Stefania Di Candia

Genetic Analysis of Italian Patients with Congenital Hyperinsulinism of Infancy

Paola Sogno Valin, Maria Carla Proverbio, Cecilia Diceglie et al. · Hormone Research in Paediatrics · 2013 · 554 citations

Life Sciences, Genetics, Pediatrics +16

Persistent mild hypothyroidism associated with novel sequence variants of theDUOX2 gene in two siblings

Maria Cristina Vigone, Laura Fugazzola, I. Zamproni et al. · Human Mutation · 2005 · 117 citations · Full text

Medicine, Endocrinology, Genetics +17

Metabolic syndrome in children with Prader–Willi syndrome: the effect of obesity

Paola Brambilla, Antonino Crinò, Giorgio Bedogni et al. · Nutrition Metabolism and Cardiovascular Diseases · 2010 · 70 citations · Full text

Medicine, Endocrinology, Pediatrics +11

A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver–Russell and Beckwith–Wiedemann syndromes

Silvia Russo, Luciano Calzari, Alessandro Mussa et al. · Clinical Epigenetics · 2016 · 69 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Disorders of glucose metabolism in Prader–Willi syndrome: Results of a multicenter Italian cohort study

Danilo Fintini, Graziano Grugni, Sarah Bocchini et al. · Nutrition Metabolism and Cardiovascular Diseases · 2016 · 67 citations

Life Sciences, Biochemistry, Endocrinology +15