Alessandro Raso
Alessandro Raso
Asl 3, S.C. Patologia Clinica
Verified email at asl3.liguria.it
TitleCited byYear
Reduced folate carrier polymorphism (80A→ G) and neural tube defects
P De Marco, MG Calevo, A Moroni, E Merello, A Raso, RH Finnell, H Zhu, ...
European journal of human genetics 11 (3), 245, 2003
1002003
Evaluation of a methylenetetrahydrofolate-dehydrogenase 1958G> A polymorphism for neural tube defect risk
P De Marco, E Merello, MG Calevo, S Mascelli, A Raso, A Cama, V Capra
Journal of human genetics 51 (2), 98-103, 2006
862006
Both CD133+ and CD133 medulloblastoma cell lines express ligands for triggering NK receptors and are susceptible to NK‐mediated cytotoxicity
R Castriconi, A Dondero, F Negri, F Bellora, P Nozza, B Carnemolla, ...
European journal of immunology 37 (11), 3190-3196, 2007
612007
Therapeutic and prognostic implications of BRAF V600E in pediatric low-grade gliomas
A Lassaletta, M Zapotocky, M Mistry, V Ramaswamy, M Honnorat, ...
Journal of Clinical Oncology 35 (25), 2934, 2017
552017
Predictability, efficacy and safety of radiosensitization of glioblastoma‐initiating cells by the ATM inhibitor KU‐60019
D Vecchio, A Daga, E Carra, D Marubbi, G Baio, CE Neumaier, S Vagge, ...
International journal of cancer 135 (2), 479-491, 2014
372014
Pharmacokinetics, pharmacodynamics and efficacy on pediatric tumors of the glioma radiosensitizer KU 60019
D Vecchio, A Daga, E Carra, D Marubbi, A Raso, S Mascelli, P Nozza, ...
International journal of cancer 136 (6), 1445-1457, 2015
312015
High levels of PROM1 (CD133) transcript are a potential predictor of poor prognosis in medulloblastoma
A Raso, S Mascelli, R Biassoni, P Nozza, M Kool, A Pistorio, E Ugolotti, ...
Neuro-oncology 13 (5), 500-508, 2011
292011
Diagnostic and prognostic value of 18F-DOPA PET and 1H-MR spectroscopy in pediatric supratentorial infiltrative gliomas: a comparative study
G Morana, A Piccardo, M Puntoni, P Nozza, A Cama, A Raso, S Mascelli, ...
Neuro-oncology 17 (12), 1637-1647, 2015
272015
Characterization of Glioma Stem Cells Through Multiple Stem Cell Markers and Their Specific Sensitization to Double‐Strand Break‐Inducing Agents by Pharmacological Inhibitioná…
A Raso, D Vecchio, E Cappelli, M Ropolo, A Poggi, P Nozza, R Biassoni, ...
Brain Pathology 22 (5), 677-688, 2012
272012
Identification of novel chromosomal abnormalities and prognostic cytogenetics markers in intracranial pediatric ependymoma
A Pezzolo, V Capra, A Raso, F Morandi, F Parodi, C Gambini, P Nozza, ...
Cancer letters 261 (2), 235-243, 2008
272008
HLXB9 homeobox gene and caudal regression syndrome
E Merello, P De Marco, S Mascelli, A Raso, MG Calevo, M Torre, A Cama, ...
Birth Defects Research Part A: Clinical and Molecular Teratology 76 (3), 205-209, 2006
232006
SMARCB1/INI1 Involvement in Pediatric Chordoma
M Antonelli, A Raso, S Mascelli, M Gessi, P Nozza, A Coli, MP Gardiman, ...
The American journal of surgical pathology 41 (1), 56-61, 2017
212017
Successful isolation and long‐term establishment of a cell line with stem cell‐like features from an anaplastic medulloblastoma
A Raso, F Negri, A Gregorio, P Nozza, S Mascelli, P De Marco, E Merello, ...
Neuropathology and applied neurobiology 34 (3), 306-315, 2008
212008
Quantitative Real-Time PCR
R Biassoni, A Raso
Humana, 2016
202016
Cervico‐medullary desmoplastic infantile ganglioglioma: An unusual case with diffuse leptomeningeal dissemination at diagnosis
C Milanaccio, P Nozza, M Ravegnani, A Rossi, A Raso, C Gambini, ...
Pediatric blood & cancer 45 (7), 986-990, 2005
202005
Whole-genome sequencing as standard practice for the analysis of clonality in outbreaks of meticillin-resistant Staphylococcus aureus in a paediatric setting
E Ugolotti, P Larghero, I Vanni, R Bandettini, G Tripodi, G Melioli, ...
Journal of Hospital Infection 93 (4), 375-381, 2016
182016
Mutational screening of the CYP26A1 gene in patients with caudal regression syndrome
P De Marco, E Merello, S Mascelli, A Raso, A Santamaria, C Ottaviano, ...
Birth Defects Research Part A: Clinical and Molecular Teratology 76 (2), 86-95, 2006
172006
Expanding the mutational spectrum associated to neural tube defects: Literature revision and description of novel VANGL1 mutations
E Merello, S Mascelli, A Raso, G Piatelli, A Consales, A Cama, Z Kibar, ...
Birth Defects Research Part A: Clinical and Molecular Teratology 103 (1), 51-61, 2015
162015
Rhabdoid meningioma of the tentorium with expression of desmin in a 12-year-old Turner syndrome patient
P Nozza, A Raso, A Rossi, C Milanaccio, A Pezzolo, V Capra, C Gambini, ...
Acta neuropathologica 110 (2), 205-206, 2005
162005
Grading and outcome prediction of pediatric diffuse astrocytic tumors with diffusion and arterial spin labeling perfusion MRI in comparison with 18F–DOPA PET
G Morana, A Piccardo, D Tortora, M Puntoni, M Severino, P Nozza, ...
European journal of nuclear medicine and molecular imaging 44 (12), 2084-2093, 2017
152017
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