Author/Creator: Riva, P - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Riva, P

1. 471 POTENTIAL ROLE OF NEOADJUVANT RADIO-CHEMOTHERAPY ON NEW-ONSET ATRIAL FIBRILLATION AFTER HYBRID IVOR-LEWIS ESOPHAGECTOMY FOR CANCER. (14th September 2020)

Authors:: Pansa, A; Riva, P; Da Roit, A; Basato, S; Ricchitelli, S; Luberto, A; Marano, S; Castoro, C
Journal:: Diseases of the esophagus
Issue:: Volume 33(2020)Supplement 1
Page Start:
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

2. 605 STEPWISE APPROACH TO ROBOTIC SURGERY IN A HIGH-VOLUME CENTER WITHOUT PREVIOUS EXPERIENCE IN ROBOTIC ESOPHAGEAL SURGERY. (14th September 2020)

Authors:: Riva, P; Pansa, A; Da Roit, A; Basato, S; Marano, S; Castoro, C
Journal:: Diseases of the esophagus
Issue:: Volume 33(2020)Supplement 1
Page Start:
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

3. Duplications in addition to terminal deletions are present in a proportion of ring chromosomes: clues to the mechanisms of formation. Issue 3 (15th November 2007)

Authors:: Rossi, E; Riegel, M; Messa, J; Gimelli, S; Maraschio, P; Ciccone, R; Stroppi, M; Riva, P; Perrotta, C S; Mattina, T; Memo, L; Baumer, A; Kucinskas, V; Castellan, C; Schinzel, A; Zuffardi, O
Journal:: Journal of medical genetics
Issue:: Volume 45:Issue 3(2008)
Page Start:: 147
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

4. Interstitial telomeres of an inv(9)(p11.2;q34) involved in a jumping translocation found in a woman through a stable unbalanced translocation in her malformed child. Issue 8 (1st August 2002)

Authors:: Sala, E; Villa, N; Riva, P; Varisco, T; Larizza, L; Dalprà, L
Journal:: Journal of medical genetics
Issue:: Volume 39:Issue 8(2002)
Page Start:: e42
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

5. Mental retardation and cardiovascular malformations in NF1 microdeleted patients point to candidate genes in 17q11.2. Issue 1 (16th January 2004)

Authors:: Venturin, M; Guarnieri, P; Natacci, F; Stabile, M; Tenconi, R; Clementi, M; Hernandez, C; Thompson, P; Upadhyaya, M; Larizza, L; Riva, P
Journal:: Journal of medical genetics
Issue:: Volume 41:Issue 1(2004)
Page Start:: 35
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗