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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Bone Marrow Transplantation

23 articoli — 1997-2025

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...

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...

EL I Poster degli specializzandi
Accesso libero
CAMT: trombocitopenia amegacariocitica congenita

V. Carrato

2020/9 — pag. 239-239 — DOI

EL Caso contributivo
Sindrome da encefalopatia posteriore reversibile. Neurotossicità da ciclosporina

M.V. Abate, A. Proia, A. Locasciulli, A. Ventura

2015/8

Reversible posterior encephalopathy syndrome (PRES) is a clinic-radiologic syndrome characterized by headache, altered mental status, visual and motor symptoms and radiological lesions documented on brain MRI. PRES is characterized by a complete reve...

EL Casi indimenticabili
Al di là dell’occhio!

G. Ferrara, E. Zanelli

2014/3

EL Caso contributivo
Tante visite, una diagnosi “by proxy”: ALPS, la sindrome linfoproliferativa autoimmune

L. Sirianni, M. Mancuso

2013/1

Autoimmune lymphoproliferative syndrome or ALPS is a genetic disease associated with anomalous apoptosis in lymphocytes, lymphoproliferation and autoimmune manifestations. Generally, it is possible to observe severe lymphadenopathy, hepatosplenomegal...

RI Aggiornamento monografico
L'anemia falciforme

M. Lazzerini, M. Rabusin

2006/4 — pag. 223-234

Sickle cell disease (SCD) is one of the most prevalent haemoglobinopathies in the world, being related to areas where malaria is or was endemic. In Italy the majority of patients still live in Sicily, where the overall HbS gene frequency is 2%. Domes...

EL Pediatria per l'ospedale
Accesso libero
ß-talassemia (Parte seconda)

G. Bartolozzi

2006/2

EL Pediatria per immagini
Accesso libero
Polmonite interstiziale in immunodepresso:Il Pneumocisti carinii

M. Lazzerini

2004/10

RI Focus
Che cosa deve sapere il pediatra delle malattie rare

A. Ventura, A. Gagliardo, I. Berti, F. Marchetti

2003/5 — pag. 292

Rare diseases constitute a highly eterogeneous category of (mainly genetic) disorders. Even if the individual diseases are rare, due to their global incidence, rare diseases represent both an important cause of morbidity and mortality and a challen...

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,...

EL Pediatria per l'ospedale
Accesso libero
Le β-talassemie

1999/8

RI Ricerca
Accesso libero
Il trapianto di midollo: un passo avanti per le malattie autoimmuni intrattabili

M. Andolina e coll.

1998/4 — pag. 233-236

We report the results of a series of autologous stem cell transplants in autoimmune diseases. The stem cells were treated ex vivo with vincristine and methylprednisolone as previously in allogeneic mismatched transplants in advanced leukemia. T...