Rivista di formazione e aggiornamento professionale del pediatra e del medico di base, fondata nel 1982. In collaborazione con l'Associazione Culturale Pediatri.
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Hypopituitarism

13 articoli — 2000-2025

EL I Poster degli specializzandi
Accesso libero
Sfide endocrinologiche neonatali: un caso di ipopituitarismo congenito

Carabelli G, Sala Veni C, Cardani R, Salvatore S, Agosti M

2025/7 — pag. 194-195 — DOI

A full-term newborn delivered by urgent caesarean section developed persistent hypoglycemia within the first hours of life, along with hypotonia, poor feeding and prolonged jaundice. Endocrine evaluation revealed congenital hypopituitarism, confirmed...

EL Caso contributivo
Un caso di ipopituitarismo in età infantile

Guida M, Malizia G, Ferrara D

2023/8 — pag. 146-150 — DOI

Hypopituitarism is often an evolutionary condition, which if not present at birth with the classic signs of severe hypoglycaemia, prolonged jaundice, bilateral cryptorchidism and / or micropenis and alterations of neurological development, causes a d...

EL Il punto su
Il craniofaringioma

Salce N, Giovannelli E, Graziani V, Cozzolino M, Mazzatenta D, Zucchelli M, Marchetti F

2021/7 — pag. 210-216 — DOI

Craniopharyngioma (CP) is a rare epithelial low-grade tumour that develops in the sellar/suprasellar region of the brain, along the craniopharyngeal duct. It has a bimodal distribution and the first peak occurs in paediatric age almost exclusively co...

RI Casi indimenticabili
La fosfatasi alcalina elevata quasi per caso

C. Guiducci, C. Malaventura, G. Maggiore

2018/3 — pag. 192-193

RI Casi indimenticabili
Una cefalea importante

G. Acucella, E. Eljerbi, G. Grugni, A. Guala

2018/3 — pag. 192-193

RI Problemi speciali
Ipopituitarismo congenito

P. Matarazzo, M. Repici, A. Ravaglia

2015/7 — pag. 452-457

A lot of genes govern pituitary gland development, differentiation and function. Mutations in those genes, as well as toxic or infective intrauterine noxae, could derange pituitary gland development, differentiation and function. More precocious is...

RI Aggiornamento monografico
Accesso libero
Il diabete insipido centrale: più luci e meno ombre

M. Maghnie

2001/6 — pag. 361-368

Diabetes insipidus is a multifactorial disease caused by the lack of secretion of vasopressin, its physiologic suppression following excessive water intake, or kidney resistance to its action. The clinical and laboratory diagnosis is confirmed by s...

RI Pagina verde
Accesso libero
Eritromelalgia, vasculite, vitiligo, ipertensione, difetto di gh

R. Cimaz, A. Langer

2000/6 — pag. 391-393

Description of a case of idiopathic erythromelalgia, started at about 5 years, which dramatically developed over many years, with painful crises to the feet (and then also to the hands) mitigated in cold conditions only, with trophic alterations t...