V. Grasso

发表

Minimal incidence of neonatal/infancy onset diabetes in Italy is 1:90,000 live births

C. Nichols, R. Schiaffini, F. Meschi, 2011, Acta Diabetologica.

Monogenic Diabetes Accounts for 6.3% of Cases Referred to 15 Italian Pediatric Diabetes Centers During 2007 to 2012

G. d’Annunzio, G. Salzano, G. Maltoni, 2017, The Journal of clinical endocrinology and metabolism.

A possible role of transglutaminase 2 in the nucleus of INS-1E and of cells of human pancreatic islets

S. Petrini, F. Bertuzzi, M. Alessio, 2014, Journal of proteomics.

[Severe type A insulin resistance syndrome due to a mutation in the insulin receptor gene].

J. Argente, P. Ros, F. Barbetti, 2015, Anales de pediatria.

Six cases with severe insulin resistance (SIR) associated with mutations of insulin receptor: Is a Bartter-like syndrome a feature of congenital SIR?

F. Cerutti, E. Bonora, I. Rabbone, 2013, Acta Diabetologica.

Can HbA1c combined with fasting plasma glucose help to assess priority for GCK-MODY vs HNF1A-MODY genetic testing?

G. d’Annunzio, G. Salzano, A. Franzese, 2018, Acta Diabetologica.

Low Prevalence of HNF1A Mutations After Molecular Screening of Multiple MODY Genes in 58 Italian Families Recruited in the Pediatric or Adult Diabetes Clinic From a Single Italian Hospital

M. Carella, R. Di Paola, L. Zelante, 2014, Diabetes Care.

Severe insulin resistance in disguise: A familial case of reactive hypoglycemia associated with a novel heterozygous INSR mutation

S. Bernardini, F. Barbetti, V. Grasso, 2018, Pediatric diabetes.

Permanent diabetes during the first year of life: multiple gene screening in 54 patients

F. Cerutti, L. Aguilar-Bryan, M. Stazi, 2011, Diabetologia.

Neonatal Diabetes: Permanent Neonatal Diabetes and Transient Neonatal Diabetes

P. Arvan, C. Nichols, M. Remedi, 2017 .

Functional Characterization of a Novel KCNJ11 in Frame Mutation-Deletion Associated with Infancy-Onset Diabetes and a Mild Form of Intermediate DEND: A Battle between KATP Gain of Channel Activity and Loss of Channel Expression

Anlong Li, C. Nichols, A. Crinò, 2013, PloS one.

Glyburide ameliorates motor coordination and glucose homeostasis in a child with diabetes associated with the KCNJ11/S225T, del226‐232 mutation

E. Mercuri, C. Nichols, S. Ricci, 2012, Pediatric diabetes.

Differences between Transient Neonatal Diabetes Mellitus Subtypes can Guide Diagnosis and Therapy.

G. d’Annunzio, V. Calcaterra, A. Novelli, 2021, European journal of endocrinology.

Diabetes associated with dominant insulin gene mutations: outcome of 24-month, sensor-augmented insulin pump treatment

C. Cortese, F. Barbetti, V. Grasso, 2015, Acta Diabetologica.

A possible role of transglutaminase 2 in the nucleus of INS-1E and of cells of human pancreatic islets

S. Petrini, F. Bertuzzi, M. Alessio, 2014, Journal of proteomics.

Permanent diabetes during the first year of life: multiple gene screening in 54 patients

M. Stazi, V. Grasso, R. Pesavento, 2011, Diabetologia.