Sfoglia per AUTORE
SANTINI F
Collezione AOU Novara
Items : 2
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
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;
Very-low-calorie ketogenic diet (VLCKD) in the management of metabolic diseases: systematic review and consensus statement from the Italian Society of Endocrinology (SIE). in Journal of endocrinological investigation / J Endocrinol Invest. 2019 Nov;42(11):1365-1386. doi: 10.1007/s40618-019-01061-2. Epub 2019 May 20.
2019
AOU Novara
AOU Novara
Caprio M; Infante M; Moriconi E; Armani A; Fabbri A; Mantovani G; Mariani S; Lubrano C; Poggiogalle E; Migliaccio S; Donini LM; Basciani S; Cignarelli A; Conte E; Ceccarini G; Bogazzi F; Cimino L; Condorelli RA; La Vignera S; Calogero AE; Gambineri A; Vignozzi L; Prodam F; Aimaretti G; Linsalata G; Buralli S; Monzani F; Aversa A; Vettor R; et alii...