Genes, Neoplasm

Displasia ossea con scarsa crescita

A. Trombetta

2020/10 — pag. 257-258 — DOI

A case of a short girl affected by multiple familial osteochondrosis (MFO) is described. The Author underlines the need of a strict, long term clinical monitoring in all MFO children and in their affected parents because of a significantly increased ...

La sindrome del carcinoma nevoide a cellule basali o sindrome di Gorlin-Goltz

A. Agrusti

2018/3 — pag. 184-185

Storia di nei che parlavano di intestino

I. Festa, R. Caiazzo, S. Napodano, C. Coppola, L. Sessa, E. De Nitto, P. Marzuillo, C. Strisciuglio, L. Perrone

2017/5

Il retinoblastoma

A. D’Ambrosio, G. Coriolani, M. Caini, D. Galimberti, S. Giomi, S. Badii, S. Moretti, M.S. Toti, F. Coccina, F. Carra, T. Hadjistilianou

2013/4 — pag. 227-236

Retinoblastoma is the most frequently diagnosed intraocular malignancy in infants. Recently, there have been significant advances in the management of this disease. New therapeutic strategies, such as superselective intra-arterial chemotherapy and ...

Questione di... tuberi

L. Matarazzo

2012/7

Oncologia pediatrica: le tappe della diagnosi

P. Paolucci, I. Mariotti, E. Bigi, et al.

2009/2 — pag. 85-93

The objective of cure for more than 70% of children with cancer outlines the successful routes built up by paediatric oncologists over the latest 40 years. This successful story stands for the development and evolution of the diagnostic routes wher...

Neurofibromatosi tipo I (parte prima)

G. Bartolozzi

2009/2

Ipertrofia clitoridea in bambina affetta da neurofibromatosi di tipo 1

E. Ballerini, R. Luksch

2006/9 — pag. 601-602

We report the case of NF1 in a 21 month old female, who presented with hypertrophy of the clitoris. The work-up evaluations revealed the presence of multiple pelvic and abdominal neurofibromas and concomitant histologically assessed presacral ganglio...