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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.

  • 34 Similar Profiles
Acromegaly Medicine & Life Sciences
Cushing Syndrome Medicine & Life Sciences
Somatostatin Medicine & Life Sciences
Hydrocortisone Medicine & Life Sciences
Insulin-Like Growth Factor I Medicine & Life Sciences
Growth Hormone Medicine & Life Sciences
Pituitary Neoplasms Medicine & Life Sciences
Therapeutics Medicine & Life Sciences

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Research Output 1978 2019

  • 4672 Citations
  • 42 h-Index
  • 170 Article
  • 5 Review article
  • 1 Letter

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
Phenotype
Pseudohypoparathyroidism
Pseudopseudohypoparathyroidism
Diagnostic Errors
Albright's hereditary osteodystrophy

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, Jan 1 2019, In : Pituitary.

Research output: Contribution to journalArticle

Acromegaly
Joint Diseases
Joints
Quality of Life
Population

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

Fatti, L. M., Cangiano, B., Vitale, G., Persani, L., Mantovani, G., Sala, E., Arosio, M., Maffei, P., Dassie, F., Mormando, M., Giampietro, A., Tanda, L., Masiello, E. R., Nazzari, E., Ferone, D., Corbetta, S., Passeri, E., Guaraldi, F., Grottoli, S., Cannavò, S. & 5 others, Torre, M. L. T., Soranna, D., Zambon, A., Cavagnini, F. & Scacchi, M., 2019, In : Pituitary.

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

Fatti, L. M., Cangiano, B., Vitale, G., Persani, L., Mantovani, G., Sala, E., Arosio, M., Maffei, P., Dassie, F., Mormando, M., Giampietro, A., Tanda, L., Masiello, E. R., Nazzari, E., Ferone, D., Corbetta, S., Passeri, E., Guaraldi, F., Grottoli, S., Cannavò, S. & 6 others, Torre, M. L. T., Soranna, D., Zambon, A., Cavagnini, F., Scacchi, M. & Endocrinology, T. S. G. O. M. D. I. A. O. T. I. S. O., 2019, In : Pituitary. 22, 5, p. 552-560 9 p.

Research output: Contribution to journalArticle

Association of GNAS imprinting defects and deletions of chromosome 2 in two patients: Clues explaining phenotypic heterogeneity in pseudohypoparathyroidism type 1B/iPPSD3

Elli, F. M., Desanctis, L., Maffini, M. A., Bordogna, P., Tessaris, D., Pirelli, A., Arosio, M., Linglart, A. & Mantovani, G., Jan 7 2019, In : Clinical Epigenetics. 11, 1, 2.

Research output: Contribution to journalArticle

Open Access
Chromosomes, Human, Pair 2
Pseudohypoparathyroidism
Brachydactyly
Modifier Genes
Genes