1.
J Pediatr
; 151(3): 319-21, 2007 Sep.
Artículo
en Inglés
| MEDLINE
| ID: mdl-17719948
RESUMEN
Muscle metabolites were obtained by in vivo proton magnetic resonance spectroscopy of 3 patients with Duchenne muscular dystrophy (DMD), 6 patients with spinal muscular atrophy (SMA), and 10 normal volunteers. Patients with DMD and SMA had lower trimethyl amide (TMA)/water and TMA/total creatine (tCr) ratios but normal tCr/water ratios.