• 4994 Citations
  • 39 h-Index
1985 …2019
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Fingerprint Dive into the research topics where Mohamad Maghnie is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 17 Similar Profiles
Growth Hormone Medicine & Life Sciences
Neurogenic Diabetes Insipidus Medicine & Life Sciences
Pituitary Gland Medicine & Life Sciences
Magnetic Resonance Imaging Medicine & Life Sciences
Hypopituitarism Medicine & Life Sciences
Insulin-Like Growth Factor I Medicine & Life Sciences
Pituitary Dwarfism Medicine & Life Sciences
Growth Medicine & Life Sciences

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Research Output 1985 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. & Di Iorgi, N., 2019, In : Frontiers in Endocrinology. 10, p. 525

Research output: Contribution to journalArticle

Growth Hormone-Releasing Hormone
Growth Hormone
Arginine
Young Adult
Hormones

Familial neurohypophyseal diabetes insipidus in 13 kindreds and 2 novel mutations in the vasopressin gene

Patti, G., Scianguetta, S., Roberti, D., Di Mascio, A., Balsamo, A., Brugnara, M., Cappa, M., Casale, M., Cavarzere, P., Cipriani, S., Corbetta, S., Gaudino, R., Iughetti, L., Martini, L., Napoli, F., Peri, A., Salerno, M., Salerno, R., Passeri, E., Maghnie, M. & 2 others, Perrotta, S. & Di Iorgi, N., Jun 1 2019, In : European Journal of Endocrinology.

Research output: Contribution to journalArticle

Neurogenic Diabetes Insipidus
Vasopressins
Arginine Vasopressin
Mutation
Genes

X-linked hypophosphatemic rickets: an Italian experts' opinion survey

Emma, F., Cappa, M., Antoniazzi, F., Bianchi, M. L., Chiodini, I., Eller Vainicher, C., Di Iorgi, N., Maghnie, M., Cassio, A., Balsamo, A., Baronio, F., de Sanctis, L., Tessaris, D., Baroncelli, G. I., Mora, S., Brandi, M. L., Weber, G., D'Ausilio, A. & Lanati, E. P., May 31 2019, In : Italian Journal of Pediatrics. 45, 1, p. 67

Research output: Contribution to journalArticle

Familial Hypophosphatemic Rickets
Expert Testimony
Tooth
Growth Disorders
Nephrocalcinosis

X-linked hypophosphatemic rickets: An Italian experts' opinion survey

Emma, F., Cappa, M., Antoniazzi, F., Bianchi, M. L., Chiodini, I., Eller Vainicher, C., Di Iorgi, N., Maghnie, M., Cassio, A., Balsamo, A., Baronio, F., De Sanctis, L., Tessaris, D., Baroncelli, G. I., Mora, S., Brandi, M. L., Weber, G., D'Ausilio, A. & Lanati, E. P., May 31 2019, In : Italian Journal of Pediatrics. 45, 1, 67.

Research output: Contribution to journalArticle

Open Access
Familial Hypophosphatemic Rickets
Expert Testimony
Tooth
Growth Disorders
Nephrocalcinosis
2 Citations (Scopus)

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