scispace - formally typeset
M

Maria Segni

Researcher at Sapienza University of Rome

Publications -  50
Citations -  2499

Maria Segni is an academic researcher from Sapienza University of Rome. The author has contributed to research in topics: Thyroid & Graves' disease. The author has an hindex of 27, co-authored 50 publications receiving 2322 citations. Previous affiliations of Maria Segni include Maharaja Sayajirao University of Baroda & Policlinico Umberto I.

Papers
More filters
Journal ArticleDOI

Spontaneous Pubertal Development in Turner’s Syndrome

TL;DR: The increased percentage of spontaneous menarche is Turner's syndrome reported in the recent literature might be due to increased ascertainment by diligent screening for Turner’s syndrome in girls with short stature and mild or no Turner's Syndrome stigmata, even though they may be menstruating.
Journal ArticleDOI

Long-term observation of 87 girls with idiopathic central precocious puberty treated with gonadotropin-releasing hormone analogs: impact on adult height, body mass index, bone mineral content, and reproductive function.

TL;DR: GnRHa treatment in ICPP is safe for the reproductive system, BMD, and BMI and helpful in reaching AH close to target height; however, the variability of individual responses suggests that one choose more parameters than increment in height, especially in girls with pubertal onset over 8 yr of age.
Journal ArticleDOI

Accuracy of fine needle aspiration biopsy of thyroid nodules in detecting malignancy in childhood : Comparison with conventional clinical, laboratory, and imaging approaches

TL;DR: Evaluated and compared the diagnostic accuracies of clinical, laboratory, and imaging data collected retrospectively in a group of pediatric patients with thyroid nodules submitted to fine needle aspiration biopsy provides strong evidence that fine needle aspirations biopsy is a safe technique even in childhood and adolescence, offering the best sensitivity, specificity, and accuracy in detecting malignancy compared with conventional approaches.
Journal ArticleDOI

A promoter polymorphism of the CYP27B1 gene is associated with Addison's disease, Hashimoto's thyroiditis, Graves' disease and type 1 diabetes mellitus in Germans

TL;DR: A significant association was found between allelic variation of the promoter (-1260) C/A polymorphism and Addison's disease, Hashimoto's thyroiditis, Graves' disease and type 1 diabetes mellitus, implying a regulatory difference of the CYP27B1 hydroxylase to predispose to endocrine autoimmunity.
Journal ArticleDOI

Special features of Graves' disease in early childhood.

TL;DR: Three unrelated children, all females, in whom GD occurred before the age of 3, presented with goiter, exophthalmos, tachycardia, and hyperactivity, one showed a severe psychomotor delay, and had previously undergone surgery due to craniosynostosis; the other two manifested a language delay.