cortical GABA-ergic interneurons. Prenatal magnetic resonance (MR) imaging features of GE anomalies...
10.
Moroni R, Inverardi F, Regondi M, Pennacchio P, Frassoni C
Int J Dev Neurosci
. 2015 Oct;
47(Pt B):198-205.
PMID: 26427731
Kir4.1 is the principal K(+) channel expressed in glial cells. It has been shown that it plays a fundamental role in K(+)-spatial buffering, an astrocyte-specific process where excess extracellular concentration...