Elisabetta Morini
Overview
Explore the profile of Elisabetta Morini including associated specialties, affiliations and a list of published articles.
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Articles
36
Citations
263
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Recent Articles
1.
Yun S, Chekuri A, Art J, Kondabolu K, Slaugenhaupt S, Zeltner N, et al.
bioRxiv
. 2024 Dec;
PMID: 39651221
Familial dysautonomia (FD) is a fatal autosomal recessive congenital neuropathy caused by a T-to-C mutation in intron 20 of the () gene, which causes tissue-specific skipping of exon 20 and...
2.
Harripaul R, Morini E, Salani M, Logan E, Kirchner E, Bolduc J, et al.
Sci Rep
. 2024 May;
14(1):10103.
PMID: 38698036
No abstract available.
3.
Veneziani I, Grimaldi A, Marra A, Morini E, Culicetto L, Marino S, et al.
J Clin Med
. 2024 Apr;
13(8).
PMID: 38673581
: Several studies have shown a relation between obesity and cognitive decline, highlighting a significant global health challenge. In recent years, artificial intelligence (AI) and machine learning (ML) have been...
4.
McLean Z, Gao D, Correia K, Roy J, Shibata S, Farnum I, et al.
Nat Commun
. 2024 Apr;
15(1):3182.
PMID: 38609352
Huntington's disease (HD) is a dominant neurological disorder caused by an expanded HTT exon 1 CAG repeat that lengthens huntingtin's polyglutamine tract. Lowering mutant huntingtin has been proposed for treating...
5.
Tai D, Razaz P, Erdin S, Gao D, Wang J, Nuttle X, et al.
Am J Hum Genet
. 2024 Mar;
111(3):619.
PMID: 38458168
No abstract available.
6.
Rondanelli M, Minisola S, Barale M, Barbaro D, Mansueto F, Battaglia S, et al.
Aging Clin Exp Res
. 2024 Feb;
36(1):38.
PMID: 38345765
Background: Osteoporosis is a common concern in the elderly that leads to fragile bones. Calcium supplementation plays a crucial role in improving bone health, reducing fracture risk, and supporting overall...
7.
Harripaul R, Morini E, Salani M, Logan E, Kirchner E, Bolduc J, et al.
Sci Rep
. 2024 Jan;
14(1):570.
PMID: 38177237
Familial dysautonomia (FD) is a rare recessive neurodevelopmental disease caused by a splice mutation in the Elongator acetyltransferase complex subunit 1 (ELP1) gene. This mutation results in a tissue-specific reduction...
8.
Schultz A, Cheng S, Kirchner E, Costello S, Miettinen H, Chaverra M, et al.
Sci Rep
. 2023 Oct;
13(1):18600.
PMID: 37903840
Familial dysautonomia (FD) is a rare neurodevelopmental and neurodegenerative disease caused by a splicing mutation in the Elongator Acetyltransferase Complex Subunit 1 (ELP1) gene. The reduction in ELP1 mRNA and...
9.
Harripaul R, Morini E, Salani M, Logan E, Kirchner E, Bolduc J, et al.
bioRxiv
. 2023 Oct;
PMID: 37808686
Familial dysautonomia (FD) is a rare recessive neurodevelopmental disease caused by a splice mutation in the Elongator acetyltransferase complex subunit 1 ( ) gene. This mutation results in a tissue-specific...
10.
McLean Z, Gao D, Correia K, Roy J, Shibata S, Farnum I, et al.
bioRxiv
. 2023 Aug;
PMID: 37547003
Huntington's disease (HD) is a dominantly inherited neurodegenerative disorder whose motor, cognitive, and behavioral manifestations are caused by an expanded, somatically unstable CAG repeat in the first exon of that...