Giuseppe Novelli
Overview
Explore the profile of Giuseppe Novelli including associated specialties, affiliations and a list of published articles.
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Articles
415
Citations
8907
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Recent Articles
21.
Vancheri C, Quatrana A, Morini E, Mariotti C, Mongelli A, Fichera M, et al.
Hum Genomics
. 2024 May;
18(1):50.
PMID: 38778374
Friedreich ataxia (FRDA) is a life-threatening hereditary ataxia; its incidence is 1:50,000 individuals in the Caucasian population. A unique therapeutic drug for FRDA, the antioxidant Omaveloxolone, has been recently approved...
22.
De Benedittis G, DAntonio A, Latini A, Morgante C, Conigliaro P, Triggianese P, et al.
Int Immunopharmacol
. 2024 May;
134:112239.
PMID: 38761785
We aimed to identify an expression profile of lncRNAs potentially related to treatment response in Psoriatic arthritis (PsA) patients, to be used as potential genomic biomarkers predictors of drug treatment...
23.
Graziani L, Nuovo S, Pisaneschi E, Carriero M, Baghernajad Salehi L, Nardone A, et al.
J Matern Fetal Neonatal Med
. 2024 Apr;
37(1):2344718.
PMID: 38679587
Objective: Holoprosencephaly (HPE) is the most common aberration of forebrain development, and it leads to a wide spectrum of developmental and craniofacial anomalies. HPE etiology is highly heterogeneous and includes...
24.
Kirkpatrick A, Coccolini F, Tolonen M, Minor S, Catena F, Celotti A, et al.
J Clin Med
. 2024 Feb;
13(4).
PMID: 38398318
Ventral incisional hernias are common indications for elective repair and frequently complicated by recurrence. Surgical meshes, which may be synthetic, bio-synthetic, or biological, decrease recurrence and, resultingly, their use has...
25.
Latini A, De Benedittis G, Conigliaro P, Bonini C, Morgante C, Iacovantuono M, et al.
Genes (Basel)
. 2024 Feb;
15(2).
PMID: 38397223
The vitamin D receptor (VDR), binding to the active form of the vitamin, promotes the transcription of numerous genes involved in the proliferation of immune cells, cytokine production and lymphocyte...
26.
Minotti C, Graziani L, Sallicandro E, Digilio M, Falasca R, Alesi V, et al.
Front Genet
. 2024 Feb;
14:1315291.
PMID: 38380230
Interstitial deletions involving 6q chromosomal region are rare. Less than 30 patients have been described to date, and fewer have been characterized by high-resolution techniques, such as chromosomal microarray. Deletions...
27.
Latini A, Borgiani P, De Benedittis G, Ciccacci C, Novelli L, Pepe G, et al.
Gene
. 2024 Feb;
907:148279.
PMID: 38360126
The identification of rare genetic variants associated to Systemic Lupus Erythematosus (SLE) could also help to understand the pathogenic mechanisms at the basis of the disease. In this study we...
28.
Latini A, De Benedittis G, Ciccacci C, Novelli G, Spallone V, Borgiani P
Epigenomics
. 2024 Jan;
16(2):85-91.
PMID: 38221897
This study investigated a possible correlation between three circulating miRNAs, previously observed to be associated to diabetic polyneuropathy, and the obesity condition. The expression levels of miR-128a, miR-155 and miR499a...
29.
Matuozzo D, Talouarn E, Marchal A, Zhang P, Manry J, Seeleuthner Y, et al.
Genome Med
. 2024 Jan;
16(1):6.
PMID: 38184654
No abstract available.
30.
Ferese R, Scala S, Suppa A, Campopiano R, Asci F, Zampogna A, et al.
Front Neurol
. 2023 Dec;
14:1296924.
PMID: 38145127
Introduction: Pure hereditary spastic paraplegia (SPG) type 4 (SPG4) is caused by mutations of gene. This study aimed to analyze variants in SPG4 patients to highlight the occurrence of splicing...