Marilina Nantron
Overview
Explore the profile of Marilina Nantron including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
10
Citations
118
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Ciceri S, Montalvao-de-Azevedo R, Tajbakhsh A, Bertolotti A, Spagnuolo R, Boschetti L, et al.
Cancer Gene Ther
. 2020 Dec;
28(9):1016-1024.
PMID: 33281191
Whereas 90% of patients with Wilms tumor (WT) reach cure, approximately half of patients developing a recurrent tumor die of the disease. Therefore, to disclose events leading to recurrence represents...
2.
Ciceri S, Gamba B, Corbetta P, Mondini P, Terenziani M, Catania S, et al.
Oncotarget
. 2018 Oct;
9(75):34079-34089.
PMID: 30344923
Wilms tumour (WT), the most frequent malignant childhood renal tumour, shows a high degree of genetic and epigenetic heterogeneity. Loss of imprinting on chromosome 11p15 is found in a large...
3.
Spreafico F, Biasoni D, Lo Vullo S, Gandola L, DAngelo P, Terenziani M, et al.
J Urol
. 2017 Jun;
198(5):1138-1145.
PMID: 28655531
Purpose: TW2003, the third Italian prospective study on Wilms tumor, aimed to improve survival in patients with stage III-IV tumors, de-escalate therapy for stage I-II nonanaplastic tumors, refine the risk...
4.
DAngelo P, Di Cataldo A, Terenziani M, Bisogno G, Collini P, Di Martino M, et al.
Pediatr Blood Cancer
. 2017 Jun;
64(12).
PMID: 28598537
Background: Children with Wilms' tumor (WT) aged under 24 months (infants) have a better prognosis than older patients. Our aim was to study the epidemiology of this age group, with...
5.
Suffia C, Sorrentino S, Vetrella S, Bifano D, Nantron M, De Bernardi B, et al.
Ital J Pediatr
. 2016 May;
42(1):52.
PMID: 27209026
Background: Five to 10 % of children with neuroblastoma present with symptoms of epidural compression (EC). More than half these patients are diagnosed in the first year of life. The...
6.
Astolfi A, Melchionda F, Perotti D, Fois M, Indio V, Urbini M, et al.
Oncotarget
. 2015 Oct;
6(38):40934-9.
PMID: 26516930
Purpose: Clear cell sarcoma of the kidney (CCSK) is a rare pediatric renal tumor that is frequently difficult to distinguish among other childhood renal tumors due to its histological heterogeneity....
7.
Spreafico F, Gamba B, Mariani L, Collini P, DAngelo P, Pession A, et al.
J Urol
. 2012 Nov;
189(1):260-6.
PMID: 23174227
Purpose: The specific aims of the AIEOP-TW-2003 protocol included prospectively investigating a possible association of tumor loss of heterozygosity with outcomes in children treated for Wilms tumor. Materials And Methods:...
8.
Perotti D, Spreafico F, Torri F, Gamba B, dAdamo P, Pizzamiglio S, et al.
Genes Chromosomes Cancer
. 2012 Mar;
51(7):644-53.
PMID: 22407497
Despite the excellent survival rate of Wilms tumor (WT) patients, only approximately one-half of children who suffer tumor recurrence reach second durable remission. This underlines the need for novel markers...
9.
Spreafico F, Gandola L, DAngelo P, Terenziani M, Collini P, Bianchi M, et al.
Int J Radiat Oncol Biol Phys
. 2010 Nov;
82(1):348-54.
PMID: 21075548
Purpose: We analyzed whether the prognosis can differ among Wilms tumors (WT) labeled as Stage III according to currently adopted classification systems. Methods And Materials: Patients with nonanaplastic Stage III...
10.
Castagnola E, Battaglia T, Bandettini R, Caviglia I, Baldelli I, Nantron M, et al.
Support Care Cancer
. 2008 Sep;
17(3):321-4.
PMID: 18802726
Goals Of Work: The goal of this study was to describe the incidence of Clostridium difficile-associated disease (CDAD) in children with solid tumours. Patients And Methods: After documentation of a...