Bone Diseases, Metabolic

Un varismo che fa rima con…

Zampieri A, Corona F, Magnolato A, Barbi E.

2024/6 — pag. 383-385 — DOI

The paper reports the case of a 1-year-old girl with evident genu varum, frontal bossing, anterior bowing of tibia and mother’s history of short stature treated in infancy with GH. Biochemical findings show increased alkaline phosphatase and hypophos...

Una fosfatasi alcalina non fa rachitismo

Ballaben A

2023/9 — pag. 601-604 — DOI

The case of an 18-month-old asymptomatic girl with isolated high alkaline phosphatase blood levels is described. The diagnosis of benign, transient hyperphosphatasemia was finally made....

Frattura e rachitismo in un’adolescente

Pacenti E, Lazzari M, Pugliese F

2023/3 — pag. 50-50 — DOI

The diagnosis of vitamin D deficiency (rickets) was finally made in a 13-year-old Pakistani girl who had fallen victim of bullying and social isolation during lockdown and who presented with multiple osteolytic femoral lesions....

Farmaci antiepilettici, vitamina D e mineralizzazione ossea: le evidenze e le azioni

Troisi A, Lama C, Iacono A, Ricciardelli P, Marchetti F

2021/4 — pag. 258-260 — DOI

The possible negative effects of antiepileptic drugs on bone metabolism with the consequent possible risks have been discussed in the literature for more than 30 years. Two reviews of the literature attempted to answer the following clinical question...

Farmaci antiepilettici, vitamina D e mineralizzazione ossea: le evidenze e le azioni

Troisi A, Lama C, Iacono A, Ricciardelli P, Marchetti F

2021/4 — pag. 124-128 — DOI

The possible negative effects of antiepileptic drugs on bone metabolism with the consequent possible risks have been discussed in the literature for more than 30 years. Two reviews of the literature attempted to answer the following clinical question...

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 ...

Il neonato a colori: le sfumature di grigio

G. Corsello, M. Schierz

2019/7 — pag. 455-456

Quali malattie sono legate al deficit di vitamina D?

V. Murgia

2015/8 — pag. 531-532

Nefrocalcinosi da povertà

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

2014/9

Dolori senza dottori: la gestione del dolore nei bambini con gravi deficit cognitivi

M. Massaro, G. Pisciotta, P. Vallon, E. Barbi, A. Ventura

2012/5 — pag. 307-313

Pain is a frequent and relevant problem in children with severe cognitive impairments, but it is often underrated and therefore undertreated. A good pain management for these patients requires the use of specific validated pain scales, in order to ...

L’iperfosfatasemia transitoria dei lattanti sani

G. Bartolozzi

2009/9

C’è ancora!

M. Porrello, D. Corso

1998/5 — pag. 326