• 427 Citations
  • 11 h-Index
19962019
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Fingerprint Dive into the research topics where Roberto Cocchi is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 5 Similar Profiles
Squamous Cell Carcinoma Medicine & Life Sciences
Free Tissue Flaps Medicine & Life Sciences
Salivary Glands Medicine & Life Sciences
Neck Medicine & Life Sciences
Minor Salivary Glands Medicine & Life Sciences
Bone and Bones Medicine & Life Sciences
Neoplasms Medicine & Life Sciences
Neoplasm Metastasis Medicine & Life Sciences

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Research Output 1996 2019

  • 427 Citations
  • 11 h-Index
  • 30 Article

Reconstruction of Full-Thickness Defects of the Lower Lip With a Double Overlying Cervical Flap

Copelli, C., Manfuso, A., Pederneschi, N., Hanna, K. T., Cassano, L. & Cocchi, R., Jul 1 2019, In : The Journal of craniofacial surgery. 30, 5, p. e428-e430

Research output: Contribution to journalArticle

Lip
Free Tissue Flaps
Operative Time
Compliance
Cicatrix
5 Citations (Scopus)

Gestione del fallimento dei lembi liberi in chirurgia testa-collo

Translated title of the contribution: Management of free flap failure in head and neck surgeryCopelli, C., Tewfik, K., Cassano, L., Pederneschi, N., Catanzaro, S., Manfuso, A. & Cocchi, R., Oct 1 2017, In : Acta Otorhinolaryngologica Italica. 37, 5, p. 387-392 6 p.

Research output: Contribution to journalArticle

Free Tissue Flaps
Neck
Head
Necrosis
Hospital Units
5 Citations (Scopus)

Management of free flap failure in head and neck surgery

Copelli, C., Tewfik, K., Cassano, L., Pederneschi, N., Catanzaro, S., Manfuso, A. & Cocchi, R., Oct 2017, In : Acta Otorhinolaryngologica Italica. 37, 5, p. 387-392 6 p.

Research output: Contribution to journalArticle

Free Tissue Flaps
Neck
Head
Necrosis
Hospital Units
2 Citations (Scopus)

MEN1 gene mutation with parathyroid carcinoma: First report of a familial case

Cinque, L., Sparaneo, A., Salcuni, A. S., De Martino, D., Battista, C., Logoluso, F., Palumbo, O., Cocchi, R., Maiello, E., Graziano, P., Hendy, G. N., Cole, D. E. C., Scillitani, A. & Guarnieri, V., Nov 1 2017, In : Endocrine Connections. 6, 8, p. 886-891 6 p.

Research output: Contribution to journalArticle

Multiple Endocrine Neoplasia Type 1
Parathyroid Neoplasms
Mutation
Genes
Missense Mutation
2 Citations (Scopus)

Putative TMPRSS3/GJB2 digenic inheritance of hearing loss detected by targeted resequencing

Leone, M. P., Palumbo, P., Ortore, R., Castellana, S., Palumbo, O., Melchionda, S., Palladino, T., Stallone, R., Mazza, T., Cocchi, R. & Carella, M., Jun 1 2017, In : Molecular and Cellular Probes. 33, p. 24-27 4 p.

Research output: Contribution to journalArticle

Hearing Loss
Deafness
Genes