I. Zamproni

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

Biallelic Inactivation of the Dual Oxidase Maturation Factor 2 (DUOXA2) Gene as a Novel Cause of Congenital Hypothyroidism

I. Zamproni, Helmut Grasberger, Francesca Cortinovis et al. · The Journal of Clinical Endocrinology & Metabolism · 2007 · 181 citations · Full text

Life Sciences, Endocrinology, Genetics +17

Congenital Hypothyroidism With Eutopic Thyroid Gland: Analysis of Clinical and Biochemical Features at Diagnosis and After Re-Evaluation

Sarah Rabbiosi, Maria Cristina Vigone, Francesca Cortinovis et al. · The Journal of Clinical Endocrinology & Metabolism · 2013 · 136 citations · Full text

Medicine, Endocrinology, Endocrine Nuclear Medicine +7

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

Longitudinal Changes of Bone Mineral Density and Metabolism in Antiretroviral-Treated Human Immunodeficiency Virus-Infected Children

Stefano Mora, I. Zamproni, Sabrina Beccio et al. · The Journal of Clinical Endocrinology & Metabolism · 2004 · 108 citations · Full text

Medicine, Infectious Diseases, Bone Metabolism +16