Charcot-Marie-Tooth (CMT) disease 1A with superimposed inflammatory polyneuropathy in children

Neuropediatrics

Volumn 40, Issue 2, 2009, Pages 85-88

  Desurkar, A ^a   Lin, J P ^a   Mills, K ^b   Al Sarraj, S ^b   Jan, W ^c   Jungbluth, H ^a,d   Wraige, E ^a  

^a EVELINA LONDON CHILDREN S HOSPITAL   (United Kingdom)

^b KING S COLLEGE HOSPITAL   (United Kingdom)

^c ST THOMAS HOSPITAL   (United Kingdom)

^d KING'S COLLEGE LONDON   (United Kingdom)

Author keywords

acute inflammatory demyelinating polyneuropathy (AIDP); Charcot Marie Tooth (CMT); CMT1A

Indexed keywords

ACUTE INFLAMMATORY DEMYELINATING POLYNEUROPATHY; ARTICLE; CASE REPORT; CHILD; CHROMOSOME 17P; CHRONIC INFLAMMATORY DEMYELINATING POLYNEUROPATHY; CLINICAL FEATURE; ELECTRON MICROSCOPY; FEMALE; GENE; GENE DUPLICATION; HEREDITARY MOTOR SENSORY NEUROPATHY; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; NERVE BIOPSY; NUCLEAR MAGNETIC RESONANCE IMAGING; PMP22 GENE; POLYNEUROPATHY; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD; SURAL NERVE;

CEREBELLUM; CHARCOT-MARIE-TOOTH DISEASE; CHILD; CHILD, PRESCHOOL; DISEASE PROGRESSION; FEMALE; GUILLAIN-BARRE SYNDROME; HUMANS; MAGNETIC RESONANCE IMAGING; MYELIN PROTEINS; SURAL NERVE;

EID: 77954773693     PISSN: 0174304X     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-0029-1237720     Document Type: Article

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