Rivista di formazione e aggiornamento professionale del pediatra e del medico di base, fondata nel 1982. In collaborazione con l'Associazione Culturale Pediatri.
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Genetic Therapy

27 articoli — 2001-2025

RI Protocolli di diagnosi e terapia
Facciamo il punto sull’anemia falciforme

Tessitore A, Cuzzubbo D, Russo G.

2025/5 — pag. 296-298 — DOI

Sickle cell disease (SCD) is an increasingly relevant condition in Italy due to rising immigration from high-prevalence regions. Early diagnosis through newborn screening and comprehensive management - including hydroxyurea, antibiotic prophylaxis, t...

EL Caso contributivo
Una strana pancitopenia: dalla gestione in urgenza alla diagnosi genetica

Di Filippo M, Rossoni L, Nebiolo M, Fioredda F, Carrato V, Pirlo D

2024/10 — pag. 201-206 — DOI

Wiskott-Aldrich syndrome (WAS) is a rare X-linked genetic disorder caused by a mutation in the WAS gene that codes for the WASp protein, which is involved in the functioning of the cytoskeleton of non-erythroid haematopoietic cells. This mutation lea...

RI Aggiornamento
Difetti congeniti dell’immunità: non solo le vecchie immunodeficienze

Tommasini A, Valencic E, Naviglio S.

2024/4 — pag. 219-226 — DOI

Inborn errors of immunity are a rapidly-developing area of clinical study. Based on the description of a small set of disorders with a significant risk of infection that may be identified with a small number of lab tests, the definition has been expa...

RI Editoriali
Il farmaco più costoso del mondo

Guala A, Parodi E.

2023/7 — pag. 415-416 — DOI

RI Casi indimenticabili
La storia dell’atrofia muscolare spinale: questione di tempo

Sutera M, Bruno I

2022/4 — pag. 255-258 — DOI

The authors present the case of a girl diagnosed with spinal muscular atrophy (SMA) and discuss how the new therapeutic approaches may change the prospect of life of the affected patients....

RI Speciale
Malattie rare

Bruno I, Selicorni A

2021/26 — pag. 7 — DOI

RI Il graffio
Le larghe spalle della pediatria

2018/2 — pag. 81

RI Aggiornamento
Distrofia muscolare di Duchenne:stato dell’arte su nuovi approcci terapeutici

S. Messina, E. Mercuri

2016/9 — pag. 565-571

Duchenne muscular dystrophy is an X-linked disorder with an incidence of 1 in 5,000 male live births and is the most common muscular dystrophy in childhood. The disease is characterized by progression of muscle weakness and contractures leading to ...

RI Aggiornamento
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...

RI Focus
Prospettive di nuove terapie della fibrosi cistica

M. Conese, L. Palmieri, E. Copreni

2006/3 — pag. 155-173

Although to date symptomatic therapies for cystic fibrosis (CF) - based on the eradication/ control of opportunistic infections and facilitation of mucus excretion - have rapidly and significantly increased patients survival, an aetiological therapy ...

RI Aggiornamento
Gen-Etica: di chi sono i geni?

B. Dallapiccola

2003/9 — pag. 575-580

The Author offers an overview of all the main ethical issues related to the recent advances of genetics. Special attention is paid to the following: options in assisted fertilization, recent developments in our understanding of genetic basis of dis...

EL Appunti di Terapia
Accesso libero
Vettori virali per il trasferimento di geni

G. Bartolozzi

2001/3

RI Focus
Accesso libero
I geni della malattia: la cura delle malattie genetiche

L.D. Notarangelo

2001/1 — pag. 24-29

The treatment of genetic diseases is not fruit of the imagination, although too many hasty statements, such as those on gene therapy, created a deep disappointment. Effective medical actions include marrow grafting, replacement treatments (enzymes,...