I. Zamproni

发表

Pediatric HIV infection and bone health: an emerging challenge.

G. Zuccotti, S. Mora, A. Viganò, 2010, Frontiers in bioscience.

Analysis of Bone Mineral Content in Horizontally HIV-Infected Children Naïve to Antiretroviral Treatment

S. Mora, V. Giacomet, A. Viganò, 2005, Calcified Tissue International.

Genetic defects of hydrogen peroxide generation in the thyroid gland

L. Fugazzola, G. Weber, I. Zamproni, 2013, Journal of Endocrinological Investigation.

Biallelic inactivation of the dual oxidase maturation factor 2 (DUOXA2) gene as a novel cause of congenital hypothyroidism.

L. Persani, S. Mora, S. Refetoff, 2008, The Journal of clinical endocrinology and metabolism.

The clinical and molecular characterization of patients with dyshormonogenic congenital hypothyroidism reveals specific diagnostic clues for DUOX2 defects.

P. Beck‐Peccoz, L. Beccaria, L. Persani, 2014, The Journal of clinical endocrinology and metabolism.

Identification of a novel polymorphism in the fibronectin type II domain of the SEL1L gene and possible relation to the persistent hyperinsulinemic hypoglycemia of infancy.

D. Antonello, P. Moore, I. Biunno, 2004, Mutation research.

Identification of two novel frameshift mutations in the KCNJ11 gene in two Italian patients affected by Congenital Hyperinsulinism of Infancy.

C. Doglioni, I. Biunno, L. Albarello, 2007, Experimental and molecular pathology.

Alterations in circulating osteoimmune factors may be responsible for high bone resorption rate in HIV-infected children and adolescents

P. Erba, G. Zuccotti, S. Mora, 2007, AIDS.

Persistent mild hypothyroidism associated with novel sequence variants of the DUOX2 gene in two siblings

L. Persani, G. Chiumello, L. Fugazzola, 2005, Human mutation.

Autosomal Dominant Hypocalcemia in Monozygotic Twins Caused by a De Novo Germline Mutation Near the Amino‐Terminus of the Human Calcium Receptor

S. Mora, A. Spiegel, Jianxin Hu, 2004, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Differential effect of age, gender and puberty on bone formation rate assessed by measurement of bone-specific alkaline phosphatase in healthy Italian children and adolescents

P. Erba, S. Mora, V. Giacomet, 2009, Journal of Bone and Mineral Metabolism.

Genetic Analysis of Italian Patients with Congenital Hyperinsulinism of Infancy

A. Salvatoni, C. Battaglia, S. Mora, 2013, Hormone Research in Paediatrics.

Tenofovir Disoproxil Fumarate and Bone Mineral Density: A 60-Month Longitudinal Study in a Cohort of H V -Infected Youths

V. Fabiano, G. Zuccotti, C. Cerini, 2010, Antiviral therapy.

Longitudinal changes of bone mineral density and metabolism in antiretroviral-treated human immunodeficiency virus-infected children.

R. Bianchi, S. Mora, V. Giacomet, 2004, The Journal of clinical endocrinology and metabolism.

Pseudohypoparathyroidism, an often delayed diagnosis: a case series

S. Mora, G. Chiumello, G. Weber, 2009, Cases journal.

Congenital hypothyroidism with eutopic thyroid gland: analysis of clinical and biochemical features at diagnosis and after re-evaluation.

L. Persani, G. Chiumello, L. Fugazzola, 2013, The Journal of clinical endocrinology and metabolism.

Whole Genome SNP Genotyping and Exome Sequencing Reveal Novel Genetic Variants and Putative Causative Genes in Congenital Hyperinsulinism

A. Salvatoni, C. Battaglia, G. De Bellis, 2013, PloS one.

Severe hypocalcemia due to a de novo mutation in the fifth transmembrane domain of the calcium‐sensing receptor

S. Mora, G. Chiumello, G. Weber, 2006, American journal of medical genetics. Part A.

Normalization of Fat Accrual in Lipoatrophic, HIV-Infected Children Switched from Stavudine to Tenofovir and from Protease Inhibitor to Efavirenz

P. Brambilla, G. Zuccotti, S. Mora, 2006, Antiviral therapy.

The Clinical and Molecular Characterization of Patients With Dyshormonogenic Congenital Hypothyroidism Reveals Specific Diagnostic Clues for DUOX 2 Defects

P. Beck‐Peccoz, L. Beccaria, L. Persani, 2014 .