MANGANO, Giuseppe Donato
MANGANO, Giuseppe Donato
Biomedicina, Neuroscienze e Diagnostica avanzata
A BRIEF GUIDE TO THE ANATOMICAL DISSECTION OF THE STOMACH
2021-01-01 Tomasello,G; Mazzola,M; Gagliardo,CM; Scaglione,S; Zannelli,C; Bellante,G; Fucarino,A; Pitruzzella,A; Rà,W; Mangano,GD; Giambalvo,F; Saguto,D; Marino Gammazza,A; Carini,F
A complex epileptic and dysmorphic phenotype associated with a novel frameshift KDM5B variant and deletion of SCN gene cluster
2022-04-01 Mangano GD; Antona V; Calì E; Fontana A; Salpietro V; Houlden H; Veggiotti P; Nardello R
A novel de novo AP2M1 variant in a patient with attention-deficit/hyperactivity disorder, oppositional defiant disorder, and unexpected hemiplegic migraine
2025-01-01 Mangano, G.D.; Antona, V.; Santangelo, G.; Di Pasquale, G.; Colella, J.; Salpietro, V.; Mangano, G.R.; Raieli, V.
A novel mutation in KCNQ3-related benign familial neonatal epilepsy: electroclinical features and neurodevelopmental outcome
2019-01-01 Piro, Ettore; Nardello, Rosaria; Gennaro, Elena; Fontana, Antonina; Taglialatela, Maurizio; Mangano, Giuseppe Donato; Corsello, Giovanni; Mangano, Salvatore
A novel mutation of WDR62 gene associated with severe phenotype including infantile spasm, microcephaly, and intellectual disability.
2018-01-01 Nardello R, Fontana A, Antona V, Beninati A, Mangano GD, Stallone MC, Mangano S
A paradigmatic autistic phenotype associated with loss of PCDH11Y and NLGN4Y genes
2021-01-01 Nardello, R.; Antona, V.; Mangano, G.D.; Salpietro, V.; Mangano, S.; Fontana, A.
Age-dependent Epileptic Encephalopathy Associated With an Unusual Co-Occurrence of ZEB2 and SCN1A Variants
2020-01-01 Nardello, R.; Fontana, A.; Mangano, G.; Efthymiou, S.; Salpietro, V.; Houlden, H.; Mangano, S.
Benign familial infantile epilepsy associated with KCNQ3 mutation: a rare occurrence or an underestimated event?
2020-01-01 Nardello R, Mangano GD, Miceli F, Fontana A, Piro E, Salpietro V.
Broad neurodevelopmental features and cortical anomalies associated with a novel de novo KMT2A variant in Wiedemann-Steiner syndrome.
2021-02-01 Nardello R, Mangano GD, Fontana A, Gagliardo C, Midiri F, Borgia P, Brighina F, Raieli V, Mangano S, Salpietro V.
Cancer-related cachexia: insight for a multimodal approach
2023-06-26
Cancer‐Related Cachexia: The Vicious Circle between Inflammatory Cytokines, Skeletal Muscle, Lipid Metabolism and the Possible Role of Physical Training
2022-03-10 Mangano, G.D.; Fouani, M.; D'Amico, D.; Di Felice, V.; Barone, R.
Commonalities and distinctions between two neurodevelopmental disorder subtypes associated with SCN2A and SCN8A variants and literature review
2022-01-01 Mangano G.D.; Fontana A.; Antona V.; Salpietro V.; Mangano G.R.; Giuffre M.; Nardello R.
De novo GRIN2A variants associated with epilepsy and autism and literature review
2022-02-23 Mangano G.D.; Riva A.; Fontana A.; Salpietro V.; Mangano G.R.; Nobile G.; Orsini A.; Iacomino M.; Battini R.; Astrea G.; Striano P.; Nardello R.
Electroclinical features and outcome of ANKRD11-related KBG syndrome: A novel report and literature review
2021-02-01 Nardello R; Mangano GD; Antona V; Fontana A; Striano P; Giorgio E; Brusco A; Mangano S; Salpietro V
Exploring the Role of Heat Shock Proteins in Neuroimmune Modulation in Rheumatoid Arthritis: Insights from a Rat Model
2025-10-07 Fouani, M.; Scalia, F.; Mangano, G.D.; Rappa, F.; Abou-Kheir, W.; Leone, A.; Lawand, N.; Barone, R.
Familial hemiplegic migraine in pediatric patients: A genetic, clinical, and follow-up study
2023-08-01 Mangano, G.D.; Rita Capizzi, M.; Mantuano, E.; Veneziano, L.; Santangelo, G.; Quatrosi, G.; Nardello, R.; Raieli, V.
Further characterization of the BRSK2-associated neurodevelopmental disorder
2026-01-01 Singhal, P.; Hsieh, T.-.; Ehmke, N.; Bacchelli, E.; Viggiano, M.; Maestrini, E.; Visconti, P.; Posar, A.; Scaduto, M.C.; Vaisfeld, A.; Ronspies, C.; Burke, S.; Salgado, J.R.; Sa, J.; Ribeiro, S.; Shillington, A.; Aggarwal, A.; Dailey, C.; Saunders, C.; Del Viso, F.; Murali, C.N.; Macpherson, M.; Caluseriu, O.; Verloes, A.; Levy, J.; Capri, Y.; Kemmer, H.S.; Holtgrewe, M.; Boone, P.M.; Rodan, L.; Vasileiou, G.; Pauly, M.; Reis, A.; Herman, I.; Johnson, I.; Goel, H.; Rodriguez Barreto, A.M.; Faletra, F.; Mio, C.; Essawi, M.L.; Hassan, H.A.; Sharaf-Eldin, W.E.; Kishk, N.; Mangano, G.D.; Mangano, R.; Shields, A.K.; Ranells, J.D.; Hammer, T.B.; Velmans, C.; Netzer, C.; Winnerling, N.; Kolokotronis, K.; Seidl, B.; Rauch, A.; Fernandez-Jaen, A.; Rad, A.; Oprea, G.; Cullufi, P.; Tomori, S.; Beneteau, C.; Legendre, M.; Rooryck, C.; Klinkhammer, H.; Haack, T.B.; Khan, A.; Kick, J.; Bartholdi, D.; Braun, D.; Baldwin, E.E.; Viskochil, D.H.; Botto, L.D.; Lagroon, A.; Black, E.; Butler, K.M.; Ranza, E.; Macherel, M.; Desportes, V.; Pujalte, M.; Januel, L.; Keren, B.; Mignot, C.; Harion, M.; Voors, M.L.E.; Ockeloen, C.W.; Porta-Pelayo, J.; Popp, B.; Krawitz, P.; Sticht, H.; Gregor, A.; Zweier, C.
Heat Shock Proteins Alterations in Rheumatoid Arthritis
2022-03-03 Fouani M.; Basset C.; Mangano G.D.; Leone L.G.; Lawand N.B.; Leone A.; Barone R.
KCNT2-related disorders: phenotypes, functional and pharmacological properties
2023-04-16 Cioclu, Maria Cristina; Mosca, Ilaria; Ambrosino, Paolo; Puzo, Deborah; Bayat, Allan; Wortmann, Saskia B; Koch, Johannes; Strehlow, Vincent; Shirai, Kentaro; Matsumoto, Naomichi; Sanders, Stephan J; Michaud, Vincent; Legendre, Marine; Riva, Antonella; Striano, Pasquale; Muhle, Hiltrud; Pendziwiat, Manuela; Lesca, Gaetan; Mangano, Giuseppe Donato; Nardello, Rosaria; Lemke, Johannes R; Møller, Rikke S; Soldovieri, Maria Virginia; Rubboli, Guido; Taglialatela, Maurizio
Migraine in children under 6 years of age: A long-term follow-up study
2020-07-01 Marchese, F.; Rocchitelli, L.; Messina, L.M.; Nardello, R.; Mangano, G.D.; Vanadia, F.; Mangano, S.; Brighina, F.; Raieli, V.
| Data di pubblicazione | Titolo | Autori | Tipologia | Autore(i) | File |
|---|---|---|---|---|---|
| 1-gen-2021 | A BRIEF GUIDE TO THE ANATOMICAL DISSECTION OF THE STOMACH | Tomasello,GGagliardo,CMFucarino,APitruzzella,AMangano,GDGiambalvo,FSaguto,DMarino Gammazza,ACarini,F + | 01 - Contributo in rivista::1.01 Articolo in rivista | Tomasello,G; Mazzola,M; Gagliardo,CM; Scaglione,S; Zannelli,C; Bellante,G; Fucarino,A; Pitruzzella,A; Rà,W; Mangano,GD; Giambalvo,F; Saguto,D; Marino Gammazza,A; Carini,F | |
| 1-apr-2022 | A complex epileptic and dysmorphic phenotype associated with a novel frameshift KDM5B variant and deletion of SCN gene cluster | Mangano GDAntona VFontana ANardello R + | 01 - Contributo in rivista::1.01 Articolo in rivista | Mangano GD; Antona V; Calì E; Fontana A; Salpietro V; Houlden H; Veggiotti P; Nardello R | |
| 1-gen-2025 | A novel de novo AP2M1 variant in a patient with attention-deficit/hyperactivity disorder, oppositional defiant disorder, and unexpected hemiplegic migraine | Mangano G. D.Antona V.Mangano G. R. + | 01 - Contributo in rivista::1.01 Articolo in rivista | Mangano, G.D.; Antona, V.; Santangelo, G.; Di Pasquale, G.; Colella, J.; Salpietro, V.; Mangano, G.R.; Raieli, V. | |
| 1-gen-2019 | A novel mutation in KCNQ3-related benign familial neonatal epilepsy: electroclinical features and neurodevelopmental outcome | Piro, EttoreNardello, RosariaFontana, AntoninaMangano, Giuseppe DonatoCorsello, GiovanniMangano, Salvatore + | 01 - Contributo in rivista::1.01 Articolo in rivista | Piro, Ettore; Nardello, Rosaria; Gennaro, Elena; Fontana, Antonina; Taglialatela, Maurizio; Mangano, Giuseppe Donato; Corsello, Giovanni; Mangano, Salvatore | |
| 1-gen-2018 | A novel mutation of WDR62 gene associated with severe phenotype including infantile spasm, microcephaly, and intellectual disability. | Nardello RFontana AAntona VBeninati AMangano GDMangano S + | 01 - Contributo in rivista::1.01 Articolo in rivista | Nardello R, Fontana A, Antona V, Beninati A, Mangano GD, Stallone MC, Mangano S | |
| 1-gen-2021 | A paradigmatic autistic phenotype associated with loss of PCDH11Y and NLGN4Y genes | Nardello R.Antona V.Mangano G. D.Mangano S.Fontana A. + | 01 - Contributo in rivista::1.01 Articolo in rivista | Nardello, R.; Antona, V.; Mangano, G.D.; Salpietro, V.; Mangano, S.; Fontana, A. | |
| 1-gen-2020 | Age-dependent Epileptic Encephalopathy Associated With an Unusual Co-Occurrence of ZEB2 and SCN1A Variants | Nardello, RFontana, AMangano, GDMangano, S + | 01 - Contributo in rivista::1.01 Articolo in rivista | Nardello, R.; Fontana, A.; Mangano, G.; Efthymiou, S.; Salpietro, V.; Houlden, H.; Mangano, S. | |
| 1-gen-2020 | Benign familial infantile epilepsy associated with KCNQ3 mutation: a rare occurrence or an underestimated event? | Nardello RMangano GDFontana APiro E + | 01 - Contributo in rivista::1.01 Articolo in rivista | Nardello R, Mangano GD, Miceli F, Fontana A, Piro E, Salpietro V. | |
| 1-feb-2021 | Broad neurodevelopmental features and cortical anomalies associated with a novel de novo KMT2A variant in Wiedemann-Steiner syndrome. | Nardello RMangano GDFontana AGagliardo CMidiri FBrighina FMangano S + | 01 - Contributo in rivista::1.01 Articolo in rivista | Nardello R, Mangano GD, Fontana A, Gagliardo C, Midiri F, Borgia P, Brighina F, Raieli V, Mangano S, Salpietro V. | |
| 26-giu-2023 | Cancer-related cachexia: insight for a multimodal approach | MANGANO, Giuseppe Donato | 04 - Tesi di dottorato::4.2 Tesi di dottorato | - | |
| 10-mar-2022 | Cancer‐Related Cachexia: The Vicious Circle between Inflammatory Cytokines, Skeletal Muscle, Lipid Metabolism and the Possible Role of Physical Training | Mangano G. D.Fouani M.D'amico D.Di Felice V.Barone R. | 01 - Contributo in rivista::1.09 Review essay (rassegna critica) | Mangano, G.D.; Fouani, M.; D'Amico, D.; Di Felice, V.; Barone, R. | |
| 1-gen-2022 | Commonalities and distinctions between two neurodevelopmental disorder subtypes associated with SCN2A and SCN8A variants and literature review | Mangano G. D.Fontana A.Antona V.Mangano G. R.Giuffre M.Nardello R. + | 01 - Contributo in rivista::1.01 Articolo in rivista | Mangano G.D.; Fontana A.; Antona V.; Salpietro V.; Mangano G.R.; Giuffre M.; Nardello R. | |
| 23-feb-2022 | De novo GRIN2A variants associated with epilepsy and autism and literature review | Mangano G. D.Fontana A.Mangano G. R.Nobile G.Nardello R. + | 01 - Contributo in rivista::1.01 Articolo in rivista | Mangano G.D.; Riva A.; Fontana A.; Salpietro V.; Mangano G.R.; Nobile G.; Orsini A.; Iacomino M.; Battini R.; Astrea G.; Striano P.; Nardello R. | |
| 1-feb-2021 | Electroclinical features and outcome of ANKRD11-related KBG syndrome: A novel report and literature review | Nardello RMangano GDAntona VFontana AMangano S + | 01 - Contributo in rivista::1.01 Articolo in rivista | Nardello R; Mangano GD; Antona V; Fontana A; Striano P; Giorgio E; Brusco A; Mangano S; Salpietro V | |
| 7-ott-2025 | Exploring the Role of Heat Shock Proteins in Neuroimmune Modulation in Rheumatoid Arthritis: Insights from a Rat Model | Mangano G. D.Rappa F.Leone A.Barone R. + | 01 - Contributo in rivista::1.01 Articolo in rivista | Fouani, M.; Scalia, F.; Mangano, G.D.; Rappa, F.; Abou-Kheir, W.; Leone, A.; Lawand, N.; Barone, R. | |
| 1-ago-2023 | Familial hemiplegic migraine in pediatric patients: A genetic, clinical, and follow-up study | Giuseppe Donato ManganoGiuseppe QuatrosiRosaria Nardello + | 01 - Contributo in rivista::1.01 Articolo in rivista | Mangano, G.D.; Rita Capizzi, M.; Mantuano, E.; Veneziano, L.; Santangelo, G.; Quatrosi, G.; Nardello, R.; Raieli, V. | |
| 1-gen-2026 | Further characterization of the BRSK2-associated neurodevelopmental disorder | Mangano G. D.Mangano R. + | 01 - Contributo in rivista::1.01 Articolo in rivista | Singhal, P.; Hsieh, T.-.; Ehmke, N.; Bacchelli, E.; Viggiano, M.; Maestrini, E.; Visconti, P.; Posar, A.; Scaduto, M.C.; Vaisfeld, A.; Ronspies, C.; Burke, S.; Salgado, J.R.; Sa, J.; Ribeiro, S.; Shillington, A.; Aggarwal, A.; Dailey, C.; Saunders, C.; Del Viso, F.; Murali, C.N.; Macpherson, M.; Caluseriu, O.; Verloes, A.; Levy, J.; Capri, Y.; Kemmer, H.S.; Holtgrewe, M.; Boone, P.M.; Rodan, L.; Vasileiou, G.; Pauly, M.; Reis, A.; Herman, I.; Johnson, I.; Goel, H.; Rodriguez Barreto, A.M.; Faletra, F.; Mio, C.; Essawi, M.L.; Hassan, H.A.; Sharaf-Eldin, W.E.; Kishk, N.; Mangano, G.D.; Mangano, R.; Shields, A.K.; Ranells, J.D.; Hammer, T.B.; Velmans, C.; Netzer, C.; Winnerling, N.; Kolokotronis, K.; Seidl, B.; Rauch, A.; Fernandez-Jaen, A.; Rad, A.; Oprea, G.; Cullufi, P.; Tomori, S.; Beneteau, C.; Legendre, M.; Rooryck, C.; Klinkhammer, H.; Haack, T.B.; Khan, A.; Kick, J.; Bartholdi, D.; Braun, D.; Baldwin, E.E.; Viskochil, D.H.; Botto, L.D.; Lagroon, A.; Black, E.; Butler, K.M.; Ranza, E.; Macherel, M.; Desportes, V.; Pujalte, M.; Januel, L.; Keren, B.; Mignot, C.; Harion, M.; Voors, M.L.E.; Ockeloen, C.W.; Porta-Pelayo, J.; Popp, B.; Krawitz, P.; Sticht, H.; Gregor, A.; Zweier, C. | |
| 3-mar-2022 | Heat Shock Proteins Alterations in Rheumatoid Arthritis | Fouani M.Basset C.Mangano G. D.Leone A.Barone R. + | 01 - Contributo in rivista::1.09 Review essay (rassegna critica) | Fouani M.; Basset C.; Mangano G.D.; Leone L.G.; Lawand N.B.; Leone A.; Barone R. | |
| 16-apr-2023 | KCNT2-related disorders: phenotypes, functional and pharmacological properties | Mangano, Giuseppe DonatoNardello, RosariaTaglialatela, Maurizio + | 01 - Contributo in rivista::1.01 Articolo in rivista | Cioclu, Maria Cristina; Mosca, Ilaria; Ambrosino, Paolo; Puzo, Deborah; Bayat, Allan; Wortmann, Saskia B; Koch, Johannes; Strehlow, Vincent; Shirai, Kentaro; Matsumoto, Naomichi; Sanders, Stephan J; Michaud, Vincent; Legendre, Marine; Riva, Antonella; Striano, Pasquale; Muhle, Hiltrud; Pendziwiat, Manuela; Lesca, Gaetan; Mangano, Giuseppe Donato; Nardello, Rosaria; Lemke, Johannes R; Møller, Rikke S; Soldovieri, Maria Virginia; Rubboli, Guido; Taglialatela, Maurizio | |
| 1-lug-2020 | Migraine in children under 6 years of age: A long-term follow-up study | Messina Luca MariaNardello RosariaMangano Giuseppe DonatoMangano SalvatoreBrighina Filippo + | 01 - Contributo in rivista::1.01 Articolo in rivista | Marchese, F.; Rocchitelli, L.; Messina, L.M.; Nardello, R.; Mangano, G.D.; Vanadia, F.; Mangano, S.; Brighina, F.; Raieli, V. |