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Research Output 1999 2017

  • 3919 Citations
  • 10 h-Index
  • 15 Article
2017
3 Citations (Scopus)

Mechanism of action of trabectedin in desmoplastic small round cell tumor cells

Uboldi, S., Craparotta, I., Colella, G., Ronchetti, E., Beltrame, L., Vicario, S., Marchini, S., Panini, N., Dagrada, G., Bozzi, F., Pilotti, S., Galmarini, C. M., D'Incalci, M. & Gatta, R., Feb 6 2017, In : BMC Cancer. 17, 1, p. 107

Research output: Contribution to journalArticle

trabectedin
Desmoplastic Small Round Cell Tumor
Sarcoma
Pharmaceutical Preparations
Cell Line
3 Citations (Scopus)

Mechanism of action of trabectedin in desmoplastic small round cell tumor cells

Uboldi, S., Craparotta, I., Colella, G., Ronchetti, E., Beltrame, L., Vicario, S., Marchini, S., Panini, N., Dagrada, G., Bozzi, F., Pilotti, S., Galmarini, C. M., D'Incalci, M. & Gatta, R., Feb 6 2017, In : BMC Cancer. 17, 1, 107.

Research output: Contribution to journalArticle

trabectedin
Desmoplastic Small Round Cell Tumor
Sarcoma
Pharmaceutical Preparations
Cell Line
3 Citations (Scopus)

Mechanism of action of trabectedin in desmoplastic small round cell tumor cells.

Uboldi, S., Craparotta, I., Colella, G., Ronchetti, E., Beltrame, L., Vicario, S., Marchini, S., Panini, N., Dagrada, G., Bozzi, F., Pilotti, S., Galmarini, C. M., D'Incalci, M. & Gatta, R., Feb 1 2017, In : BMC Cancer. 17, 1, p. 107 1 p.

Research output: Contribution to journalArticle

2015
20 Citations (Scopus)

Profiling cancer gene mutations in longitudinal epithelial ovarian cancer biopsies by targeted next-generation sequencing: A retrospective study

Beltrame, L., Di Marino, M., Fruscio, R., Calura, E., Chapman, B., Clivio, L., Sina, F., Mele, C., Iatropoulos, P., Grassi, T., Fotia, V., Romualdi, C., Martini, P., Noris, M., Paracchini, L., Craparotta, I., Petrillo, M., Milani, R., Perego, P., Ravaggi, A. & 4 others, Zambelli, A., Ronchetti, E., D'Incalci, M. & Marchini, S., Jul 1 2015, In : Annals of Oncology. 26, 7, p. 1363-1371 9 p.

Research output: Contribution to journalArticle

Neoplasm Genes
Retrospective Studies
Biopsy
Mutation
Homologous Recombination
2005
463 Citations (Scopus)

A novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 gene

Priori, S. G., Pandit, S. V., Rivolta, I., Berenfeld, O., Ronchetti, E., Dhamoon, A., Napolitano, C., Anumonwo, J., Di Barletta, M. R., Gudapakkam, S., Bosi, G., Stramba-Badiale, M. & Jalife, J., Apr 15 2005, In : Circulation Research. 96, 7, p. 800-807 8 p.

Research output: Contribution to journalArticle

Cardiac Arrhythmias
Mutation
Genes
Electrocardiography
Phenotype
326 Citations (Scopus)
Long QT Syndrome
Genetic Testing
Mutation
Codon
Genetic Loci
2004
472 Citations (Scopus)

Association of long QT syndrome loci and cardiac events among patients treated with β-blockers

Priori, S. G., Napolitano, C., Schwartz, P. J., Grillo, M., Bloise, R., Ronchetti, E., Moncalvo, C., Tulipani, C., Veia, A., Bottelli, G. & Nastoli, J., Sep 15 2004, In : Journal of the American Medical Association. 292, 11, p. 1341-1344 4 p.

Research output: Contribution to journalArticle

Long QT Syndrome
Torsades de Pointes
Sudden Cardiac Death
Syncope
Ventricular Tachycardia
2003
1036 Citations (Scopus)

Risk stratification in the long-QT syndrome

Priori, S. G., Schwartz, P. J., Napolitano, C., Bloise, R., Ronchetti, E., Grillo, M., Vicentini, A., Spazzolini, C., Nastoli, J., Bottelli, G., Folli, R. & Cappelletti, D., May 8 2003, In : New England Journal of Medicine. 348, 19, p. 1866-1874 9 p.

Research output: Contribution to journalArticle

Long QT Syndrome
Mutation
Genotype
KCNQ1 Potassium Channel
Sodium Channels
2002
822 Citations (Scopus)

Natural history of Brugada syndrome: Insights for risk stratification and management

Priori, S. G., Napolitano, C., Gasparini, M., Pappone, C., Della Bella, P., Giordano, U., Bloise, R., Giustetto, C., De Nardis, R., Grillo, M., Ronchetti, E., Faggiano, G. & Nastoli, J., Mar 19 2002, In : Circulation. 105, 11, p. 1342-1347 6 p.

Research output: Contribution to journalArticle

Brugada Syndrome
Risk Management
Electric Stimulation
Sudden Death
Heart Arrest
2001
142 Citations (Scopus)

Molecular diagnosis in a child with sudden infant death syndrome

Schwartz, P. J., Priori, S. G., Bloise, R., Napolitano, C., Ronchetti, E., Piccinini, A., Goj, C., Breithardt, G., Schulze-Bahr, E., Wedekind, H. & Nastoli, J., Oct 20 2001, In : Lancet. 358, 9290, p. 1342-1343 2 p.

Research output: Contribution to journalArticle

Long QT Syndrome
Sudden Infant Death
Neonatal Screening
Mutation
Inborn Genetic Diseases
2000
267 Citations (Scopus)

Evidence for a cardiac ion channel mutation underlying drug-induced QT prolongation and life-threatening arrhythmias

Napolitano, C., Schwartz, P. J., Brown, A. M., Ronchetti, E., Bianchi, L., Pinnavaia, A., Acquaro, G. & Priori, S. G., 2000, In : Journal of Cardiovascular Electrophysiology. 11, 6, p. 691-696 6 p.

Research output: Contribution to journalArticle

Life Support Care
Ion Channels
Cardiac Arrhythmias
Long QT Syndrome
Mutation
2 Citations (Scopus)

Gene specific therapy for arrhythmogenic disorders.

Priori, S. G., Ronchetti, E. & Memmi, M., Sep 2000, In : Italian Heart Journal. 1 Suppl 3

Research output: Contribution to journalArticle

219 Citations (Scopus)
Flecainide
Brugada Syndrome
Long QT Syndrome
Sodium Channels
Safety
1999
141 Citations (Scopus)

Cellular dysfunction of LQT5-minK mutants: Abnormalities of I(Ks), I(Kr) and trafficking in long QT syndrome

Bianchi, L., Shen, Z., Dennis, A. T., Priori, S. G., Napolitano, C., Ronchetti, E., Bryskin, R., Schwartz, P. J. & Brown, A. M., 1999, In : Human Molecular Genetics. 8, 8, p. 1499-1507 9 p.

Research output: Contribution to journalArticle

Mink
Long QT Syndrome
Mutation
HEK293 Cells
Xenopus