nefrocalcinosi

Non ti scordar del tubulo: la malattia di Dent

Benvenuto S, Bossini B

2022/5 — pag. 112-112 — DOI

The case of a 12-year-old boy with proteinuria, microhaematuria and nephrocalcinosis with normal glomerular function is described. A diagnosis of Dent disease was eventually made and confirmed by the genetic test....

Rachitismo ipofosforemico X-linked

L. Lucchetti, D. Fintini, M. Cappa, F. Emma

2020/7 — pag. 430-436 — DOI

X-linked hypophosphatemia (XLH) is an X-linked disorder with dominant penetration, caused by mutations in the PHEX gene, which encodes for an endopeptidase that is predominantly expressed in osteoblasts, osteocytes and odontoblasts. PHEX mutations ...

Nefrocalcinosi e gene SLC34A1

M. Luzzati

2020/2 — pag. 39-39

Non è sempre colpa della mamma!

G. Ferrara

2015/2

Nefrocalcinosi da povertà

E. Zanelli, P. Tommasi, M. Della Rocca, G. Zuin, M. Frediani, M. Fontana

2014/9

Vitamina D: è indispensabile... ma non esageriamo!

E.M.G. Marrella, S.Tagliati, S. Brachi, C. Gelli, M. Giovannini, G. Turlà, C. Malaventura

2013/8

The article presents a case of severe hypercalcemia due to hypervitaminosis D in a 5-month-old infant. The child was fed with infant formula. He received 2 drops of 25-hydroxy vitamin D3/day since he was born. His clinical features showed growth reta...

Un buon motivo per non crescere

G. Gortani, A. Tado, A. Amaddeo, V. Kiren, E. Barbi, F. Marchetti

2007/2

Nefrocalcinosi in lattante: ipersensibilita' alla vitamina D

A. Bertinelli

2000/7