20182019
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Fingerprint Dive into the research topics where Anna Elsa Maria Allegri is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 6 Similar Profiles
Pituitary Gland Medicine & Life Sciences
Pituitary Diseases Medicine & Life Sciences
Adrenal Insufficiency Medicine & Life Sciences
Mutation Medicine & Life Sciences
Gadolinium Medicine & Life Sciences
Hydrocephalus Medicine & Life Sciences
Phenotype Medicine & Life Sciences
Haploinsufficiency Medicine & Life Sciences

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Research Output 2018 2019

Accuracy and limitations of the growth hormone (GH) releasing hormone-arginine retesting in young adults with childhood-onset GH deficiency

Patti, G., Noli, S., Capalbo, D., Allegri, A. M. E., Napoli, F., Cappa, M., Ubertini, G. M., Gallizia, A., Notarnicola, S., Ibba, A., Crocco, M., Parodi, S., Salerno, M., Loche, S., Garré, M. L., Tornari, E., Maghnie, M. & Iorgi, N. D., 2019, In : Frontiers in Endocrinology. 10

Research output: Contribution to journalArticle

Pituitary Gland
Haploinsufficiency
Phenotype
Comparative Genomic Hybridization
Neurogenesis

A novel pathogenic MYH3 mutation in a child with Sheldon–Hall syndrome and vertebral fusions

Scala, M., Accogli, A., De Grandis, E., Allegri, A., Bagowski, C. P., Shoukier, M., Maghnie, M. & Capra, V., Mar 1 2018, In : American Journal of Medical Genetics, Part A. 176, 3, p. 663-667 5 p.

Research output: Contribution to journalArticle

Mutation
Arthrogryposis
Muscle Development
Bone Development
Contracture

Central adrenal insufficiency in children and adolescents

Patti, G., Guzzeti, C., Di Iorgi, N., Maria Allegri, A. E., Napoli, F., Loche, S. & Maghnie, M., Aug 1 2018, In : Best Practice and Research: Clinical Endocrinology and Metabolism. 32, 4, p. 425-444 20 p.

Research output: Contribution to journalReview article

Adrenal Insufficiency
Adrenocorticotropic Hormone
Hydrocortisone
Newborn Infant
Pituitary Diseases

Novel CNS malformations and skeletal anomalies in a patient with Beaulieu-boycott-Innes syndrome

Telethon Undiagnosed Diseases Program, Dec 2018, In : American Journal of Medical Genetics, Part A. 176, 12, p. 2835-2840 6 p.

Research output: Contribution to journalArticle

Hydrocephalus
Intellectual Disability
Agenesis of Corpus Callosum
Microcephaly
Mutation