hypertrophic cardiomyopathy

Cardiopatia ipertrofica ostruttiva transitoria indotta da steroide: un caso oltre l'età neonatale

La Malfa G, Barbera G, Saia GF, Cardillo M, Scardino G, Sanfilippo MF, Comparato C

2026/2 — pag. 30-34 — DOI

Steroid-induced hypertrophic cardiopathy is a rare and transient condition, predominantly described in neonates receiving corticosteroid therapy for respiratory diseases. Although several case reports exist in literature, this clinical entity is poor...

Infezioni rare del flusso sanguigno correlate a catetere: coinvolgimento insolito di batteri tipicamente non patogeni in un caso pediatrico. Come trattare?

Barbera G, La Malfa G, Saia GF, Cardillo M, Sanfilippo MF, Comparato C

2025/10 — pag. 260-263 — DOI

Rothia dentocariosa, a commensal organism of the oral cavity, is an uncommon pathogen that predominantly affects immunocompromised individuals or patients with indwelling medical devices. The paper reports a case of Rothia dentocariosa catheter-relat...

La sindrome di Noonan

Scupilliti S, Cianci P, Mariani M, Selicorni A.

2023/10 — pag. 657-659 — DOI

Un minestrone preparato con il cuore

A. Iacono

2019/7 — pag. 449-451

Diagnosi di malattia di Pompe nel neonato

C. Amador, M. Sacchini, E. Agostini, E. Procopio, E. Laudani, P. Fiorini

2014/6 — pag. 397-399

Pompe disease is an autosomal recessive storage disorder caused by a deficiency in the enzyme α-glucosidase, resulting in intralysosomal glycogen accumulation in skeletal and cardiac muscle. The classic infantile form is characterized by progres...

Diagnosi di malattia di Pompe nel neonato

C. Amador, M. Sacchini, E. Agostini, E. Procopio, E. Laudani, P. Fiorini

2014/6

Pompe disease is an autosomal recessive storage disorder caused by a deficiency in the enzyme α-glucosidase, resulting in intralysosomal glycogen accumulation in skeletal and cardiac muscle. The classic infantile form is characterized by progres...

La sindrome di Noonan

2012/3 — pag. 190-191

Sindrome di Noonan, associata a celiachia e a cardiomiopatia

A. Borrelli, A. Correra, D. Ummarino, M. Ummarino

2009/1