PRADELLA, LAURA MARIA
PRADELLA, LAURA MARIA
DIPARTIMENTO DI SCIENZE MEDICHE E CHIRURGICHE
Colorectal polyposis as a clue to the diagnosis of Cowden syndrome: Report of two cases and literature review
2021 Innella G.; Miccoli S.; Colussi D.; Pradella L.M.; Amato L.B.; Zuntini R.; Salfi N.C.M.; Collina G.; Ferrara F.; Ricciardiello L.; Turchetti D.
Detecting Variants in the NBN Gene While Testing for Hereditary Breast Cancer: What to Do Next?
2021 Zuntini, Roberta; Bonora, Elena; Pradella, Laura Maria; Amato, Laura Benedetta; Vidone, Michele; De Fanti, Sara; Catucci, Irene; Cortesi, Laura; Medici, Veronica; Ferrari, Simona; Gasparre, Giuseppe; Peterlongo, Paolo; Sazzini, Marco; Turchetti, Daniela
PTEN Hamartoma Tumor Syndrome: Skin Manifestations and Insights Into Their Molecular Pathogenesis
2021 Innella G.; Bonora E.; Neri I.; Virdi A.; Guglielmo A.; Pradella L.M.; Ceccarelli C.; Amato L.B.; Lanzoni A.; Miccoli S.; Gasparre G.; Zuntini R.; Turchetti D.
Where Birt-Hogg-Dubé meets Cowden Syndrome: Mirrored genetic defects in two cases of syndromic oncocytic tumours
2013 Pradella L.M.; Lang M.; Kurelac I.; Mariani E.; Guerra F.; Zuntini R.; Tallini G.; MacKay A.; Reis-Filho J.S.; Seri M.; Turchetti D.; Gasparre G.
Apolipoprotein B is a new target of the GDNF/RET and ET-3/EDNRB signalling pathways
2012 C. Evangelisti;F. Bianco;L. M. Pradella;A. Puliti;A. Goldoni;I. Sbrana;M. Rossi;M. Vargiolu;M. Seri;G. Romeo;V. Stanghellini;R. de Giorgio;E. Bonora
Two distinct thyroid tumours in a Cowden Syndrome patient carrying both a 10q23 and a mitochondrial DNA germline deletion
2011 Pradella LM; Zuntini R; Magini P; Ceccarelli C; Neri I; Cerasoli S; Graziano C; Gasparre G; Turchetti D
| Titolo | Autore(i) | Anno | Periodico | Editore | Tipo | File |
|---|---|---|---|---|---|---|
| Colorectal polyposis as a clue to the diagnosis of Cowden syndrome: Report of two cases and literature review | Innella G.; Miccoli S.; Colussi D.; Pradella L.M.; Amato L.B.; Zuntini R.; Salfi N.C.M.; Collina ...G.; Ferrara F.; Ricciardiello L.; Turchetti D. | 2021-01-01 | PATHOLOGY RESEARCH AND PRACTICE | - | 1.01 Articolo in rivista | - |
| Detecting Variants in the NBN Gene While Testing for Hereditary Breast Cancer: What to Do Next? | Zuntini, Roberta; Bonora, Elena; Pradella, Laura Maria; Amato, Laura Benedetta; Vidone, Michele; ...De Fanti, Sara; Catucci, Irene; Cortesi, Laura; Medici, Veronica; Ferrari, Simona; Gasparre, Giuseppe; Peterlongo, Paolo; Sazzini, Marco; Turchetti, Daniela | 2021-01-01 | INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES | - | 1.01 Articolo in rivista | IJMS - RZ.pdf; ijms-22-05832-s001.zip |
| PTEN Hamartoma Tumor Syndrome: Skin Manifestations and Insights Into Their Molecular Pathogenesis | Innella G.; Bonora E.; Neri I.; Virdi A.; Guglielmo A.; Pradella L.M.; Ceccarelli C.; Amato L.B.;... Lanzoni A.; Miccoli S.; Gasparre G.; Zuntini R.; Turchetti D. | 2021-01-01 | FRONTIERS IN MEDICINE | - | 1.01 Articolo in rivista | fmed-08-688105.pdf; Table_1.docx |
| Where Birt-Hogg-Dubé meets Cowden Syndrome: Mirrored genetic defects in two cases of syndromic oncocytic tumours | Pradella L.M.; Lang M.; Kurelac I.; Mariani E.; Guerra F.; Zuntini R.; Tallini G.; MacKay A.; Rei...s-Filho J.S.; Seri M.; Turchetti D.; Gasparre G. | 2013-01-01 | EUROPEAN JOURNAL OF HUMAN GENETICS | - | 1.01 Articolo in rivista | - |
| Apolipoprotein B is a new target of the GDNF/RET and ET-3/EDNRB signalling pathways | C. Evangelisti;F. Bianco;L. M. Pradella;A. Puliti;A. Goldoni;I. Sbrana;M. Rossi;M. Vargiolu;M. Se...ri;G. Romeo;V. Stanghellini;R. de Giorgio;E. Bonora | 2012-01-01 | NEUROGASTROENTEROLOGY AND MOTILITY | - | 1.01 Articolo in rivista | - |
| Two distinct thyroid tumours in a Cowden Syndrome patient carrying both a 10q23 and a mitochondrial DNA germline deletion | Pradella LM; Zuntini R; Magini P; Ceccarelli C; Neri I; Cerasoli S; Graziano C; Gasparre G; Turch...etti D | 2011-01-01 | JOURNAL OF MEDICAL GENETICS | - | 1.01 Articolo in rivista | - |