Atypical hereditary spastic paraplegia mimicking multiple sclerosis associated with a novel SPG11 mutation

European Journal of Neurology

Volumn 21, Issue 2, 2014, Pages

  Romagnolo, A ^a   Masera, S ^a   Mattioda, A ^a   Superti, G ^a   Santorelli, F M ^b   Mongini, T ^a   Pinessi, L ^a   Cavalla, P ^a  

^a UNIVERSITY OF TURIN   (Italy)

^b DEPARTMENT OF DEVELOPMENTAL NEUROSCIENCE   (Italy)

Author keywords

Corpus callosum; Hereditary spastic paraplegia; Magnetic resonance imaging; Multiple sclerosis; White matter abnormalities

Indexed keywords

GADOLINIUM;

ACHILLES REFLEX; ADULT; ATTENTION DISTURBANCE; BRAIN ATROPHY; CASE REPORT; CLINICAL EVALUATION; CONTRAST ENHANCEMENT; CORPUS CALLOSUM; DISEASE COURSE; DISEASE EXACERBATION; DNA DETERMINATION; DYSARTHRIA; EVOKED MUSCLE RESPONSE; EVOKED SOMATOSENSORY RESPONSE; FACIAL NERVE PARALYSIS; FEMALE; FOLLOW UP; GAIT DISORDER; GENE; GENE MUTATION; GENETIC VARIABILITY; HEMIPARESIS; HEREDITARY MOTOR SENSORY NEUROPATHY; HETEROZYGOSITY; HUMAN; LEARNING DISORDER; LETTER; LEUKOENCEPHALOPATHY; MEMORY DISORDER; MINI MENTAL STATE EXAMINATION; MULTIPLE SCLEROSIS; MUSCLE CRAMP; NERVE FIBER TRANSPORT; NEUROIMAGING; NEUROLOGIC EXAMINATION; NEUROPSYCHOLOGICAL TEST; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; PSYCHOMOTOR DEVELOPMENT; PYRAMIDAL SIGN; SPG11 GENE; URGE INCONTINENCE; VERBAL COMMUNICATION; VIBRATION SENSE; WEAKNESS; WHITE MATTER LESION;

CORPUS CALLOSUM; HEREDITARY SPASTIC PARAPLEGIA; MAGNETIC RESONANCE IMAGING; MULTIPLE SCLEROSIS; WHITE MATTER ABNORMALITIES;

BRAIN; DIAGNOSIS, DIFFERENTIAL; FEMALE; HUMANS; MAGNETIC RESONANCE IMAGING; MULTIPLE SCLEROSIS; NERVE FIBERS, MYELINATED; PROTEINS; SPASTIC PARAPLEGIA, HEREDITARY; YOUNG ADULT;

EID: 84892459293     PISSN: 13515101     EISSN: 14681331     Source Type: Journal    
DOI: 10.1111/ene.12297     Document Type: Letter

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