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 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, GD; 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 Giuseppe Donato Mangano, Malak Fouani, Daniela D'Amico, Valentina Di Felice, Rosario Barone
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
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 Francesca; Rocchitelli Luciana; Messina Luca Maria; Nardello Rosaria; Mangano Giuseppe Donato; Vanadia Francesca; Mangano Salvatore; Brighina Filippo; Raieli Vincenzo
Muscle Histopathological Abnormalities in a Patient With a CCT5 Mutation Predicted to Affect the Apical Domain of the Chaperonin Subunit
2022-06-02 Scalia, Federica; Barone, Rosario; Rappa, Francesca; Marino Gammazza, Antonella; Lo Celso, Fabrizio; Lo Bosco, Giosuè; Barone, Giampaolo; Antona, Vincenzo; Vadalà, Maria; Vitale, Alessandra Maria; Donato Mangano, Giuseppe; Amato, Domenico; Sentiero, Giusy; Macaluso, Filippo; Myburgh, Kathryn H.; Conway de Macario, Everly; Macario, Alberto J. L.; Giuffrè, Mario; Cappello, Francesco
NUP85 as a Neurodevelopmental Gene: From Podocyte to Neuron
2023-11-27 Antonella Gambadauro, Giuseppe Donato Mangano , Karol Galletta, Francesca Granata, Antonella Riva, Laura Massella, Isabella Guzzo, Giovanni Farello , Giovanna Scorrano, Ludovica Di Francesco, Giulio Di Donato, Carolina Ianni, Armando Di Ludovico, Saverio La Bella, Pasquale Striano, Stephanie Efthymiou, Henry Houlden, Rosaria Nardello, Roberto Chimenz
Recurrent missense variant in the nuclear export signal of FMR1 associated with FXS-like phenotype including intellectual disability, ASD, facial abnormalities
2022-01-25 Giuseppe Donato Mangano; Antonina Fontana; Vincenzo Salpietro; Vincenzo Antona; Giuseppa Renata Mangano; Rosaria Nardello
| 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-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, GD; 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 | Giuseppe Donato ManganoMalak FouaniValentina Di FeliceRosario Barone + | 01 - Contributo in rivista::1.09 Review essay (rassegna critica) | Giuseppe Donato Mangano, Malak Fouani, Daniela D'Amico, Valentina Di Felice, Rosario Barone | |
| 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 | |
| 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 Francesca; Rocchitelli Luciana; Messina Luca Maria; Nardello Rosaria; Mangano Giuseppe Donato; Vanadia Francesca; Mangano Salvatore; Brighina Filippo; Raieli Vincenzo | |
| 2-giu-2022 | Muscle Histopathological Abnormalities in a Patient With a CCT5 Mutation Predicted to Affect the Apical Domain of the Chaperonin Subunit | Scalia, FedericaBarone, RosarioRappa, FrancescaMarino Gammazza, AntonellaLo Celso, FabrizioLo Bosco, GiosuèBarone, GiampaoloAntona, VincenzoVadalà, MariaVitale, Alessandra MariaDonato Mangano, GiuseppeAmato, DomenicoMacaluso, FilippoGiuffrè, MarioCappello, Francesco + | 01 - Contributo in rivista::1.01 Articolo in rivista | Scalia, Federica; Barone, Rosario; Rappa, Francesca; Marino Gammazza, Antonella; Lo Celso, Fabrizio; Lo Bosco, Giosuè; Barone, Giampaolo; Antona, Vincenzo; Vadalà, Maria; Vitale, Alessandra Maria; Donato Mangano, Giuseppe; Amato, Domenico; Sentiero, Giusy; Macaluso, Filippo; Myburgh, Kathryn H.; Conway de Macario, Everly; Macario, Alberto J. L.; Giuffrè, Mario; Cappello, Francesco | |
| 27-nov-2023 | NUP85 as a Neurodevelopmental Gene: From Podocyte to Neuron | Giuseppe Donato ManganoFrancesca GranataRosaria Nardello + | 01 - Contributo in rivista::1.09 Review essay (rassegna critica) | Antonella Gambadauro, Giuseppe Donato Mangano , Karol Galletta, Francesca Granata, Antonella Riva, Laura Massella, Isabella Guzzo, Giovanni Farello , Giovanna Scorrano, Ludovica Di Francesco, Giulio Di Donato, Carolina Ianni, Armando Di Ludovico, Saverio La Bella, Pasquale Striano, Stephanie Efthymiou, Henry Houlden, Rosaria Nardello, Roberto Chimenz | |
| 25-gen-2022 | Recurrent missense variant in the nuclear export signal of FMR1 associated with FXS-like phenotype including intellectual disability, ASD, facial abnormalities | Giuseppe Donato ManganoAntonina FontanaGiuseppa Renata ManganoRosaria Nardello + | 01 - Contributo in rivista::1.01 Articolo in rivista | Giuseppe Donato Mangano; Antonina Fontana; Vincenzo Salpietro; Vincenzo Antona; Giuseppa Renata Mangano; Rosaria Nardello |