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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

221 related items for PubMed ID: 16830318

  • 1.
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  • 2. Psychosis, short stature in benign hereditary chorea: a novel thyroid transcription factor-1 mutation.
    Glik A, Vuillaume I, Devos D, Inzelberg R.
    Mov Disord; 2008 Sep 15; 23(12):1744-7. PubMed ID: 18661567
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  • 3. 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.
    Gras D, Jonard L, Roze E, Chantot-Bastaraud S, Koht J, Motte J, Rodriguez D, Louha M, Caubel I, Kemlin I, Lion-François L, Goizet C, Guillot L, Moutard ML, Epaud R, Héron B, Charles P, Tallot M, Camuzat A, Durr A, Polak M, Devos D, Sanlaville D, Vuillaume I, Billette de Villemeur T, Vidailhet M, Doummar D.
    J Neurol Neurosurg Psychiatry; 2012 Oct 15; 83(10):956-62. PubMed ID: 22832740
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  • 4. Functional characterization of a novel mutation in TITF-1 in a patient with benign hereditary chorea.
    Provenzano C, Veneziano L, Appleton R, Frontali M, Civitareale D.
    J Neurol Sci; 2008 Jan 15; 264(1-2):56-62. PubMed ID: 17765926
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  • 5. TITF-1 gene mutation in a case of sporadic non-progressive chorea. Response to levodopa treatment.
    Fons C, Rizzu P, Garcia-Cazorla A, Martorell L, Ormazabal A, Artuch R, Campistol J, Fernandez-Alvarez E.
    Brain Dev; 2012 Mar 15; 34(3):255-7. PubMed ID: 21555194
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  • 7. Clinical differentiation of genetically proven benign hereditary chorea and myoclonus-dystonia.
    Asmus F, Devlin A, Munz M, Zimprich A, Gasser T, Chinnery PF.
    Mov Disord; 2007 Oct 31; 22(14):2104-9. PubMed ID: 17702043
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  • 13. New syndromic form of benign hereditary chorea is associated with a deletion of TITF-1 and PAX-9 contiguous genes.
    Devos D, Vuillaume I, de Becdelievre A, de Martinville B, Dhaenens CM, Cuvellier JC, Cuisset JM, Vallée L, Lemaitre MP, Bourteel H, Hachulla E, Wallaert B, Destée A, Defebvre L, Sablonnière B.
    Mov Disord; 2006 Dec 31; 21(12):2237-40. PubMed ID: 17044090
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  • 14. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug 31; 56(3):105-52. PubMed ID: 19728970
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  • 15. Microdeletions detected using chromosome microarray in children with suspected genetic movement disorders: a single-centre study.
    Dale RC, Grattan-Smith P, Nicholson M, Peters GB.
    Dev Med Child Neurol; 2012 Jul 31; 54(7):618-23. PubMed ID: 22515636
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  • 16. Benign hereditary chorea.
    Kleiner-Fisman G.
    Handb Clin Neurol; 2011 Jul 31; 100():199-212. PubMed ID: 21496579
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  • 17. [Chorea due to TITF1/NKX2-1 mutation: phenotypical description and therapeutic response in a family].
    Salvado M, Boronat-Guerrero S, Hernández-Vara J, Álvarez-Sabin J.
    Rev Neurol; 2013 May 16; 56(10):515-20. PubMed ID: 23658034
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  • 18. A novel TITF-1 mutation causes benign hereditary chorea with response to levodopa.
    Asmus F, Horber V, Pohlenz J, Schwabe D, Zimprich A, Munz M, Schöning M, Gasser T.
    Neurology; 2005 Jun 14; 64(11):1952-4. PubMed ID: 15955952
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  • 19. Recurrent drop attacks in early childhood as presenting symptom of benign hereditary chorea caused by TITF1 gene mutations.
    Rosati A, Berti B, Melani F, Cellini E, Procopio E, Guerrini R.
    Dev Med Child Neurol; 2015 Aug 14; 57(8):777-9. PubMed ID: 25412988
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  • 20. Altered pituitary morphology as a sign of benign hereditary chorea caused by TITF1/NKX2.1 mutations.
    Thust S, Veneziano L, Parkinson MH, Bhatia KP, Mantuano E, Gonzalez-Robles C, Davagnanam I, Giunti P.
    Neurogenetics; 2022 Apr 14; 23(2):91-102. PubMed ID: 35079915
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