INNELLA, GIOVANNI
INNELLA, GIOVANNI
DIPARTIMENTO DI SCIENZE MEDICHE E CHIRURGICHE
Assegnisti
Cancer prognosis and treatment results in patients with PTEN Hamartoma Tumour Syndrome (PHTS)-a European cohort study
2025 Hendricks, Linda A J; Verbeek, Katja C J; Schuurs-Hoeijmakers, Janneke H M; De Putter, Robin; Brems, Hilde; Van Daele, Sien H; Anastasiadou, Violetta C; Foretová, Lenka; Benusiglio, Patrick R; Gerasimenko, Anna; Colas, Chrystelle; Villy, Marie-Charlotte; Houdayer, Claude; Branchaud, Maud; Hüneburg, Robert; Aretz, Stefan; Jahn, Arne; Steinke-Lange, Verena; Innella, Giovanni; Turchetti, Daniela; Barili, Valeria; Genuardi, Maurizio; Panfili, Arianna; Baldassarri, Margherita; Irmejs, Arvīds; De Jong, Mirjam M; Links, Thera P; Leter, Edward M; Bosch, Daniëlle G M; Donze, Stephany H; Van Der Post, Rachel S; Mensenkamp, Arjen R; Westdorp, Harm; Høberg-Vetti, Hildegunn; Tveit Haavind, Marianne; Jørgensen, Kjersti; Mæhle, Lovise; Briskemyr, Siri; Garcia, Juliette Dupont; Blatnik, Ana; Balmaña, Judith; Torres, Maite; Brunet, Joan; Lleuger-Pujol, Roser; Tham, Emma; Tischkowitz, Marc; Evans, D Gareth; Hyder, Zerin; Hoogerbrugge, Nicoline; Vos, Janet R
Clinical genetic services in the Emilia-Romagna region, Italy: current activity and open issues: a mixed-method study
2025 Godino, Lea; Ambrosini, Enrico; Barili, Valeria; Graziano, Claudio; Garavelli, Livia; Calabrese, Olga; Neri, Marcella; Sangiorgi, Luca; Bertonazzi, Benedetta; Innella, Giovanni; Turchetti, Daniela; Percesepe, Antonio
The risk of a second primary cancer in PTEN Hamartoma Tumor Syndrome (PHTS)
2025 Hendricks, Linda A J; Verbeek, Katja C J; Schuurs-Hoeijmakers, Janneke H M; De Jong, Mirjam M; Links, Thera P; Brems, Hilde; Aerden, Mio; Brunet, Joan; Lleuger-Pujol, Roser; Hüneburg, Robert; Aretz, Stefan; Colas, Chrystelle; Villy, Marie-Charlotte; Woodward, Emma R; Evans, D Gareth; Bosch, Daniëlle G M; Donze, Stephany H; Foretová, Lenka; Blatnik, Ana; Leter, Edward M; Tischkowitz, Marc; Jahn, Arne; De Putter, Robin; Dupont, Juliette; Briskemyr, Siri; Steinke-Lange, Verena; Baldassarri, Margherita; Anastasiadou, Violetta C; Irmejs, Arvīds; Oliveira, Carla; Van Der Post, Rachel S; Mensenkamp, Arjen R; Tesi, Bianca; Mu, Ninni; Benusiglio, Patrick R; Gerasimenko, Anna; Innella, Giovanni; Turchetti, Daniela; Houdayer, Claude; Branchaud, Maud; Høberg-Vetti, Hildegunn; Haavind, Marianne Tveit; Balmaña, Judith; Torres, Maite; Genuardi, Maurizio; Panfili, Arianna; Jørgensen, Kjersti; Mæhle, Lovise; Hoogerbrugge, Nicoline; Vos, Janet R
Atypical cancer risk profile in carriers of Italian founder BRCA1 variant p.His1673del: Implications for classification and clinical management
2024 Innella, Giovanni; Fortuno, Cristina; Caleca, Laura; Feng, Bing-Jian; Carroll, Courtney; Parsons, Michael T; Miccoli, Sara; Montagna, Marco; Calistri, Daniele; Cortesi, Laura; Pasini, Barbara; Manoukian, Siranoush; Giachino, Daniela; Matricardi, Laura; Foti, Maria Cristina; Zampiga, Valentina; Piombino, Claudia; Barbieri, Elena; Lutati, Francesca Vignolo; Azzolini, Jacopo; Danesi, Rita; Arcangeli, Valentina; Caputo, Sandrine M; Boutry-Kryza, Nadia; Goussot, Vincent; Hiraki, Susan; Richardson, Marcy; Ferrari, Simona; Radice, Paolo; Spurdle, Amanda B; Turchetti, Daniela
Cancer Risks Associated With TP53 Pathogenic Variants: Maximum Likelihood Analysis of Extended Pedigrees for Diagnosis of First Cancers Beyond the Li-Fraumeni Syndrome Spectrum
2024 Fortuno, Cristina; Feng, Bing-Jian; Carroll, Courtney; Innella, Giovanni; Kohlmann, Wendy; Lázaro, Conxi; Brunet, Joan; Feliubadaló, Lidia; Iglesias, Silvia; Menéndez, Mireia; Teulé, Alex; Ballinger, Mandy L; Thomas, David M; Campbell, Ainsley; Field, Mike; Harris, Marion; Kirk, Judy; Pachter, Nicholas; Poplawski, Nicola; Susman, Rachel; Tucker, Kathy; Wallis, Mathew; Williams, Rachel; Cops, Elisa; Goldgar, David; James, Paul A; Spurdle, Amanda B
Clinical implications of VUS reclassification in a single-centre series from application of ACMG/AMP classification rules specified for BRCA1/2
2024 Innella, Giovanni; Ferrari, Simona; Miccoli, Sara; Luppi, Elena; Fortuno, Cristina; Parsons, Michael T; Spurdle, Amanda B; Turchetti, Daniela
Effectiveness and Impact of Transcript Analysis in Clinical Genetics Daily Practice
2024 Innella, Giovanni; Coccia, Emanuele; Cristalli, Carlotta Pia; Zacchi, Eliana; Calabrese, Sara; Bacchi, Isabelle; Palombo, Flavia; Taormina, Sara; Evangelisti, Cecilia; Lanzoni, Giulia; Carelli, Valerio; Diquigiovanni, Chiara; Ferrari, Simona; Panza, Emanuele; Rossi, Cesare; Vaisfeld, Alessandro; Bonora, Elena; Turchetti, Daniela
Familial DMRT1-related non-obstructive azoospermia: a case report
2024 Severi, Giulia; Ambrosini, Enrico; Caramanna, Luca; Monti, Luigi; Magini, Pamela; Innella, Giovanni
Hereditary breast and ovarian cancer genetic testing in unselected patients: example of private supplementation of public healthcare service
2024 Fiorentino, Francesca; Innella, Giovanni; Balducci, Federica; Marullo, Laura; Lanzoni, Giulia; Miccoli, Sara; Cardarelli, Laura; Turchetti, Daniela; Tempesta, Sergio
Light and shade of multigene panel testing for hereditary cancer: Examples from the real world
2024 Innella, Giovanni; Ferrari, Simona; Miccoli, Sara; Turchetti, Daniela
Long read sequencing on its way to the routine diagnostics of genetic diseases
2024 Olivucci, Giulia; Iovino, Emanuela; Innella, Giovanni; Turchetti, Daniela; Pippucci, Tommaso; Magini, Pamela
Unrecognised actionability for breast cancer risk variants identified in a national-level review of Australian familial cancer centres
2024 Fortuno, Cristina; Cops, Elisa J; Davidson, Aimee L; Hadler, Johanna; Innella, Giovanni; Mckenzie, Maddison E; Parsons, Michael; Campbell, Ainsley M; Dubowsky, Andrew; Fargas, Verna; Field, Michael J; Mar Fan, Helen G; Nichols, Cassandra B; Poplawski, Nicola K; Warwick, Linda; Williams, Rachel; Beshay, Victoria; Edwards, Caitlin; Johns, Andrea; Mcphillips, Mary; Kumar, Vanessa Siva; Scott, Rodney; Williams, Mark; Scott, Hamish; James, Paul A; Spurdle, Amanda B
Cancer risks by sex and variant type in PTEN Hamartoma Tumor Syndrome
2023 Hendricks, Linda A J; Hoogerbrugge, Nicoline; Mensenkamp, Arjen R; Brunet, Joan; Lleuger-Pujol, Roser; Høberg-Vetti, Hildegunn; Haavind, Marianne Tveit; Innella, Giovanni; Turchetti, Daniela; Aretz, Stefan; Spier, Isabel; Tischkowitz, Marc; Jahn, Arne; Links, Thera P; Olderode-Berends, Maran J W; Blatnik, Ana; Leter, Edward M; Evans, D Gareth; Woodward, Emma R; Steinke-Lange, Verena; Anastasiadou, Violetta C; Colas, Chrystelle; Villy, Marie-Charlotte; Benusiglio, Patrick R; Gerasimenko, Anna; Barili, Valeria; Branchaud, Maud; Houdayer, Claude; Tesi, Bianca; Yazicioglu, M Omer; van der Post, Rachel S; Schuurs-Hoeijmakers, Janneke H M; van Hest, Liselotte P; Adank, Muriel A; Duijkers, Floor; Nielsen, Maartje; Verbeek, Katja C J; van Ierland, Yvette; Giltay, Jacques C; Vos, Janet R
Cascade testing in Italian Hereditary Breast Ovarian Cancer families: a missed opportunity for cancer prevention?
2023 Trevisan, Lucia; Godino, Lea; Battistuzzi, Linda; Innella, Giovanni; Luppi, Elena; Buzzatti, Giulia; Gismondi, Viviana; Blondeaux, Eva; Bonelli, Luigina Ada; Turchetti, Daniela; Varesco, Liliana
Characterization of BRCA Deficiency in Ovarian Cancer
2023 Barbero, Giovanna; Zuntini, Roberta; Magini, Pamela; Desiderio, Laura; Bonaguro, Michela; Perrone, Anna Myriam; Rubino, Daniela; Grippa, Mina; De Leo, Antonio; Ceccarelli, Claudio; Godino, Lea; Miccoli, Sara; Ferrari, Simona; Santini, Donatella; De Iaco, Pierandrea; Zamagni, Claudio; Innella, Giovanni; Turchetti, Daniela
Factors predicting BRCA1/2 pathogenic variants in patients with ovarian cancer: a systematic review with meta-analysis
2023 Innella, Giovanni; Godino, Lea; Erini, Giulia; De Leo, Antonio; Santini, Donatella; Perrone, Anna Myriam; De Iaco, Pierandrea; Zamagni, Claudio; Turchetti, Daniela
New clinical features in an adult patient with Skraban-Deardorff syndrome
2022 Innella, Giovanni; Scarano, Emanuela; Palumbo, Pietro; Carella, Massimo; Severi, Giulia
Clinical spectrum and follow-up in six individuals with Lamb–Shaffer syndrome (SOX5)
2021 Innella G.; Greco D.; Carli D.; Magini P.; Giorgio E.; Galesi O.; Ferrero G.B.; Romano C.; Brusco A.; Graziano C.
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.
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.
| Titolo | Autore(i) | Anno | Periodico | Editore | Tipo | File |
|---|---|---|---|---|---|---|
| Cancer prognosis and treatment results in patients with PTEN Hamartoma Tumour Syndrome (PHTS)-a European cohort study | Hendricks, Linda A J; Verbeek, Katja C J; Schuurs-Hoeijmakers, Janneke H M; De Putter, Robin; Bre...ms, Hilde; Van Daele, Sien H; Anastasiadou, Violetta C; Foretová, Lenka; Benusiglio, Patrick R; Gerasimenko, Anna; Colas, Chrystelle; Villy, Marie-Charlotte; Houdayer, Claude; Branchaud, Maud; Hüneburg, Robert; Aretz, Stefan; Jahn, Arne; Steinke-Lange, Verena; Innella, Giovanni; Turchetti, Daniela; Barili, Valeria; Genuardi, Maurizio; Panfili, Arianna; Baldassarri, Margherita; Irmejs, Arvīds; De Jong, Mirjam M; Links, Thera P; Leter, Edward M; Bosch, Daniëlle G M; Donze, Stephany H; Van Der Post, Rachel S; Mensenkamp, Arjen R; Westdorp, Harm; Høberg-Vetti, Hildegunn; Tveit Haavind, Marianne; Jørgensen, Kjersti; Mæhle, Lovise; Briskemyr, Siri; Garcia, Juliette Dupont; Blatnik, Ana; Balmaña, Judith; Torres, Maite; Brunet, Joan; Lleuger-Pujol, Roser; Tham, Emma; Tischkowitz, Marc; Evans, D Gareth; Hyder, Zerin; Hoogerbrugge, Nicoline; Vos, Janet R | 2025-01-01 | BJC REPORTS | - | 1.01 Articolo in rivista | - |
| Clinical genetic services in the Emilia-Romagna region, Italy: current activity and open issues: a mixed-method study | Godino, Lea; Ambrosini, Enrico; Barili, Valeria; Graziano, Claudio; Garavelli, Livia; Calabrese, ...Olga; Neri, Marcella; Sangiorgi, Luca; Bertonazzi, Benedetta; Innella, Giovanni; Turchetti, Daniela; Percesepe, Antonio | 2025-01-01 | JOURNAL OF COMMUNITY GENETICS | - | 1.01 Articolo in rivista | Clinical genetic services in the Emilia-Romagna region, Italy- current activity and open issues- a mixed-method study.pdf |
| The risk of a second primary cancer in PTEN Hamartoma Tumor Syndrome (PHTS) | Hendricks, Linda A J; Verbeek, Katja C J; Schuurs-Hoeijmakers, Janneke H M; De Jong, Mirjam M; Li...nks, Thera P; Brems, Hilde; Aerden, Mio; Brunet, Joan; Lleuger-Pujol, Roser; Hüneburg, Robert; Aretz, Stefan; Colas, Chrystelle; Villy, Marie-Charlotte; Woodward, Emma R; Evans, D Gareth; Bosch, Daniëlle G M; Donze, Stephany H; Foretová, Lenka; Blatnik, Ana; Leter, Edward M; Tischkowitz, Marc; Jahn, Arne; De Putter, Robin; Dupont, Juliette; Briskemyr, Siri; Steinke-Lange, Verena; Baldassarri, Margherita; Anastasiadou, Violetta C; Irmejs, Arvīds; Oliveira, Carla; Van Der Post, Rachel S; Mensenkamp, Arjen R; Tesi, Bianca; Mu, Ninni; Benusiglio, Patrick R; Gerasimenko, Anna; Innella, Giovanni; Turchetti, Daniela; Houdayer, Claude; Branchaud, Maud; Høberg-Vetti, Hildegunn; Haavind, Marianne Tveit; Balmaña, Judith; Torres, Maite; Genuardi, Maurizio; Panfili, Arianna; Jørgensen, Kjersti; Mæhle, Lovise; Hoogerbrugge, Nicoline; Vos, Janet R | 2025-01-01 | GENETICS IN MEDICINE | - | 1.01 Articolo in rivista | - |
| Atypical cancer risk profile in carriers of Italian founder BRCA1 variant p.His1673del: Implications for classification and clinical management | Innella, Giovanni; Fortuno, Cristina; Caleca, Laura; Feng, Bing-Jian; Carroll, Courtney; Parsons,... Michael T; Miccoli, Sara; Montagna, Marco; Calistri, Daniele; Cortesi, Laura; Pasini, Barbara; Manoukian, Siranoush; Giachino, Daniela; Matricardi, Laura; Foti, Maria Cristina; Zampiga, Valentina; Piombino, Claudia; Barbieri, Elena; Lutati, Francesca Vignolo; Azzolini, Jacopo; Danesi, Rita; Arcangeli, Valentina; Caputo, Sandrine M; Boutry-Kryza, Nadia; Goussot, Vincent; Hiraki, Susan; Richardson, Marcy; Ferrari, Simona; Radice, Paolo; Spurdle, Amanda B; Turchetti, Daniela | 2024-01-01 | CANCER MEDICINE | - | 1.01 Articolo in rivista | Cancer Medicine - 2024 - Innella - Atypical cancer risk profile in carriers of Italian founder BRCA1 variant p His1673del .pdf; CAM4-13-e70114-s001.png; CAM4-13-e70114-s002.docx |
| Cancer Risks Associated With TP53 Pathogenic Variants: Maximum Likelihood Analysis of Extended Pedigrees for Diagnosis of First Cancers Beyond the Li-Fraumeni Syndrome Spectrum | Fortuno, Cristina; Feng, Bing-Jian; Carroll, Courtney; Innella, Giovanni; Kohlmann, Wendy; Lázaro..., Conxi; Brunet, Joan; Feliubadaló, Lidia; Iglesias, Silvia; Menéndez, Mireia; Teulé, Alex; Ballinger, Mandy L; Thomas, David M; Campbell, Ainsley; Field, Mike; Harris, Marion; Kirk, Judy; Pachter, Nicholas; Poplawski, Nicola; Susman, Rachel; Tucker, Kathy; Wallis, Mathew; Williams, Rachel; Cops, Elisa; Goldgar, David; James, Paul A; Spurdle, Amanda B | 2024-01-01 | JCO PRECISION ONCOLOGY | - | 1.01 Articolo in rivista | - |
| Clinical implications of VUS reclassification in a single-centre series from application of ACMG/AMP classification rules specified for BRCA1/2 | Innella, Giovanni; Ferrari, Simona; Miccoli, Sara; Luppi, Elena; Fortuno, Cristina; Parsons, Mich...ael T; Spurdle, Amanda B; Turchetti, Daniela | 2024-01-01 | JOURNAL OF MEDICAL GENETICS | - | 1.01 Articolo in rivista | Innella_VOR_2024.pdf |
| Effectiveness and Impact of Transcript Analysis in Clinical Genetics Daily Practice | Innella, Giovanni; Coccia, Emanuele; Cristalli, Carlotta Pia; Zacchi, Eliana; Calabrese, Sara; Ba...cchi, Isabelle; Palombo, Flavia; Taormina, Sara; Evangelisti, Cecilia; Lanzoni, Giulia; Carelli, Valerio; Diquigiovanni, Chiara; Ferrari, Simona; Panza, Emanuele; Rossi, Cesare; Vaisfeld, Alessandro; Bonora, Elena; Turchetti, Daniela | 2024-01-01 | CLINICAL GENETICS | - | 1.01 Articolo in rivista | Clinical Genetics - 2024 - Innella - Effectiveness and Impact of Transcript Analysis in Clinical Genetics Daily Practice.pdf; cge14684-sup-0001-supinfo.zip |
| Familial DMRT1-related non-obstructive azoospermia: a case report | Severi, Giulia; Ambrosini, Enrico; Caramanna, Luca; Monti, Luigi; Magini, Pamela; Innella, Giovanni | 2024-01-01 | JOURNAL OF ASSISTED REPRODUCTION AND GENETICS | - | 1.01 Articolo in rivista | s10815-024-03250-2.pdf |
| Hereditary breast and ovarian cancer genetic testing in unselected patients: example of private supplementation of public healthcare service | Fiorentino, Francesca; Innella, Giovanni; Balducci, Federica; Marullo, Laura; Lanzoni, Giulia; Mi...ccoli, Sara; Cardarelli, Laura; Turchetti, Daniela; Tempesta, Sergio | 2024-01-01 | FAMILIAL CANCER | - | 1.01 Articolo in rivista | - |
| Light and shade of multigene panel testing for hereditary cancer: Examples from the real world | Innella, Giovanni; Ferrari, Simona; Miccoli, Sara; Turchetti, Daniela | 2024-01-01 | TUMORI | - | 1.01 Articolo in rivista | - |
| Long read sequencing on its way to the routine diagnostics of genetic diseases | Olivucci, Giulia; Iovino, Emanuela; Innella, Giovanni; Turchetti, Daniela; Pippucci, Tommaso; Mag...ini, Pamela | 2024-01-01 | FRONTIERS IN GENETICS | - | 1.01 Articolo in rivista | fgene-15-1374860.pdf |
| Unrecognised actionability for breast cancer risk variants identified in a national-level review of Australian familial cancer centres | Fortuno, Cristina; Cops, Elisa J; Davidson, Aimee L; Hadler, Johanna; Innella, Giovanni; Mckenzie..., Maddison E; Parsons, Michael; Campbell, Ainsley M; Dubowsky, Andrew; Fargas, Verna; Field, Michael J; Mar Fan, Helen G; Nichols, Cassandra B; Poplawski, Nicola K; Warwick, Linda; Williams, Rachel; Beshay, Victoria; Edwards, Caitlin; Johns, Andrea; Mcphillips, Mary; Kumar, Vanessa Siva; Scott, Rodney; Williams, Mark; Scott, Hamish; James, Paul A; Spurdle, Amanda B | 2024-01-01 | EUROPEAN JOURNAL OF HUMAN GENETICS | - | 1.01 Articolo in rivista | 41431_2024_1705_MOESM2_ESM.xlsx; 41431_2024_1705_MOESM1_ESM.pdf; s41431-024-01705-9.pdf |
| Cancer risks by sex and variant type in PTEN Hamartoma Tumor Syndrome | Hendricks, Linda A J; Hoogerbrugge, Nicoline; Mensenkamp, Arjen R; Brunet, Joan; Lleuger-Pujol, R...oser; Høberg-Vetti, Hildegunn; Haavind, Marianne Tveit; Innella, Giovanni; Turchetti, Daniela; Aretz, Stefan; Spier, Isabel; Tischkowitz, Marc; Jahn, Arne; Links, Thera P; Olderode-Berends, Maran J W; Blatnik, Ana; Leter, Edward M; Evans, D Gareth; Woodward, Emma R; Steinke-Lange, Verena; Anastasiadou, Violetta C; Colas, Chrystelle; Villy, Marie-Charlotte; Benusiglio, Patrick R; Gerasimenko, Anna; Barili, Valeria; Branchaud, Maud; Houdayer, Claude; Tesi, Bianca; Yazicioglu, M Omer; van der Post, Rachel S; Schuurs-Hoeijmakers, Janneke H M; van Hest, Liselotte P; Adank, Muriel A; Duijkers, Floor; Nielsen, Maartje; Verbeek, Katja C J; van Ierland, Yvette; Giltay, Jacques C; Vos, Janet R | 2023-01-01 | JOURNAL OF THE NATIONAL CANCER INSTITUTE | - | 1.01 Articolo in rivista | djac188.pdf; djac188_supplementary_data.pdf |
| Cascade testing in Italian Hereditary Breast Ovarian Cancer families: a missed opportunity for cancer prevention? | Trevisan, Lucia; Godino, Lea; Battistuzzi, Linda; Innella, Giovanni; Luppi, Elena; Buzzatti, Giul...ia; Gismondi, Viviana; Blondeaux, Eva; Bonelli, Luigina Ada; Turchetti, Daniela; Varesco, Liliana | 2023-01-01 | FAMILIAL CANCER | - | 1.01 Articolo in rivista | - |
| Characterization of BRCA Deficiency in Ovarian Cancer | Barbero, Giovanna; Zuntini, Roberta; Magini, Pamela; Desiderio, Laura; Bonaguro, Michela; Perrone..., Anna Myriam; Rubino, Daniela; Grippa, Mina; De Leo, Antonio; Ceccarelli, Claudio; Godino, Lea; Miccoli, Sara; Ferrari, Simona; Santini, Donatella; De Iaco, Pierandrea; Zamagni, Claudio; Innella, Giovanni; Turchetti, Daniela | 2023-01-01 | CANCERS | - | 1.01 Articolo in rivista | cancers-15-01530-v2.pdf; cancers-15-01530-s001 (1).zip |
| Factors predicting BRCA1/2 pathogenic variants in patients with ovarian cancer: a systematic review with meta-analysis | Innella, Giovanni; Godino, Lea; Erini, Giulia; De Leo, Antonio; Santini, Donatella; Perrone, Anna... Myriam; De Iaco, Pierandrea; Zamagni, Claudio; Turchetti, Daniela | 2023-01-01 | JOURNAL OF CLINICAL PATHOLOGY | - | 1.01 Articolo in rivista | - |
| New clinical features in an adult patient with Skraban-Deardorff syndrome | Innella, Giovanni; Scarano, Emanuela; Palumbo, Pietro; Carella, Massimo; Severi, Giulia | 2022-01-01 | AMERICAN JOURNAL OF MEDICAL GENETICS. PART A | - | 1.01 Articolo in rivista | - |
| Clinical spectrum and follow-up in six individuals with Lamb–Shaffer syndrome (SOX5) | Innella G.; Greco D.; Carli D.; Magini P.; Giorgio E.; Galesi O.; Ferrero G.B.; Romano C.; Brusco... A.; Graziano C. | 2021-01-01 | AMERICAN JOURNAL OF MEDICAL GENETICS. PART A | - | 1.01 Articolo in rivista | - |
| 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 | - |
| 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 |