Sfoglia per AUTORE
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Collezione AOU Novara

  

Items : 4

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...

The Silent Epidemic of Diabetic Ketoacidosis at Diagnosis of Type 1 Diabetes in Children and Adolescents in Italy During the COVID-19 Pandemic in 2020. in Frontiers in endocrinology / Front Endocrinol (Lausanne). 2022 Jun 17;13:878634. doi: 10.3389/fendo.2022.878634. eCollection 2022
2022
AOU Città della Salute di Torino
AOU Novara

Gesuita R; Rabbone I; Zucchini S; Moretti C; Pozzi E; Matteoli MC; Lenzi L; Iannilli A; Talarico V; Maltoni G; Musolino G; Franco F; Tornese G; Cauvin V; Franceschi R; Guerraggio LP; Trada M; Tinti D; De Sanctis L; Meloni G; Rutigliano I; Schiaffini R; Patera PI; Pampanini V; Lasagni A; Berioli MG; Calcaterra V; Iovane B; Cardella F; et alii...

Corrigendum: The silent epidemic of diabetic ketoacidosis at diagnosis of type 1 diabetes in children and adolescents in italy during the covid-19 pandemic in 2020. in Frontiers in endocrinology / Front Endocrinol (Lausanne). 2022 Aug 4;13:977211. doi: 10.3389/fendo.2022.977211. eCollection 2022.
2022
AOU Città della Salute di Torino
AOU Novara

Zucchini S; Rabbone I; Moretti C; Pozzi E; Matteoli MC; Lenzi L; Iannilli A; Talarico V; Maltoni G; Musolino G; Franco F; Tornese G; Cauvin V; Guerraggio LP; Franceschi R; Trada M; De Sanctis L; Tinti D; Meloni G; Schiaffini R; Rutigliano I; Patera PI; Pampanini V; Lasagni A; Berioli MG; Iovane B; Calcaterra V; Piredda G; Cardella F; et alii...

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;