Copper

Wilson Wilson Wilson

Carciofi A, Pugliese F, D'alba I, Coccia P, Lionetti ME, Gatti S

2025/5 — pag. 120-121 — DOI

A 13-year-old boy was admitted with abdominal pain, vomiting and unexplained cytopoenia. Initial investigations showed splenomegaly, ileal wall thickening, hepatic structural alterations and persistent pancytopenia. Extensive infectious, haematologic...

Le tre regole di Wilson

A. Lora

2017/3

Insufficienza epatica acuta nel bambino: non è tutto oro... (ma rame)

G. Maggiore, S. Riva, M. Sciveres, F. Cirillo

2014/2

Malattia di Wilson: dieci motivi per (ri)parlarne ai pediatri

R. Iorio, G. Ranucci, D. Liccardo, M.G. Puoti, F. Di Dato

2012/8 — pag. 501-507

Wilson disease (WD) is an inherited autosomal recessive disorder of copper metabolism characterized by progressive copper accumulation in the liver and then in other organs, such as the nervous system, eyes and kidneys. In childhood, clinical prese...

Crederci sempre, arrendersi mai!

G. Maggiore

2006/6 — pag. 385-386

Che strani capelli ha quel bambino?

2004/5 — pag. 326-326

The Authors described a case of a newborn affected by Menkes disease (MNK) with convulsions, connective tissue disorders and hair abnormalities. MNK is an X-linked recessive disorder characterised by a copper-transporting ATPase defect. Subcutaneo...

Che strani capelli ha quel bambino

C. Balducci, A. Vaccaro, E. Spadoni, C. Mazzatenta , L. Luti , L. Matteucci, R. Domenici

2004/4