Metachromatic leukodystrophy and nonverbal learning disability: Neuropsychological and neuroradiological findings in heterozygous carriers

Child Neuropsychology

Volumn 7, Issue 1, 2001, Pages 54-58

  Weber Byars, Anna M ^a   McKellop, J Mark ^a   Gyato, Kunsang ^a   Sullivan, Tom ^a   Franz, David N ^a  

^a CINCINNATI CHILDREN'S HOSPITAL MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CEREBROSIDE SULFATASE;

ADULT; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; DEGENERATIVE DISEASE; DEMYELINATION; ENZYME DEFICIENCY; FAMILY; FEMALE; GENE MUTATION; HETEROZYGOTE; HUMAN; LEARNING DISORDER; MALE; METACHROMATIC LEUKODYSTROPHY; NEUROPSYCHOLOGICAL TEST; NONVERBAL COMMUNICATION; NUCLEAR MAGNETIC RESONANCE IMAGING; WHITE MATTER;

ADOLESCENT; ADULT; BRAIN; CEREBROSIDE-SULFATASE; CHILD; CHILD, PRESCHOOL; FAMILY; FEMALE; GENOTYPE; HETEROZYGOTE; HUMANS; LEARNING DISORDERS; LEUKODYSTROPHY, METACHROMATIC; MAGNETIC RESONANCE IMAGING; MALE; NEUROPSYCHOLOGICAL TESTS; PHENOTYPE; SYNDROME;

EID: 0035705736     PISSN: 09297049     EISSN: None     Source Type: Journal    
DOI: 10.1076/chin.7.1.54.3146     Document Type: Article

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