cardiomyopathies

Shock da paura: quando è il feocromocitoma a far battere il cuore

Carbonara L, Romaniello M, Grutter G

2026/3 — pag. 75-76 — DOI

Pheochromocytoma is a rare neuroendocrine tumour in children that typically presents with hypertension but may lead to life-threatening complications. The paper reports the case of a 12-year-old boy presenting with cardiogenic shock and severe left v...

ARPKD: una malattia clinicamente eterogenea che richiede un approccio terapeutico multidisciplinare

E. Petrucci

2018/5

Nuovi concetti nel campo della distrofia muscolare di Duchenne

M. Pane, F. Bianco, C. Palermo, A. Graziano, E. Mercuri

2012/7 — pag. 429-435

Duchenne muscular dystrophy has an incidence of 1 in 3,500 male live births and is the most common muscular dystrophy in childhood. The “typical” course of the disease is characterized by progression of muscle weakness and contractures leading to l...

Distrofia muscolare di Duchenne: si può fare di più

2010/10 — pag. 663-664

Maremoto

F. Panizon

2005/1 — pag. 9

Le urgenze cardiologiche in età perinatale Parte II

U. Vairo, et al.

2004/5 — pag. 293-300

Continued postnatal development of the conduction system and of the sympathetic nervous system of the heart may predispose the newborn to arrhythmias and conduction disturbances that are not seen in older children. In addition, unfavorable environm...

Un caso di ipertransaminasemia

M. Lazzerini

2003/8

La malattia di Anderson-Fabry in età pediatrica

V.I. Guerci, M.G. Pittis, G. Ciana, et al.

2003/5 — pag. 309

Fabry disease is an X-linked, recessive inborn error of glycosphingolipid metabolism resulting from deficient alpha-galactosidase A activity. The codifying gene has been mapped in position Xq22.1 and more than 150 mutations are known, most of them ...