Laura Bernardini
Overview
Explore the profile of Laura Bernardini including associated specialties, affiliations and a list of published articles.
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Articles
148
Citations
1584
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Recent Articles
11.
Rallis D, Ben-David D, Woo K, Robinson J, Beadles D, Bernardini L, et al.
Front Pediatr
. 2024 Jan;
11:1326668.
PMID: 38239592
Objectives: To examine whether first-intention high-frequency jet ventilation (HFVJ), compared to volume-targeted ventilation (VTV), in extremely preterm infants is associated with lower incidence of bronchopulmonary dysplasia (BPD) and other adverse...
12.
Guadagnolo D, Mastromoro G, Torres B, Marchionni E, di Palma F, Goldoni M, et al.
Genes (Basel)
. 2023 Dec;
14(12).
PMID: 38136979
Chromosomal submicroscopic imbalances represent well-known causes of neurodevelopmental disorders. In some cases, these can cause specific autosomal dominant syndromes, with high-to-complete penetrance and de novo occurrence of the variant. In...
13.
Azzara A, Cassano I, Lintas C, Bernardini L, Pilato F, Capone F, et al.
Eur J Neurol
. 2023 Oct;
31(1):e16088.
PMID: 37823721
Background: Facial palsy manifests as unilateral or bilateral weakness and inability to move some of the facial muscles. The aetiology may be different including idiopathic, trauma, infections or brain tumours...
14.
Melo U, Jatzlau J, Prada-Medina C, Flex E, Hartmann S, Ali S, et al.
Nat Commun
. 2023 Oct;
14(1):6301.
PMID: 37813867
No abstract available.
15.
Vivaldi C, Genovesi V, Ugolini C, Bernardini L, Casadei-Gardini A, Formica V, et al.
Oncology
. 2023 Sep;
102(2):157-167.
PMID: 37699372
Introduction: Mismatch repair (MMR) deficiency represents a biomarker and therapeutic target in various neoplasms, but its role in biliary tract cancers (BTCs) remains misunderstood. Methods: MMR status was retrospectively assessed...
16.
Ambrosetti I, Bernardini L, Pollazzon M, Giuffrida M, Guida V, Peluso F, et al.
Genes (Basel)
. 2023 Aug;
14(8).
PMID: 37628577
Split Hand-Foot Malformation (SHFM) is a congenital limb defect characterized by a median cleft of the hands and/or feet due to the absence/hypoplasia of the central rays. It may occur...
17.
Bouassida M, Egloff M, Levy J, Chatron N, Bernardini L, Guyader G, et al.
Eur J Hum Genet
. 2023 May;
31(8):895-904.
PMID: 37188826
Microduplications involving the MYT1L gene have mostly been described in series of patients with isolated schizophrenia. However, few reports have been published, and the phenotype has still not been well...
18.
Enhancer hijacking at the ARHGAP36 locus is associated with connective tissue to bone transformation
Melo U, Jatzlau J, Prada-Medina C, Flex E, Hartmann S, Ali S, et al.
Nat Commun
. 2023 Apr;
14(1):2034.
PMID: 37041138
Heterotopic ossification is a disorder caused by abnormal mineralization of soft tissues in which signaling pathways such as BMP, TGFβ and WNT are known key players in driving ectopic bone...
19.
Mastromoro G, Guadagnolo D, Novelli A, Torres B, Piane M, Magliozzi M, et al.
J Matern Fetal Neonatal Med
. 2023 Apr;
36(1):2201653.
PMID: 37041101
Laterality defects include morphological anomalies with impaired left-right asymmetry induction, such as dextrocardia, situs inversus abdominis, situs inversus totalis and situs ambiguus. The different arrangement of major organs is called...
20.
Fontana M, Fattori F, Trezzi S, Conte M, Bernardini L, Marando L, et al.
J Migr Health
. 2023 Mar;
7:100177.
PMID: 36968561
Background And Objective: The recent notable increase in refugees' flows, with refugee children and adolescents relocating worldwide, posed severe challenges to the different national healthcare systems. Social groups such as...