Diagnostic value of muscle MRI in differentiating LGMD2I from other LGMDs
- 23 February 2005
- journal article
- research article
- Published by Springer Science and Business Media LLC in Zeitschrift für Neurologie
- Vol. 252 (5), 538-547
- https://doi.org/10.1007/s00415-005-0684-4
Abstract
No abstract availableKeywords
This publication has 27 references indexed in Scilit:
- FKRP (826C>A) frequently causes limb-girdle muscular dystrophy in German patientsJournal of Medical Genetics, 2004
- Loss of Calpain-3 Autocatalytic Activity in LGMD2A Patients with Normal Protein ExpressionThe American Journal of Pathology, 2003
- On symptomatic heterozygous alpha‐sarcoglycan gene mutation carriersAnnals of Neurology, 2003
- Phenotypic spectrum associated with mutations in the fukutin‐related protein geneAnnals of Neurology, 2003
- Consequences of a novel caveolin‐3 mutation in a large German familyAnnals of Neurology, 2003
- A short protocol for muscle MRI in children with muscular dystrophiesEuropean Journal of Paediatric Neurology, 2002
- Post-translational disruption of dystroglycan–ligand interactions in congenital muscular dystrophiesNature, 2002
- Juvenile limb-girdle muscular dystrophyBrain, 1996
- Magnetic resonance imaging of primary skeletal muscle diseases: patterns of distribution and severity of involvementThe British Journal of Radiology, 1990
- AUTOSOMAL RECESSIVE DISTAL MUSCULAR DYSTROPHY AS A NEW TYPE OF PROGRESSIVE MUSCULAR DYSTROPHYBrain, 1986