MOIA, STEFANIA

MOIA, STEFANIA  

Dipartimento di Scienze della Salute  

Mostra records
Risultati 1 - 12 di 12 (tempo di esecuzione: 0.014 secondi).
Titolo Data di pubblicazione Autore(i) File
A novel HESX1 splice mutation causes isolated GH deficiency by interfering with mRNA processing 1-gen-2011 Vivenza, D; Godi, M; Faienza, Mf; Mellone, S; Moia, Stefania; Rapa, Anna; Petri, Antonella; Bellone, Simonetta; Riccomagno, S; Cavallo, L; Giordano, Mara; Bona, Gianni
Adiponectin oligomers are similarly distributed in adequate-for-gestational-age obese children irrespective of feeding in their first year 1-gen-2015 Prodam, Flavia; Roccio, Marta; Trovato, Letizia; Ricotti, Roberta; Moia, Stefania; Giglione, Enza; Petri, Antonella; Walker, Gillian Elisabeth; Bellone, Simonetta; Bona, Gianni
Compound heterozygosity for two GHR missense mutations in a patient affected by Laron Syndrome: A case report 1-gen-2017 Moia, Stefania; Tessaris, Daniele; Einaudi, Silvia; De Sanctis, Luisa; Bona, Gianni; Bellone, Simonetta; Prodam, Flavia
Endocrine disorders in childhood and adolescence. Natural history of subclinical hypothyroidism in children and adolescents and potential effects of replacement therapy: a review. 1-gen-2012 Monzani, A; Prodam, Flavia; Rapa, Anna; Moia, Stefania; Agarla, V; Bellone, Simonetta; Bona, Gianni
Interictal ghrelin levels in adult patients with epilepsy. 1-gen-2014 Varrasi, C; Strigaro, Gionata; Sola, M; Falletta, L; Moia, Stefania; Prodam, Flavia; Cantello, Roberto
Involvement of genes related to inflammation and cell cycle in Idiopathic Short Stature. 1-gen-2013 Trovato, L; Prodam, Flavia; Genoni, G; De Rienzo, F; Walker, Gillian Elisabeth; Moia, Stefania; Riccomagno, S; Bellone, Simonetta; Bona, Gianni
Isolated GHD: investigation and implication of JAK/STAT related genes before and after rhGH treatment. 1-gen-2012 Trovato, L; Riccomagno, S; Prodam, Flavia; Genoni, G; Walker, Gillian Elisabeth; Moia, Stefania; Bellone, Simonetta; Bona, Gianni
Obestatin levels are associated with C-peptide and anti-insulin antibodies at the onset whereas unacylated and acylated ghrelin levels are not predictive of long-term metabolic control in children with type 1 diabetes. 1-gen-2014 Prodam, Flavia; Cadario, F; Bellone, Simonetta; Trovato, L; Moia, Stefania; Pozzi, E; Savastio, S; Bona, Gianni
Pediatric obesity and vitamin D deficiency: a proteomic approach identifies multimeric adiponectin as a key link between these conditions. 1-gen-2014 Walker, Gillian Elisabeth; Ricotti, R; Roccio, Marta; Moia, Stefania; Bellone, Simonetta; Prodam, Flavia; Bona, Gianni
The W520X mutation in the TSHR gene brings on subclinical hypothyroidism through an haploinsufficiency mechanism. 1-gen-2013 Moia, Stefania; Godi, M; Walker, Gillian Elisabeth; Roccio, M; Agretti, P; Tonacchera, M; Berardi, R; Bellone, Simonetta; Prodam, Flavia; Giordano, Mara; Bona, Gianni
Tourette syndrome in a patient with resistance to thyroid hormone syndrome. 1-gen-2013 Monzani, Alice; Bona, Gianni; Moia, Stefania; Corrias, A; Miglio, C; Cavanna, A. E.
Unacylated, acylated ghrelin and obestatin levels are differently inhibited by oral glucose load in pediatric obesity: Association with insulin sensitivity and metabolic alterations. 1-gen-2011 Prodam, Flavia; Trovato, L; Demarchi, I; Busti, A; Petri, Antonella; Moia, Stefania; Walker, Gillian Elisabeth; Aimaretti, Gianluca; Bona, Gianni; Bellone, Simonetta