Sfoglia per AUTORE
MELLONE S
Collezione AOU Novara

  

Items : 10

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;

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;

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;

2021
AOU Novara

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

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;

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;

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