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1. [P4–069]: A PROSPECTIVE NEUROGENETIC STUDY ON EARLY‐ONSET DEMENTIA IN PATIENTS WITH UNCLEAR INITIAL DIAGNOSIS OF DEGENERATIVE DEMENTIA. (1st July 2017)

2. A functional gene expression analysis in epithelial sinonasal cancer: Biology and clinical relevance behind three histological subtypes. (March 2019)

3. A20 Reduced levels of the glucose transporter glut-1 in brain striatum and periphery reveals clues to specific pathomechanisms in childhood-onset Huntington disease. (12th September 2022)

5. AKT1 and BRAF mutations in pediatric aggressive fibromatosis. (8th April 2016)

6. Are Fusion Transcripts in Relapsed/Metastatic Head and Neck Cancer Patients Predictive of Response to Anti-EGFR Therapies?. (12th November 2017)

7. BRAF Mutation Analysis is a Valid Tool to Implement in Lynch Syndrome Diagnosis in Patients Classified According to the Bethesda Guidelines. Issue 3 (May 2014)

8. C11 Identifying loss-of-interruptions (LOI) in huntington disease families of Italian origin. (12th September 2022)

9. Capecitabine, oxaliplatin and irinotecan in combination, with bevacizumab (COI-B regimen) as first-line treatment of patients with advanced colorectal cancer. An Italian Trials of Medical Oncology phase II study. Issue 4 (March 2015)

10. Capecitabine, oxaliplatin and irinotecan in combination, with bevacizumab (COI-B regimen) as first-line treatment of patients with advanced colorectal cancer. An Italian Trials of Medical Oncology phase II study. Issue 4 (March 2015)