Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Eugenio Maria Covelli"'
Autor:
Maria Grazia Pionelli, Federica Mazio, Maria Elena Errico, Carmela Russo, Adriana Cristofano, Eugenio Maria Covelli, Vittoria Donofrio, Maria Capasso, Michele Antonio Capozza, Fabiola De Gregorio, Serena Ruotolo, Massimo Eraldo Abate, Giuseppe Cinalli
Publikováno v:
Frontiers in Oncology, Vol 14 (2024)
The development of cerebral cavernous malformations (CCMs) is a well-recognized sequela of irradiation to the brain in pediatric tumors, particularly in medulloblastoma, glioma, and acute lymphoblastic leukaemia. So far, only one case of cerebral cav
Externí odkaz:
https://doaj.org/article/1ce557d22502431a8cc48c0e438fac2a
Autor:
Camilla Russo, Ferdinando Aliberti, Ursula Pia Ferrara, Carmela Russo, Domenico Vincenzo De Gennaro, Adriana Cristofano, Anna Nastro, Domenico Cicala, Pietro Spennato, Mario Quarantelli, Marco Aiello, Andrea Soricelli, Giovanni Smaldone, Nicola Onorini, Lucia De Martino, Stefania Picariello, Stefano Parlato, Peppino Mirabelli, Lucia Quaglietta, Eugenio Maria Covelli, Giuseppe Cinalli
Publikováno v:
Diagnostics, Vol 14, Iss 17, p 1842 (2024)
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 both skull and brain morphology and invo
Externí odkaz:
https://doaj.org/article/912fa28d8125413c9b22943c681b4721
Autor:
Federica Mazio, Giuseppina Aloj, Grazia Maria Giovanna Pastorino, Teresa Perillo, Carmela Russo, Maria Pia Riccio, Eugenio Maria Covelli, Rosanna Parasole, Enrico Tedeschi, Lorenzo Ugga, Alessandra D’Amico, Mario Quarantelli
Publikováno v:
Biology, Vol 11, Iss 4, p 499 (2022)
Whether chemotherapy (ChT) and radiotherapy (RT) determine neurocognitive impairment in acute lymphoblastic leukemia long-term survivors (ALL LTSs) through similar mechanisms affecting the same brain regions is still unknown. We compared neurocogniti
Externí odkaz:
https://doaj.org/article/7ca118ebf7e5492088583cc8bd4ce9c6
Autor:
Eugenio Maria Covelli, Ferdinando Aliberti, Giuliana Di Martino, Anna Nastro, Claudio Ruggiero, Giuseppe Cinalli, Pietro Spennato, Daniele Cascone, Federica Mazio, Carmela Russo, Giuseppe Mirone
Publikováno v:
Child's Nervous System
PurposeTo evaluate the anatomical variations of dural venous sinuses in children with external hydrocephalus, proposing a radiological grading of progressive anatomic restriction to venous outflow based on brain phase-contrast magnetic resonance veno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ece9560982d62c04864c2f5e583103d3
https://doi.org/10.1007/s00381-021-05322-5
https://doi.org/10.1007/s00381-021-05322-5
Autor:
Francesco Rolando, Alessandra Alfieri, Pasqualino de Marinis, Luigi Manfredonia, Alberto de Bellis, Pasquale Orabona, Sara Bruscella, Eugenio Maria Covelli
Publikováno v:
World Neurosurgery. 145:370-375
Background Primary central nervous system sarcomas are rare primitive mesenchymal non-meningothelial tumors. Malignant peripheral nerve sheath tumor accounts for 5% of sarcomas, with an incidence of approximately 0.001% and a recognized association w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::591f099ca06fbeb5bbcc72ce3b9f8353
https://doi.org/10.1016/j.wneu.2020.08.148
https://doi.org/10.1016/j.wneu.2020.08.148
Autor:
Anna Nastro, Maria De Liso, Domenico Cicala, Eugenio Maria Covelli, Giuseppe Cinalli, Camilla Russo
Publikováno v:
Child's Nervous System. 36:2497-2509
Tuberous sclerosis complex (TSC) is a rare autosomal dominant disorder affecting multiple systems, due to inactivating mutations of TSC1 or TSC2 mTOR pathway genes. Neurological manifestations are observed in about 95% cases, representing the most fr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::368bd8e08172b9c090bbf72bc20c24b7
https://doi.org/10.1007/s00381-020-04705-4
https://doi.org/10.1007/s00381-020-04705-4
Autor:
Carmela Russo, Maria Agnese Pirozzi, Federica Mazio, Daniele Cascone, Domenico Cicala, Maria De Liso, Anna Nastro, Eugenio Maria Covelli, Giuseppe Cinalli, Mario Quarantelli
Publikováno v:
SSRN Electronic Journal.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce53c37ec1bb6eb7513509057185dbf9
https://doi.org/10.2139/ssrn.4095678
https://doi.org/10.2139/ssrn.4095678
Autor:
Antonio Della Volpe, Paola Festa, Alfonso Maria Varricchio, Carmela Russo, Eugenio Maria Covelli, Delfina Bifano, Piera Piroli, Antonietta De Lucia, Arianna Di Stadio, Franco Ionna
Publikováno v:
Healthcare. 10:1962
Nodular fasciitis (NF) is a benign fibroblastic and myofibroblastic proliferation of subcutaneous tissues. Rarely, it has been identified in the ear and more rarely in children. We describe a case in a four-year-old girl and the surgical management o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f56315b3ee17c2c12ecb74903065a4c3
https://doi.org/10.3390/healthcare10101962
https://doi.org/10.3390/healthcare10101962
Autor:
Carmela Russo, Daniele Cascone, Camilla Russo, Eugenio Maria Covelli, Federica Mazio, Giuseppe Cinalli, Claudia Santoro
Publikováno v:
Cancers, Vol 13, Iss 1831, p 1831 (2021)
Cancers
Cancers
Simple Summary Central nervous system involvement (CNS) is a common finding in Neurofibromatosis type 1 (NF1). Beside tumor-related manifestations, NF1 is also characterized by a wide spectrum of CNS alterations with variable impacts on functioning a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b5bb4fdf5aaf730152f182d450b32f5
https://www.mdpi.com/2072-6694/13/8/1831
https://www.mdpi.com/2072-6694/13/8/1831
Autor:
Camilla, Russo, Anna, Nastro, Domenico, Cicala, Maria, De Liso, Eugenio Maria, Covelli, Giuseppe, Cinalli
Publikováno v:
Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery. 36(10)
Tuberous sclerosis complex (TSC) is a rare autosomal dominant disorder affecting multiple systems, due to inactivating mutations of TSC1 or TSC2 mTOR pathway genes. Neurological manifestations are observed in about 95% cases, representing the most fr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cbda45f7a4884906466a2100a9468763
https://pubmed.ncbi.nlm.nih.gov/32519125
https://pubmed.ncbi.nlm.nih.gov/32519125