Sfoglia per AUTORE
GIORDANO M
Collezione AOU Novara

  

Items : 24

2025
AOU Novara

Luppino G; Wasniewska M; Giordano M; Pepe G; Morabito LA; Porri D; Aversa T; Corica D;

Towards a genetic obesity risk score in a single-center study of children and adolescents with obesity. in Scientific reports / Sci Rep. 2025 Apr 23;15(1):14180. doi: 10.1038/s41598-025-96883-x.
2025
AOU Novara

Giordano M; Mellone S; Bellone S; Prodam F; Petri A; Andorno S; Partenope C; Monteleone G; Rabbone I;

The Changing Landscape of Neonatal Diabetes Mellitus in Italy Between 2003 and 2022. in The Journal of clinical endocrinology and metabolism / J Clin Endocrinol Metab. 2024 Aug 13;109(9):2349-2357. doi: 10.1210/clinem/dgae095.
2024
AOU Novara

Rapini N; Delvecchio M; Mucciolo M; Ruta R; Rabbone I; Cherubini V; Zucchini S; Cianfarani S; Prandi E; Schiaffini R; Bizzarri C; Piccini B; Maltoni G; Predieri B; Minuto N; Di Paola R; Giordano M; Tinto N; Grasso V; Russo L; Tiberi V; Scaramuzza A; Frontino G; Maggio MC; Musolino G; Piccinno E; Tinti D; Carrera P; Mozzillo E; et alii...

Role of CES1 and ABCB1 Genetic Polymorphisms on Functional Response to Dabigatran in Patients with Atrial Fibrillation. in Journal of clinical medicine / J Clin Med. 2024 Apr 26;13(9):2545. doi: 10.3390/jcm13092545.
2024
AOU Novara

Cumitini L; Renda G; Giordano M; Rolla R; Shail T; Sacchetti S; Iezzi L; Giacomini L; Zanotti V; Auciello R; Angilletta I; Foglietta M; Zucchelli M; Antonucci I; Stuppia L; Gallina S; Dianzani U; Patti G;

Endocrine features of Prader-Willi syndrome: a narrative review focusing on genotype-phenotype correlation. in Frontiers in endocrinology / Front Endocrinol (Lausanne). 2024 Apr 26;15:1382583. doi: 10.3389/fendo.2024.1382583. eCollection 20
2024
AOU Novara

Madeo SF; Zagaroli L; Vandelli S; Calcaterra V; Crinò A; De Sanctis L; Faienza MF; Fintini D; Guazzarotti L; Licenziati MR; Mozzillo E; Pajno R; Scarano E; Street ME; Wasniewska M; Bocchini S; Bucolo C; Buganza R; Chiarito M; Corica D; Di Candia F; Francavilla R; Fratangeli N; Improda N; Morabito LA; Mozzato C; Rossi V; Schiavariello C; Farello G; et alii...

Temporal correlation between the first melanoma and the first noncutaneous tumor in CKDN2A genotyped patients. in Melanoma research / Melanoma Res. 2023 Oct 1;33(5):425-430. doi: 10.1097/CMR.0000000000000906. Epub 2023 Jun 21.
2023
AOU Novara

Gironi LC; Esposto E; Zottarelli F; Giorgione R; Farinelli P; Zavattaro E; Cammarata E; Di Cristo N; Ogliara P; Camillo L; Giordano M; Mellone S; Pasini B; Ambrosi A; Savoia P;

The risks associated with percutaneous native kidney biopsies: a prospective study. in Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association / Nephrol Dial Transplant. 2023 Feb 28;38(3):655-663. doi: 10.1093/ndt/gfac177.
2023
AO Cuneo
AOU Novara

Sottini L; Gintoli E; Brugnano R; Zanchelli F; Abaterusso C; Vernaglione L; Garozzo M; Penna D; De Giovanni P; Mattozzi F; Distefano G; Piemontese M; Micarelli D; Baraldi O; Bruno F; Spatola L; Bonomini M; Di Luca M; Seminara G; Giannese D; Giordano M; Cianci R; Ferrantelli A; Infante B; Manenti L; Santoro D; Moggia E; Granata A; Aucella F; et alii...

2023
ASL Città di Torino
AOU Città della Salute di Torino
AOU Novara

Bria E; Cognetti F; Crinò L; De Laurentiis M; Del Mastro L; De Placido S; Beano A; Zambelli A; Mustacchi G; Turletti A; Verusio C; Tonini G; Tinari N; Spazzapan S; Tagliaferri P; Romagnoli E; Sarobba G; Mattioli R; Michelotti A; Montemurro F; Putzu C; Riccardi F; Ricciardi G; Marchetti P; Livi L; Giotta F; Giovanardi F; Latini L; Gennari A; et alii...

Case report: Better late than never, but sooner is better: switch from CSII to sulfonylureas in two patients with neonatal diabetes due to KCNJ11 variants. in Frontiers in endocrinology / Front Endocrinol (Lausanne). 2023 May 11;14:1143736. doi: 10.3389/fendo.2023.1143736. eCollection 20
2023
AOU Novara

Mancioppi V; Pozzi E; Zanetta S; Missineo A; Savastio S; Barbetti F; Mellone S; Giordano M; Rabbone I;

A new mutation in the CAVIN1/PTRF gene in two siblings with congenital generalized lipodystrophy type 4: case reports and review of the literature. in Frontiers in endocrinology / Front Endocrinol (Lausanne). 2023 Jul 12;14:1212729. doi: 10.3389/fendo.2023.1212729. eCollection 20
2023
AOU Novara

Mancioppi V; Daffara T; Romanisio M; Ceccarini G; Pelosini C; Santini F; Bellone S; Mellone S; Baricich A; Rabbone I; Aimaretti G; Akinci B; Giordano M; Prodam F;

Copy number variations residing outside the SHOX enhancer region are involved in Short Stature and Léri-Weill dyschondrosteosis. in Molecular genetics & genomic medicine / Mol Genet Genomic Med. 2022 Jan;10(1):e1793. doi: 10.1002/mgg3.1793. Epub 2021 Nov 23.
2022
AOU Alessandria
AOU Città della Salute di Torino
AOU Novara

Giordano M; Bellone S; Prodam F; Follenzi A; Al Essa W; Secco A; Monzani A; Babu D; Mellone S; Cucci A; Vannelli S; Fanelli A;

Determinants of long COVID among adults hospitalized for SARS-CoV-2 infection: A prospective cohort study. in Frontiers in immunology / Front Immunol. 2022 Dec 19;13:1038227. doi: 10.3389/fimmu.2022.1038227. eCollection 2022.
2022
AOU Novara

Bellan M; Apostolo D; Albè A; Crevola M; Errica N; Ratano G; Tonello S; Minisini R; D'Onghia D; Baricich A; Patrucco F; Zeppegno P; Gramaglia C; Balbo PE; Cappellano G; Casella S; Chiocchetti A; Clivati E; Giordano M; Manfredi M; Patti G; Pinato DJ; Puricelli C; Raineri D; Rolla R; Sainaghi PP; Pirisi M;

2021
AOU Novara

Mellone S; Zavattaro M; Vurchio D; Ronzani S; Caputo M; Leone I; Prodam F; Giordano M;

Long-term sequelae are highly prevalent one year after hospitalization for severe COVID-19. in Scientific reports / Sci Rep. 2021 Nov 22;11(1):22666. doi: 10.1038/s41598-021-01215-4.
2021
AOU Novara

Bellan M; Baricich A; Patrucco F; Zeppegno P; Gramaglia C; Balbo PE; Carriero A; Amico CS; Avanzi GC; Barini M; Battaglia M; Bor S; Cantaluppi V; Cappellano G; Ceruti F; Chiocchetti A; Clivati E; Giordano M; Cuneo D; Gambaro E; Gattoni E; Loro A; Manfredi M; Morosini U; Murano F; Paracchini E; Patti G; Pinato DJ; Raineri D; et alii...

Consumption of complement in a 26-year-old woman with severe thrombotic thrombocytopenia after ChAdOx1 nCov-19 vaccination. in Journal of autoimmunity / J Autoimmun. 2021 Nov;124:102728. doi: 10.1016/j.jaut.2021.102728. Epub 2021 Sep 27.
2021
AOU Novara

Cugno M; Macor P; Giordano M; Manfredi M; Griffini S; Grovetti E; De Maso L; Mellone S; Valenti L; Prati D; Bonato S; Comi G; Artoni A; Meroni PL; Peyvandi F;

Variants in the 5'UTR reduce SHOX expression and contribute to SHOX haploinsufficiency. in European journal of human genetics : EJHG / Eur J Hum Genet. 2021 Jan;29(1):110-121. doi: 10.1038/s41431-020-0676-y. Epub 2020 Jul 9.
2021
AOU Città della Salute di Torino
AOU Novara

Prodam F; De Sanctis L; Stuppia L; Monzani A; Vinci G; Bellone S; Grandone A; Corrado L; Essa WA; Baffico AM; Mellone S; Fanelli A; Vannelli S; Babu D; Giordano M;

Metabolomics Diagnosis of COVID-19 from Exhaled Breath Condensate. in Metabolites / Metabolites. 2021 Dec 6;11(12):847. doi: 10.3390/metabo11120847.
2021
AOU Alessandria
AOU Novara

Rolla R; Chiocchetti A; Giordano M; Brustia D; Patti G; Balbo PE; Bellan M; Sainaghi PP; Castello L; Khoso S; Amede E; Barberis E; Romani G; Manfredi M; Vaschetto R;

Retrospective Diagnosis of a Novel ACAN Pathogenic Variant in a Family With Short Stature: A Case Report and Review of the Literature. in Frontiers in genetics / Front Genet. 2021 Aug 12;12:708864. doi: 10.3389/fgene.2021.708864. eCollection 2021.
2021
AOU Novara

Mancioppi V; Prodam F; Mellone S; Ricotti R; Giglione E; Grasso N; Vurchio D; Petri A; Rabbone I; Giordano M; Bellone S;

The first case of the TARDBP p.G294V mutation in a homozygous state: is a single pathogenic allele sufficient to cause ALS? in Amyotrophic lateral sclerosis & frontotemporal degeneration / Amyotroph Lateral Scler Frontotemporal Degener. 2020 May;21(3-4):273-279. doi: 10.1080/21678421.2019
2020
AOU Novara

Corrado L; Pensato V; Croce R; Di Pierro A; Mellone S; Dalla Bella E; Salsano E; Paraboschi EM; Giordano M; Saraceno M; Mazzini L; Gellera C; D'Alfonso S;

Hereditary Deficiency of the Second Component of Complement: Early Diagnosis and 21-Year Follow-Up of a Family. in Medicina (Kaunas, Lithuania) / Medicina (Kaunas). 2020 Mar 10;56(3):120. doi: 10.3390/medicina56030120.
2020
AOU Novara

Dellepiane RM; Baselli LA; Cazzaniga M; Lougaris V; Macor P; Giordano M; Gualtierotti R; Cugno M;

Genetic Analyses in Dent Disease and Characterization of CLCN5 Mutations in Kidney Biopsies. in International journal of molecular sciences / Int J Mol Sci. 2020 Jan 14;21(2):516. doi: 10.3390/ijms21020516.
2020
AOU Novara

Gianesello L; Ceol M; Bertoldi L; Terrin L; Priante G; Murer L; Peruzzi L; Giordano M; Paglialonga F; Cantaluppi V; Musetti C; Valle G; Del Prete D; Anglani F; Network DDI;

Identification of Haptoglobin as a Readout of rhGH Therapy in GH Deficiency. in The Journal of clinical endocrinology and metabolism / J Clin Endocrinol Metab. 2019 Nov 1;104(11):5263-5273. doi: 10.1210/jc.2019-00562.
2019
AOU Novara

De Feudis M; Walker GE; Genoni G; Manfredi M; Agosti E; Giordano M; Caputo M; Di Trapani L; Marengo E; Aimaretti G; Filigheddu N; Bellone S; Bona G; Prodam F;

Ovotesticular Disorder of Sex Development: A Rare Case of Lateral Subtype 45X/46XY kariotype Diagnosed in Adulthood. in Urology / Urology. 2019 Jul;129:68-70. doi: 10.1016/j.urology.2019.04.008. Epub 2019 Apr 18.
2019
AOU Novara

Caputo M; Mele C; Zavattaro M; Samà MT; Giordano M; Umari P; Volpe A; Aimaretti G; Prodam F;

Invasive meningococcal disease in three siblings with hereditary deficiency of the 8(th) component of complement: evidence for the importance of an early diagnosis. in Orphanet journal of rare diseases / Orphanet J Rare Dis. 2016 May 17;11(1):64. doi: 10.1186/s13023-016-0448-5.
2016
AOU Novara

Dellepiane RM; Dell'Era L; Pavesi P; Macor P; Giordano M; De Maso L; Pietrogrande MC; Cugno M;

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