𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Pathological Evaluation of Renal Tumors in Children: International Society of Pediatric Oncology Approach

✍ Scribed by Liliane A. Boccon-Gibod

Publisher
Springer
Year
1998
Tongue
English
Weight
81 KB
Volume
1
Category
Article
ISSN
1093-5266

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Revised International Society of Paediat
Revised International Society of Paediatric Oncology (SIOP) working classification of renal tumors of childhood
✍ Vujani?, Gordan M. ;Sandstedt, Bengt ;Harms, Dieter ;Kelsey, Anna ;Leuschner, Iv πŸ“‚ Article πŸ“… 2002 πŸ› John Wiley and Sons 🌐 English βš– 102 KB

## Abstract The previous International Society of Paediatric Oncology (SIOP) trials and studies recognized three prognostic groups of renal tumors of childhood: low risk, intermediate risk, and high risk tumors, which were further defined in the SIOP (Stockholm) Working Classification of Renal Tumo

Radiotherapy in the SIOP (international
Radiotherapy in the SIOP (international society of pediatric oncology) nephroblastoma studies: A review
✍ Jereb, Berta ;Burgers, J. Marion V. ;Tournade, Marie-France ;Lemerle, Jean ;Bey, πŸ“‚ Article πŸ“… 1994 πŸ› John Wiley and Sons 🌐 English βš– 543 KB

## Abstract For decades radiation has generally been accepted as a valuable supplement to surgery in the treatment of Wilms' tumor; unfortunately, it may produce undesirable late effects. It turned out, however, that when treatment is adjusted to known variables, the risk for late sequelae can be d

Value of postchemotherapy bioptical veri
Value of postchemotherapy bioptical verification of complete clinical remission in previously incompletely resected (stage I and II pT3) malignant mesenchymal tumors in children: International society of pediatric oncology 1984 malignant mesenchymal tumors study
✍ Godzinski, Jan ;Flamant, FranΓ§oise ;Rey, Annie ;Praquin, Marie-ThΓ©rΓ¨se ;Martelli πŸ“‚ Article πŸ“… 1994 πŸ› John Wiley and Sons 🌐 English βš– 436 KB

## Abstract Bioptical verification of complete clinical remission achieved with postoperative chemotherapy in 140 pediatric patients with nonradically resected stages I and II non‐parameningeal malignant mesenchymal tumors was evaluated. Tumor histology was rhabdomyosarcoma in 92 and nonrhabdomyosa