Elisabetta Lapi
Florence, 50139, Italy
Last Updated: 09/26/2026
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Found 21 publications
Mosaic Segmental and Whole-Chromosome Upd(11)mat in Silver-Russell Syndrome.
Journal: Genes
Published: March 15, 2021
Excess of de novo variants in genes involved in chromatin remodelling in patients with marfanoid habitus and intellectual disability.
Journal: Journal of medical genetics
Published: July 16, 2019
Bone Status in a Patient with Insulin-Like Growth Factor-1 Receptor Deletion Syndrome: Bone Quality and Structure Evaluation Using Dual-Energy X-Ray Absorptiometry, Peripheral Quantitative Computed Tomography, and Quantitative Ultrasonography.
Journal: Frontiers in endocrinology
Published: January 07, 2017
Bone mineral status and metabolism in patients with Williams-Beuren syndrome.
Journal: Hormones (Athens, Greece)
Published: February 16, 2016
Bone Mineral Status in Children and Adolescents with Klinefelter Syndrome.
Journal: International journal of endocrinology
Published: January 17, 2016
Epigenetic control of the immune system: a lesson from Kabuki syndrome.
Journal: Immunologic research
Published: September 29, 2015
Triple X syndrome and puberty: focus on the hypothalamus-hypophysis-gonad axis.
Journal: Fertility and sterility
Published: September 09, 2015
Giant multiple bladder diverticula in Williams-Beuren syndrome.
Journal: Kidney international
Published: August 01, 2015
Bone status in genetic syndromes: a review.
Journal: Hormones (Athens, Greece)
Published: April 18, 2015
Agenesis of internal carotid artery associated with isolated growth hormone deficiency: a case report and literature review.
Journal: BMC endocrine disorders
Published: February 25, 2015
Last Updated: 09/26/2026