Nerve root hypertrophy in CMT type 1A

Neurology

Volumn 62, Issue 5, 2004, Pages 783-

  Liao, Jenny P ^a   Waclawik, Andrew J ^a,b  

^a UW Medical School ^*

^b UNIVERSITY OF WISCONSIN SCHOOL OF MEDICINE AND PUBLIC HEALTH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CASE REPORT; DEMYELINATION; DNA DETERMINATION; FOOT MALFORMATION; GENE; GENE DUPLICATION; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; HYPERTROPHY; MALE; NERVE CONDUCTION; NERVE ROOT; NEUROFIBROMATOSIS; NUCLEAR MAGNETIC RESONANCE IMAGING; PMP22 GENE; PRIORITY JOURNAL; SCOLIOSIS;

EID: 1542316170     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/01.WNL.0000103234.32489.CA     Document Type: Article

References (2)

1. Martinoli C, Schenone A, Bianchi S, et al. Sonography of the median nerve in Charcot-Marie-Tooth disease. AJR Am J Radiol 2002;178:1553-1556.
2. Midroni G, Noel de Tilly L, Gray B, et al. MRI of the cauda equina in CIDP: clinical correlations. J Neurol Sci 1999;170:36-44.