• 8430 Citations
  • 52 h-Index
1989 …2019
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Fingerprint Dive into the research topics where Luca Persani is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 22 Similar Profiles
Thyroid Gland Medicine & Life Sciences
Mutation Medicine & Life Sciences
Thyrotropin Medicine & Life Sciences
Congenital Hypothyroidism Medicine & Life Sciences
Hypothyroidism Medicine & Life Sciences
Pituitary Neoplasms Medicine & Life Sciences
Thyroid Hormone Resistance Syndrome Medicine & Life Sciences
Thyrotropin Receptors Medicine & Life Sciences

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Research Output 1989 2019

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
5 Citations (Scopus)

2018 European Thyroid Association (ETA) Guidelines on the Diagnosis and Management of Central Hypothyroidism

Persani, L., Brabant, G., Dattani, M., Bonomi, M., Feldt-Rasmussen, U., Fliers, E., Gruters, A., Maiter, D., Schoenmakers, N. & Paul Van Trotsenburg, A. S., Oct 1 2018, In : European Thyroid Journal. 7, 5, p. 225-237 13 p.

Research output: Contribution to journalReview article

Hypothyroidism
Guidelines
Advisory Committees
Thyroid Gland
Expert Testimony
1 Citation (Scopus)

A balanced reciprocal translocation t(10;15)(q22.3;q26.1) interrupting ACAN gene in a family with proportionate short stature

Crippa, M., Giangiobbe, S., Villa, R., Bestetti, I., De Filippis, T., Fatti, L., Taurino, J., Larizza, L., Persani, L., Bellini, F., Finelli, P. & Bonati, M. T., Aug 1 2018, In : Journal of Endocrinological Investigation. 41, 8, p. 929-936 8 p.

Research output: Contribution to journalArticle

Phenotype
Genes
Growth
Osteochondritis Dissecans
Haploinsufficiency
13 Citations (Scopus)

Advances in the Molecular Pathophysiology, Genetics, and Treatment of Primary Ovarian Insufficiency

Huhtaniemi, I., Hovatta, O., La Marca, A., Livera, G., Monniaux, D., Persani, L., Heddar, A., Jarzabek, K., Laisk-Podar, T., Salumets, A., Tapanainen, J. S., Veitia, R. A., Visser, J. A., Wieacker, P., Wolczynski, S. & Misrahi, M., Jun 1 2018, In : Trends in Endocrinology and Metabolism. 29, 6, p. 400-419 20 p.

Research output: Contribution to journalReview article

Primary Ovarian Insufficiency
Molecular Biology
Genes
Fertility Preservation
Genetic Heterogeneity

A novel IGSF1 mutation in a large Irish kindred highlights the need for familial screening in the IGSF1 deficiency syndrome

Roche, E. F., McGowan, A., Koulouri, O., Turgeon, M. O., Nicholas, A. K., Heffernan, E., El-Khairi, R., Abid, N., Lyons, G., Halsall, D., Bonomi, M., Persani, L., Dattani, M. T., Gurnell, M., Bernard, D. J. & Schoenmakers, N., Dec 1 2018, In : Clinical Endocrinology. 89, 6, p. 813-823 11 p.

Research output: Contribution to journalArticle

Congenital Hypothyroidism
Mutation
Neonatal Jaundice
Pituitary Hormones
Penetrance