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.
2020-01-01 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
2020-01-01 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.
Migraine in children under 6 years of age: A long-term follow-up study
2020-01-01 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
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
The largest caucasian kindred with dentatorubral-pallidoluysian atrophy: A founder mutation in italy
2019-01-01 Grimaldi S; Cupidi C; Smirne N; Bernardi L; Giacalone F; Piccione G; Basiricò S; Mangano GD; Nardello R; Orsi L; Grosso E; Laganà V; Mitolo M; Maletta RG; Bruni AC
Two distinct phenotypes, hemiplegic migraine and episodic Ataxia type 2, caused by a novel common CACNA1A variant
2020-01-01 Nardello, Rosaria; Plicato, Giorgia; Mangano, Giuseppe Donato; Gennaro, Elena; Mangano, Salvatore; Brighina, Filippo; Raieli, Vincenzo; Fontana, Antonina
| 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-gen-2020 | 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-gen-2020 | 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. | |
| 1-gen-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 | |
| 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 | |
| 1-gen-2019 | The largest caucasian kindred with dentatorubral-pallidoluysian atrophy: A founder mutation in italy | Mangano GDNardello R + | 01 - Contributo in rivista::1.01 Articolo in rivista | Grimaldi S; Cupidi C; Smirne N; Bernardi L; Giacalone F; Piccione G; Basiricò S; Mangano GD; Nardello R; Orsi L; Grosso E; Laganà V; Mitolo M; Maletta RG; Bruni AC | |
| 1-gen-2020 | Two distinct phenotypes, hemiplegic migraine and episodic Ataxia type 2, caused by a novel common CACNA1A variant | Nardello, RosariaPlicato, GiorgiaMangano, Giuseppe DonatoMangano, SalvatoreBrighina, FilippoFontana, Antonina + | 01 - Contributo in rivista::1.01 Articolo in rivista | Nardello, Rosaria; Plicato, Giorgia; Mangano, Giuseppe Donato; Gennaro, Elena; Mangano, Salvatore; Brighina, Filippo; Raieli, Vincenzo; Fontana, Antonina |