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Fingerprint Dive into the research topics where Maura Arosio is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

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Research Output

2q37 deletions in patients with an albright hereditary osteodystrophy phenotype and PTH resistance

Elli, F. M., de Sanctis, L., Madeo, B., Maffini, M. A., Bordogna, P., Pirelli, A., Arosio, M. & Mantovani, G., Jan 1 2019, In : Frontiers in Endocrinology. 10, AUG, 604.

Research output: Contribution to journalArticle

Open Access
  • A Rare SPRY4 Gene Mutation Is Associated With Anosmia and Adult-Onset Isolated Hypogonadotropic Hypogonadism

    Indirli, R., Cangiano, B., Profka, E., Mantovani, G., Persani, L., Arosio, M., Bonomi, M. & Ferrante, E., Nov 12 2019, In : Frontiers in Endocrinology. 10, 781.

    Research output: Contribution to journalArticle

    Open Access
  • Arthropathy in acromegaly: a questionnaire-based estimation of motor disability and its relation with quality of life and work productivity

    The Study Group on Motor Disability in Acromegaly of the Italian Society of Endocrinology, Oct 1 2019, In : Pituitary. 22, 5, p. 552-560 9 p.

    Research output: Contribution to journalArticle

  • Arthropathy in acromegaly: a questionnaire-based estimation of motor disability and its relation with quality of life and work productivity

    Study Group on Motor Disability in Acromegaly of the Italian Society of Endocrinology, Oct 2019, In : Pituitary. 22, 5, p. 552-560 9 p.

    Research output: Contribution to journalArticle