๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Cover of Kenny and the Dragon

Kenny and the Dragon

โœ Scribed by Tony DiTerlizzi


Publisher
Simon & Schuster Books for Young Readers
Year
2012
Tongue
English
Weight
910 KB
Edition
1st Simon & Schuster books for Young Reader pbk. ed
Category
Fiction
City
New York
ISBN
1442436514

No coin nor oath required. For personal study only.

โœฆ Synopsis


Now in paperback, the New York Times bestselling tale of chivalry and showmanship from Tony DiTerlizzi.

Kenny is a little rabbit with a very big problem. His two best friends are heading into a battle of legendary proportions--with each other! In one corner there's Graeme, a well-read and cultured dragon with sophisticated tastes. In the other there's George, a retired knight and dragon slayer who would be content to spend the rest of his days in his bookshop. Neither really wants to fight, but the village townsfolk are set on removing Graeme from their midst and calling George out of retirement. Can Kenny avert disaster?

Tony DiTerlizzi puts a fun-filled, thoroughly theatrical spin on Kenneth Graeme's classic tale of subterfuge and showmanship with this lighthearted romp of a retelling.

โœฆ Subjects


Rabbits -- Fiction


๐Ÿ“œ SIMILAR VOLUMES


Kenny
โœ Sheckley, Robert ๐Ÿ“‚ Fiction ๐Ÿ“… 0 ๐ŸŒ English โš– 5 KB
Kenny and religious experience
โœ Jeff Jordan ๐Ÿ“‚ Article ๐Ÿ“… 1990 ๐Ÿ› Springer Netherlands ๐ŸŒ English โš– 468 KB
Kenny and sensing God
โœ Charles Taliaferro ๐Ÿ“‚ Article ๐Ÿ“… 1986 ๐Ÿ› Springer Netherlands ๐ŸŒ English โš– 295 KB
Kenny Ausubel
๐Ÿ“‚ Fiction ๐Ÿ“… 2012 ๐ŸŒ English โš– 2 MB
Kenny-Caffey syndrome and microorchidism
โœ Hoffman, William H.; Kovacs, Kalman; Li, Shibo; Kulharya, Anita S.; Johnson, Bru ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 32 KB

We report on two adolescent boys with Kenny-Caffey syndrome and microorchidism. The first patient had elevated levels of serum follicle-stimulating hormone, but normal levels of luteinizing hormone and testosterone. There was no evidence of a microdeletion of the Y chromosome. The second patient had