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Luisella Cianferotti

Researcher at University of Florence

Publications -  115
Citations -  3618

Luisella Cianferotti is an academic researcher from University of Florence. The author has contributed to research in topics: Primary hyperparathyroidism & Osteoporosis. The author has an hindex of 29, co-authored 100 publications receiving 2920 citations. Previous affiliations of Luisella Cianferotti include Imperial College London & University of Pisa.

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Surgery or surveillance for mild asymptomatic primary hyperparathyroidism: a prospective, randomized clinical trial.

TL;DR: In patients with mild asymptomatic primary hyperparathyroidism, successful PTx is followed by an improvement in BMD and quality of life, and most patients followed without surgery did not show evidence of progression.
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Genetic analyses of the HRPT2 gene in primary hyperparathyroidism: germline and somatic mutations in familial and sporadic parathyroid tumors.

TL;DR: The finding that two of the seven patients with sporadic parathyroid cancer carried an HRPT2 germline mutation suggests that they might have occult HPT-JT, and the results confirm the need for testingHRPT2 gene in FIHP families.
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A Novel Mutation of the Autoimmune Regulator Gene in an Italian Kindred with Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy, Acting in a Dominant Fashion and Strongly Cosegregating with Hypothyroid Autoimmune Thyroiditis

TL;DR: Analysis of the family tree showed direct transmission of the hypothyroid autoimmune thyroiditis/polyendocrinopathy-candidiasis-ectodermal dystrophy phenotype to the offspring in each generation in the absence of consanguinity, further supporting a dominant inheritance.
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Morphometric vertebral fractures in postmenopausal women with primary hyperparathyroidism.

TL;DR: VF rate is increased in postmenopausal women with PHPT compared to controls, independently of whether they are classified as symptomatic or asymptomatic, and the question of whether the finding of mild morphometric VFs in the latter represents an indication for parathyroid surgery remains to be established.
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Vitamin D receptor is essential for normal keratinocyte stem cell function

TL;DR: Absence of the VDR impairs canonical Wnt signaling in keratinocytes and leads to the development of alopecia due to a defect inkeratinocyte stem cells, as demonstrated by transient gene expression assays.