𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Cerebellar hematoma in a carrier of the A3243G MELAS mutation

✍ Scribed by E. Saracchi; L. Tremolizzo; J. C. DiFrancesco; L. Brighina; G. Costantino; B. Frigeni; M. Brioschi; M. L. Piatti; L. Fumagalli; L. Marzorati; N. A. Curtò; C. Ferrarese


Book ID
106269110
Publisher
Springer Milan
Year
2011
Tongue
English
Weight
94 KB
Volume
32
Category
Article
ISSN
1590-1874

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Oxidative phosphorylation defect in the
✍ François Dubeau; Nicola De Stefano; Benjamin G. Zifkin; Douglas L. Arnold; Eric 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 312 KB

MELAS is a mitochondrial encephalomyopathy characterized clinically by recurrent stroke-like episodes, seizures, sensorineural deafness, dementia, hypertrophic cardiomyopathy, and short stature. The majority of patients are heteroplasmic for a mutation (A3243G) in the tRNA leu(UUR) gene in mitochond