Cognitive profile in childhood myotonic dystrophy type 1: Is there a global impairment?

Neuromuscular Disorders

Volumn 17, Issue 6, 2007, Pages 451-458

  Angeard, Nathalie ^a   Gargiulo, Marcela ^a   Jacquette, Aurélia ^a   Radvanyi, Hélène ^b   Eymard, Bruno ^a   Héron, Delphine ^a  

^a PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^b HÔPITAL AMBROISE PARÉ   (France)

Author keywords

(CTG)n; Childhood onset form; Cognitive impairment; Myotonic dystrophy; Transmitting parent's sex

Indexed keywords

ADULT; ARTICLE; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; COGNITIVE DEFECT; CONTROLLED STUDY; DEPTH PERCEPTION; DISEASE COURSE; FEMALE; HUMAN; INTELLIGENCE QUOTIENT; MALE; MEMORY; MYOTONIC DYSTROPHY; PRIORITY JOURNAL; STATISTICAL SIGNIFICANCE;

ADOLESCENT; AGE OF ONSET; CHILD; COGNITION; COGNITION DISORDERS; FEMALE; GENES, X-LINKED; GENES, Y-LINKED; HUMANS; INTELLIGENCE; LEARNING DISORDERS; MALE; MYOTONIC DYSTROPHY; PROTEIN-SERINE-THREONINE KINASES; TRINUCLEOTIDE REPEAT EXPANSION; TRINUCLEOTIDE REPEATS;

EID: 34249018562     PISSN: 09608966     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.nmd.2007.02.012     Document Type: Article

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