Lucia Quaglietta
Overview
Explore the profile of Lucia Quaglietta including associated specialties, affiliations and a list of published articles.
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Articles
46
Citations
449
Followers
0
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Recent Articles
1.
Mirone G, Picariello S, Russo C, Cicala D, Spennato P, Onorini N, et al.
J Neurosurg Sci
. 2025 Mar;
PMID: 40047450
Background: Complete microsurgical removal of pediatric brain tumors remains a significant prognostic factor, but it is still associated with a significant degree of morbidity and mortality. Magnetic resonance-guided laser interstitial...
2.
De Martino L, Mirabelli P, Quaglietta L, Ferrara U, Picariello S, De Gennaro D, et al.
Childs Nerv Syst
. 2024 Sep;
40(11):3701.
PMID: 39311931
No abstract available.
3.
Russo C, Aliberti F, Ferrara U, Russo C, De Gennaro D, Cristofano A, et al.
Diagnostics (Basel)
. 2024 Sep;
14(17).
PMID: 39272627
Craniosynostoses (CRS) are caused by the premature fusion of one or more cranial sutures, with isolated nonsyndromic CRS accounting for most of the clinical manifestations. Such premature suture fusion impacts...
4.
De Martino L, Mirabelli P, Quaglietta L, Ferrara U, Picariello S, De Gennaro D, et al.
Childs Nerv Syst
. 2024 Aug;
40(11):3693-3700.
PMID: 39133244
Purpose: Craniosynostosis (CRS) is a rare congenital cranial malformation in which 1 or more cranial or facial sutures are fused in utero or rapidly fused in early infancy. The cranial...
5.
Mastronuzzi A, Quaglietta L, Schiavello E, Carai A
Front Mol Neurosci
. 2024 May;
17:1423298.
PMID: 38779356
No abstract available.
6.
De Martino L, Russo C, Bifano D, Quaglietta L, Spennato P, Cinalli G
Childs Nerv Syst
. 2024 Apr;
40(8):2619-2623.
PMID: 38689102
Pallister-Killian syndrome (PKS; OMIM #601803) is a rare genetic disorder typically characterized by developmental delay, seizures, sparse temporal hair, and facial dysmorphisms. PKS is most frequently caused by mosaic supernumerary...
7.
Bibbo F, Asadzadeh F, Boccia A, Sorice C, Bianco O, Sacca C, et al.
Int J Mol Sci
. 2024 Apr;
25(7).
PMID: 38612726
Medulloblastoma (MB) is a highly malignant childhood brain tumor. Group 3 MB (Gr3 MB) is considered to have the most metastatic potential, and tailored therapies for Gr3 MB are currently...
8.
Ewijk R, Chatziantoniou C, Adams M, Bertolini P, Bisogno G, Bouhamama A, et al.
Pediatr Radiol
. 2023 Sep;
53(12):2539-2551.
PMID: 37682330
Objective: To investigate the feasibility of diffusion-weighted magnetic resonance imaging (DW-MRI) as a predictive imaging marker after neoadjuvant chemotherapy in patients with rhabdomyosarcoma. Material And Methods: We performed a multicenter...
9.
De Martino L, Picariello S, Russo C, Errico M, Spennato P, Papa M, et al.
Front Mol Neurosci
. 2023 Aug;
16:1152430.
PMID: 37547920
Introduction: Pediatric diffuse midline gliomas (DMG), H3 K27- altered, are the most aggressive pediatric central nervous system (CNS) malignancies. Disease outcome is dismal with a median survival of less than...
10.
Spinelli C, Ghionzoli M, Sahli L, Guglielmo C, Frascella S, Romano S, et al.
Cancers (Basel)
. 2023 Jul;
15(14).
PMID: 37509342
DICER1 syndrome is a rare genetic disorder that predisposes patients to the development of malignant and non-malignant diseases. Presently, DICER1 syndrome diagnosis still occurs late, usually following surgical operations, affecting...