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

  • 31 Similar Profiles
Pseudohypoparathyroidism Medicine & Life Sciences
Pituitary Neoplasms Medicine & Life Sciences
Mutation Medicine & Life Sciences
Filamins Medicine & Life Sciences
Neoplasms Medicine & Life Sciences
Somatostatin Medicine & Life Sciences
Genes Medicine & Life Sciences
Tumors Chemical Compounds

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Research Output 1997 2019

  • 4072 Citations
  • 35 h-Index
  • 188 Article
  • 5 Review article
  • 1 Chapter

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. & 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

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

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