Proximal myopathy and diffuse white matter involvement in myotonic dystrophy type I [3]

Journal of Neurology

Volumn 249, Issue 5, 2002, Pages 629-630

  Uluc, Kayihan ^a   Arsava, E Murat ^a   Erdem, Sevim ^a   Tan, Ersin ^a  

^a HACETTEPE UNIVERSITY   (Turkey)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ADULT; CASE REPORT; CHROMOSOME 19; CLINICAL FEATURE; DIAGNOSTIC PROCEDURE; FEMALE; HUMAN; LABORATORY TEST; LETTER; MINI MENTAL STATE EXAMINATION; MUSCLE BIOPSY; MUSCLE STRENGTH; MYOPATHY; MYOTONIC DYSTROPHY; NEUROLOGIC EXAMINATION; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; WHITE MATTER;

BRAIN; CHROMOSOMES, HUMAN, PAIR 19; DIAGNOSIS, DIFFERENTIAL; FEMALE; HUMANS; MAGNETIC RESONANCE IMAGING; MIDDLE AGED; MUSCLE WEAKNESS; MUSCLE, SKELETAL; MUTATION; MYOTONIC DISORDERS; MYOTONIC DYSTROPHY; NERVE FIBERS, MYELINATED; PHENOTYPE; TRINUCLEOTIDE REPEAT EXPANSION;

EID: 0036250560     PISSN: 03405354     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004150200076     Document Type: Letter

References (7)

1. Cerebral abnormalities in myotonic dystrophy. Cerebral blood flow, magnetic resonance imaging and neuropsychological tests
2. Proton spectroscopy in myotonic dystrophy: Correlations with CTG repeats
3. Decreased cerebral glucose utilization in myotonic dystrophy
4. Central nervous system magnetic resonance imaging findings in myotonic dystrophy
5. Proximal myotonic myopathy with MRI white matter abnormalities of the brain
6. Clinical and genetic heterogeneity in myotonic dystrophies
7. Anterior temporal white matter lesions in myotonic dystrophy with intellectual impairment: An MRI and neu-ropathological study