Research Output per year
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
Network
Recent external collaboration on country level. Dive into details by clicking on the dots.
Research Output 1978 2019
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 journal › Article
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 journal › Article
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, , 2019, In : Pituitary.Research output: Contribution to journal › Article
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, , 2019, In : Pituitary. 22, 5, p. 552-560 9 p.Research output: Contribution to journal › Article
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 journal › Article
Open Access
Chromosomes, Human, Pair 2
Pseudohypoparathyroidism
Brachydactyly
Modifier Genes
Genes