E. Bacchini
University of Parma
7 Papers
15 Citations
E. Bacchini is an academic researcher from University of Parma. The author has contributed to research in topics: Neurofibromatosis & Medicine. The author has an hindex of 6, co-authored 7 publications.
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Papers
Central nervous system atypical teratoid/rhabdoid tumour of infancy: CT And mr findings
Giulio Zuccoli,Giancarlo Izzi,E. Bacchini,Maria Teresa Tondelli,Francesco Ferrozzi,Massimo Bellomi +5 more
TL;DR: The clinical history and radiological findings in a child affected by central nervous system (CNS) ATRT and a new nomenclature was introduced, Atypical Teratoid/Rhabdoid Tumor of infancy and childhood.
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Mandibuloacral dysplasia type A in childhood
Livia Garavelli,Maria Rosaria D'Apice,Francesca Rivieri,M. Bertoli,Anita Wischmeijer,Chiara Gelmini,V. De Nigris,Enrico Albertini,Simonetta Rosato,Raffaele Virdis,E. Bacchini,R. Dal Zotto,Giacomo Banchini,Lorenzo Iughetti,S. Bernasconi,Andrea Superti-Furga,Giuseppe Novelli +16 more
TL;DR: The phenotype of MADA can be manifest in preschool age; diagnosis may be suggested by short and bulbous fingertips, facial features, and lipodystrophy, supported by the finding of acral osteolysis, and confirmed by mutation analysis.
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Noonan syndrome-like disorder with loose anagen hair: a second case with neuroblastoma
Livia Garavelli,Viviana Cordeddu,Stefania Errico,P Bertolini,Maria E. Street,Simonetta Rosato,Marzia Pollazzon,Anita Wischmeijer,Ivan Ivanovski,Paola Daniele,E. Bacchini,Alfonsa Anna Lombardi,Giancarlo Izzi,Giacomo Biasucci,Carmine Del Rossi,Domenico Corradi,Giovanni Cazzaniga,Carlo Dominici,Cesare Rossi,Alessandro De Luca,Sergio Bernasconi,Riccardo Riccardi,Eric Legius,Marco Tartaglia +23 more
TL;DR: Results do not support a major role of somatic SHOC2 mutations in these pediatric cancers, but this second instance of neuroblastoma in NSLAH suggests a possible predisposition to this malignancy in subjects heterozygous for the c.4A>G SH OC2 mutation.
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Magnetic resonance findings and ophthalmologic abnormalities are correlated in patients with neurofibromatosis type 1 (NF1)
M. Sigorini,Giulio Zuccoli,Francesco Ferrozzi,E. Bacchini,Maria E. Street,Paolo Piazza,Maurizio Rossi,Raffaele Virdis +7 more
TL;DR: It is concluded that a visual field evaluation is the most sensitive clinical test among those evaluated to predict the presence of optic pathway pathology on an MRI examination.
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•Journal Article
[Extracerebral neoplastic manifestations in neurofibromatosis 1: integrated diagnostic imaging].
TL;DR: The Schwannomas, which are a less common finding in NF-1, exhibited different features at MRI and CT, namely pseudo-liquid or solid-inhomogeneous patterns with irregular and inhomogeneous contrast enhancement relative to the Antoni A/B tumor component, while the plexiform neurofibromas had poorly-defined or infiltrating margins.
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