Showing 1 - 8 results of 8 for search 'Francesca Marta Elli', query time: 0.03s Refine Results
  1. 1
    Mosaicism for GNAS methylation defects associated with pseudohypoparathyroidism type 1B arose in early post-zygotic phases

    Mosaicism for GNAS methylation defects associated with pseudohypoparathyroidism type 1B arose in early post-zygotic phases by Francesca Marta Elli, Paolo Bordogna, Maura Arosio, Anna Spada, Giovanna Mantovani

    Published 2018-02-01
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  2. 2
    Hypercalcitoninaemia in pseudohypoparathyroidism type 1A and type 1B

    Hypercalcitoninaemia in pseudohypoparathyroidism type 1A and type 1B by Maria P Yavropoulou, Efstathios Chronopoulos, George Trovas, Emmanouil Avramidis, Francesca Marta Elli, Giovanna Mantovani, Pantelis Zebekakis, John G Yovos

    Published 2019-01-01
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  3. 3
    Correction to: A complex pheotype in a girl with a novel heterozygous missense variant (p.Ile56Phe) of the GNAS gene

    Correction to: A complex pheotype in a girl with a novel heterozygous missense variant (p.Ile56Phe) of the GNAS gene by Paolo Cavarzere, Andrea Gastaldi, Francesca Marta Elli, Rossella Gaudino, Erika Peverelli, Milena Brugnara, Susanne Thiele, Francesca Granata, Giovanna Mantovani, Franco Antoniazzi

    Published 2022-04-01
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  4. 4
    A complex pheotype in a girl with a novel heterozygous missense variant (p.Ile56Phe) of the GNAS gene

    A complex pheotype in a girl with a novel heterozygous missense variant (p.Ile56Phe) of the GNAS gene by Cavarzere Paolo, Gastaldi Andrea, Francesca Marta Elli, Gaudino Rossella, Peverelli Erika, Brugnara Milena, Susanne Thiele, Granata Francesca, Mantovani Giovanna, Antoniazzi Franco

    Published 2022-02-01
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  5. 5
    2q37 Deletions in Patients With an Albright Hereditary Osteodystrophy Phenotype and PTH Resistance

    2q37 Deletions in Patients With an Albright Hereditary Osteodystrophy Phenotype and PTH Resistance by Francesca Marta Elli, Luisa de Sanctis, Bruno Madeo, Maria A. Maffini, Paolo Bordogna, Arianna Pirelli, Maura Arosio, Maura Arosio, Giovanna Mantovani, Giovanna Mantovani

    Published 2019-08-01
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  6. 6
    Improved Molecular Diagnosis of McCune–Albright Syndrome and Bone Fibrous Dysplasia by Digital PCR

    Improved Molecular Diagnosis of McCune–Albright Syndrome and Bone Fibrous Dysplasia by Digital PCR by Francesca Marta Elli, Luisa de Sanctis, Massimiliano Bergallo, Maria Antonia Maffini, Arianna Pirelli, Ilaria Galliano, Paolo Bordogna, Maura Arosio, Maura Arosio, Giovanna Mantovani, Giovanna Mantovani

    Published 2019-09-01
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  7. 7
    Fibroblast growth factor 23 level modulates the hepatocyte’s alpha-2-HS-glycoprotein transcription through the inflammatory pathway TNFα/NFκB

    Fibroblast growth factor 23 level modulates the hepatocyte’s alpha-2-HS-glycoprotein transcription through the inflammatory pathway TNFα/NFκB by Deborah Mattinzoli, Min Li, Giuseppe Castellano, Giuseppe Castellano, Masami Ikehata, Silvia Armelloni, Francesca Marta Elli, Paolo Molinari, Koji Tsugawa, Carlo Maria Alfieri, Carlo Maria Alfieri, Piergiorgio Messa, Piergiorgio Messa

    Published 2022-12-01
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  8. 8
    Is Encapsulated Medullary Thyroid Carcinoma Associated With a Better Prognosis? A Case Series and a Review of the Literature

    Is Encapsulated Medullary Thyroid Carcinoma Associated With a Better Prognosis? A Case Series and a Review of the Literature by Andrea Contarino, Alessia Dolci, Marco Maggioni, Francesca Maria Porta, Gianluca Lopez, Uberta Verga, Francesca Marta Elli, Elisabetta Francesca Iofrida, Gianmaria Cantoni, Giovanna Mantovani, Giovanna Mantovani, Maura Arosio, Maura Arosio

    Published 2022-04-01
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