Nicoletta Masera
Monza, 20900, Italy
Last Updated: 09/26/2026
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Found 24 publications
Thyroid Function Tests in Children and Adolescents With Trisomy 21: Definition of Syndrome-Specific Reference Ranges.
Journal: The Journal of clinical endocrinology and metabolism
Published: April 11, 2023
Environmental Factors in Northern Italy and Sickle Cell Disease Acute Complications: A Multicentric Study.
Journal: Children (Basel, Switzerland)
Published: August 05, 2022
Acute chest syndrome in children with sickle cell disease: Data from a national AIEOP cohort identify priority areas of intervention in a hub-and-spoke system.
Journal: British journal of haematology
Published: June 28, 2022
Transfusional Approach in Multi-Ethnic Sickle Cell Patients: Real-World Practice Data From a Multicenter Survey in Italy.
Journal: Frontiers in medicine
Published: December 09, 2021
Dexamethasone Stimulation Test in the Diagnostic Work-Up of Growth Hormone Deficiency in Childhood: Clinical Value and Comparison With Insulin-Induced Hypoglycemia.
Journal: Frontiers in endocrinology
Published: August 26, 2020
Hormonal replacement therapy in adolescents and young women with chemo- or radio-induced premature ovarian insufficiency: Practical recommendations.
Journal: Blood reviews
Published: April 02, 2020
The Potential Synergic Effect of a Complex Pattern of Multiple Inherited Genetic Variants as a Pathogenic Factor for Ovarian Dysgenesis: A Case Report.
Journal: Frontiers in endocrinology
Published: March 05, 2020
HbS/β+ thalassemia: Really a mild disease? A National survey from the AIEOP Sickle Cell Disease Study Group with genotype-phenotype correlation.
Journal: European journal of haematology
Published: October 11, 2019
Long-term sequential deferiprone and deferasirox therapy in transfusion-dependent thalassaemia patients: a prospective clinical trial.
Journal: British journal of haematology
Published: July 26, 2019
The use of recombinant human growth hormone in patients with Mucopolysaccharidoses and growth hormone deficiency: a case series.
Journal: Italian journal of pediatrics
Published: March 07, 2019
Evaluation of Technical Issues in a Pilot Multicenter Newborn Screening Program for Sickle Cell Disease.
Journal: International journal of neonatal screening
Published: October 30, 2018
Total loss of GM3 synthase activity by a normally processed enzyme in a novel variant and in all ST3GAL5 variants reported to cause a distinct congenital disorder of glycosylation.
Journal: Glycobiology
Published: October 07, 2018
Last Updated: 09/26/2026