ELLI, FRANCESCA MARTA

ELLI, FRANCESCA MARTA  

Dipartimento di Scienze Cliniche e di Comunità  

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Risultati 1 - 20 di 46 (tempo di esecuzione: 0.013 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
Novel pathogenetic variants in PTHLH and TRPS1 genes causing syndromic brachydactyly 2022 F. M. ElliL. FontanaC. AlfieriM. MiozzoM. ArosioG. Mantovani + Article (author) -
The cytoskeleton actin binding protein filamin A impairs both IGF2 mitogenic effects and the efficacy of IGF1R inhibitors in adrenocortical cancer cells 2021 R. CatalanoD. TreppiediF. MangiliF. M. ElliM. ArosioG. MantovaniE. Peverelli + Article (author) -
Pseudohypoparathyroidism: Focus on Cerebral and Renal Calcifications 2021 Mantovani G.Elli F. M. + Article (author) -
Pseudohypoparathyroidism, acrodysostosis, progressive osseous heteroplasia: different names for the same spectrum of diseases? 2021 Elli F. M.Mantovani G. Article (author) -
Recommendations for Diagnosis and Treatment of Pseudohypoparathyroidism and Related Disorders: An Updated Practical Tool for Physicians and Patients 2020 Giovanna MantovaniM. Elli + Article (author) -
Octreotide and pasireotide effects on medullary thyroid carcinoma (MTC) cells growth, migration and invasion 2020 E. GiardinoR. CatalanoF. MangiliA. M. BarbieriD. TreppiediF. M. ElliA. DolciA. SpadaM. ArosioG. MantovaniE. Peverelli + Article (author) -
Unrecognized Pseudohypoparathyroidism Type 1A as a Cause of Hypocalcemia and Seizures in a 64-Year-Old Woman 2019 Elli, Francesca MartaMantovani, Giovanna + Article (author) -
FGF23 and Fetuin-A Interaction and Mesenchymal Osteogenic Transformation 2019 Ikehata, MasamiAlfieri, Carlo M.Barilani, MarioElli, Francesca M.Mantovani, GiovannaMessa, Piergiorgio + Article (author) -
Inactivating PTH/PTHrP Signaling Disorders 2019 Mantovani, GiovannaElli, Francesca M. Book Part (author) -
Hypercalcitoninaemia in pseudohypo-parathyroidism type 1A and type 1B 2019 Elli, Francesca MartaMantovani, Giovanna + Article (author) -
Improved Molecular Diagnosis of McCune-Albright Syndrome and Bone Fibrous Dysplasia by Digital PCR 2019 F. M. ElliM. A. MaffiniA. PirelliM. ArosioG. Mantovani + Article (author) -
Association of GNAS Imprinting Defects and Deletions of Chromosome 2 in Two Patients : Clues Explaining Phenotypic Heterogeneity in Pseudohypoparathyroidism Type 1B/iPPSD3 2019 F. M. ElliM. A. MaffiniA. PirelliM. ArosioG. Mantovani + Article (author) -
2q37 Deletions in Patients With an Albright Hereditary Osteodystrophy Phenotype and PTH Resistance 2019 F. M. ElliM. A. MaffiniA. PirelliM. ArosioG. Mantovani + Article (author) -
Genetic and epigenetic defects at the GNAS locus lead to distinct patterns of skeletal growth but similar early-onset obesity 2018 Elli FMantovani G + Article (author) -
Mosaicism for GNAS methylation defects associated with pseudohypoparathyroidism type 1B arose in early post-zygotic phases 2018 F. ElliM. ArosioA. SpadaG. Mantovani + Article (author) -
Diagnosis and management of pseudohypoparathyroidism and related disorders: First international Consensus Statement 2018 Mantovani, GiovannaElli, Francesca M. + Article (author) -
Parathyroid hormone resistance syndromes – Inactivating PTH/PTHrP signaling disorders (iPPSDs) 2018 Elli, Francesca MartaMantovani, Giovanna + Article (author) -
Multiple hormone resistance and alterations of GPCRs signaling 2018 G. MantovaniF. M. Elli Article (author) -
Hypothyroidism associated with parathyroid disorders 2017 G. MantovaniF. M. ElliS. Corbetta Article (author) -
Fibrocartilaginous mesenchymoma of bone: a single-institution experience with molecular investigations and a review of the literature 2017 Elli, Francesca MMantovani, Giovanna + Article (author) -