Benign hereditary chorea: An update

Parkinsonism and Related Disorders

Volumn 17, Issue 5, 2011, Pages 301-307

  Inzelberg, Rivka ^a,b   Weinberger, Moran ^b   Gak, Eva ^a,b  

^a SHEBA MEDICAL CENTER   (Israel)

^b TEL AVIV UNIVERSITY   (Israel)

Author keywords

Benign hereditary chorea; Brain thyroid lung syndrome; Chorea; Congenital hypothyroidism; Thyroid transcription factor

Indexed keywords

METHYLPHENIDATE; OLANZAPINE; TETRABENAZINE; THYROID TRANSCRIPTION FACTOR 1;

AUTOSOMAL DISORDER; BENIGN HEREDITARY CHOREA; BRAIN BLOOD FLOW; CHOREA; CLINICAL EVALUATION; CLINICAL FEATURE; COGNITION; CONGENITAL HYPOTHYROIDISM; CONGENITAL LUNG DISEASE; DIFFERENTIAL DIAGNOSIS; DISEASE ASSOCIATION; DISEASE MODEL; GENE FUNCTION; GENE MUTATION; GENETIC ASSOCIATION; GENETIC MARKER; GENOTYPE PHENOTYPE CORRELATION; HUMAN; NEUROIMAGING; NEUROPATHOLOGY; NONHUMAN; PRIORITY JOURNAL; PSYCHOSIS; REVIEW; SYSTEMATIC REVIEW;

ANIMALS; BRAIN; CHOREA; DISEASE MODELS, ANIMAL; DNA-BINDING PROTEINS; HAPLOINSUFFICIENCY; HUMANS; LUNG; MOLECULAR CHAPERONES; NUCLEAR PROTEINS; PHOSPHOPROTEINS; THYROID GLAND; TRANSCRIPTION FACTORS;

EID: 79957953448     PISSN: 13538020     EISSN: 18735126     Source Type: Journal    
DOI: 10.1016/j.parkreldis.2011.01.002     Document Type: Review

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