Benign hereditary chorea: Phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the TITF1/NKX2-1 gene

Journal of Neurology, Neurosurgery and Psychiatry

Volumn 83, Issue 10, 2012, Pages 956-962

  Gras, Domitille ^a   Jonard, Laurence ^a   Roze, Emmanuel ^b,c,d   Chantot Bastaraud, Sandra ^b   Koht, Jeanette ^e   Motte, Jacques ^f   Rodriguez, Diana ^a,d,g   Louha, Malek ^a   Caubel, Isabelle ^h   Kemlin, Isabelle ^a   Lion François, Laurence ⁱ   Goizet, Cyril ^j   Guillot, Loic ^k   Moutard, Marie Laure ^a,g   Epaud, Ralph ^l   Héron, Bénédicte ^a,g   Charles, Perrine ^g,m   Tallot, Marilyn ^a,d   Camuzat, Agnès ^c,m   Durr, Alexandra ^c,d,g,m   Polak, Michel ^b   Devos, David ⁿ   Sanlaville, Damien ^o,p   Vuillaume, Isabelle ^q   De Villemeur, Thierry Billette ^a,d,g   Vidailhet, Marie ^b,c,d,g   Doummar, Diane ^a,g   more..

^a ARMAND TROUSSEAU HOSPITAL   (France)

^b ASSISTANCE PUBLIQUE HÔPITAUX DE PARIS   (France)

^c INSTITUT DU CERVEAU ET DE LA MOELLE ÉPINIÈRE   (France)

^d SORBONNE UNIVERSITÉ   (France)

^e OSLO UNIVERSITY HOSPITAL   (Norway)

^f AMERICAN MEMORIAL HOSPITAL   (France)

^g hôpitaux universitaires de l'Est Parisien   (France)

^h HÔPITAL ARMAND TROUSSEAU   (France)

ⁱ UNIVERSITÉ DE LYON   (France)

^j BORDEAUX UNIVERSITY HOSPITAL   (France)

^k UNIVERSITÉ PARIS DESCARTES   (France)

^l CENTRE HOSPITALIER INTERCOMMUNAL DE CRÉTEIL   (France)

^m PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

ⁿ UNIV LILLE   (France)

^o HOSPICES CIVILS DE LYON   (France)

^p UNIVERSITÉ LYON 1   (France)

^q LILLE UNIVERSITY HOSPITAL   (France)

more..

Author keywords

[No Author keywords available]

Indexed keywords

FLUTICASONE; LEVODOPA; TETRABENAZINE;

ADULT; ASTHENIA; ASTHMA; ATTENTION DEFICIT DISORDER; BENIGN HEREDITARY CHOREA; CHILD; CHOREA; CHROMOSOME 14Q; CLINICAL ARTICLE; COMPARATIVE GENOMIC HYBRIDIZATION; CONGENITAL HYPOTHYROIDISM; DISEASE COURSE; DISEASE SEVERITY; DNA SEQUENCE; DRUG DOSE INCREASE; DRUG EFFICACY; DRUG TOLERABILITY; DRUG WITHDRAWAL; DYSTONIA; FEMALE; FOLLOW UP; GAIT DISORDER; GENE; GENE MUTATION; HUMAN; HYPOTHYROIDISM; INTERSTITIAL CHROMOSOME DELETION; LEARNING DISORDER; MALE; MENTAL DEFICIENCY; MUSCLE HYPOTONIA; MUTATIONAL ANALYSIS; MYOCLONUS; NKX2-1 GENE; NUCLEOTIDE SEQUENCE; PAX9 GENE; PRESCHOOL CHILD; PRIORITY JOURNAL; PROGNOSIS; RECURRENT INFECTION; RESPIRATORY FAILURE; RESPIRATORY TRACT DISEASE; REVIEW; SPEECH DISORDER; THYROID DISEASE; TIC;

ADRENERGIC UPTAKE INHIBITORS; ADULT; AGE OF ONSET; ATTENTION DEFICIT DISORDER WITH HYPERACTIVITY; CHILD; CHILD, PRESCHOOL; CHOREA; CHROMOSOME DISORDERS; COGNITION DISORDERS; CONGENITAL HYPOTHYROIDISM; DNA MUTATIONAL ANALYSIS; FEMALE; FOLLOW-UP STUDIES; FRANCE; GENES, DOMINANT; HUMANS; INFANT; MALE; MUTATION; NEUROPSYCHOLOGICAL TESTS; NUCLEAR PROTEINS; PHENOTYPE; PROGNOSIS; PROTEIN ARRAY ANALYSIS; RESPIRATORY TRACT DISEASES; TETRABENAZINE; TRANSCRIPTION FACTORS; TREATMENT OUTCOME;

EID: 84866149000     PISSN: 00223050     EISSN: 1468330X     Source Type: Journal    
DOI: 10.1136/jnnp-2012-302505     Document Type: Review

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