BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

135 related articles for article (PubMed ID: 20544814)

  • 1. Benign hereditary chorea: clinical and neuroimaging features in an Italian family.
    Salvatore E; Di Maio L; Filla A; Ferrara AM; Rinaldi C; Saccà F; Peluso S; Macchia PE; Pappatà S; De Michele G
    Mov Disord; 2010 Jul; 25(10):1491-6. PubMed ID: 20544814
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 23(12):1744-7. PubMed ID: 18661567
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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; 21(12):2237-40. PubMed ID: 17044090
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 264(1-2):56-62. PubMed ID: 17765926
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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; 22(14):2104-9. PubMed ID: 17702043
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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; 34(3):255-7. PubMed ID: 21555194
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Benign hereditary chorea revisited: a journey to understanding.
    Kleiner-Fisman G; Lang AE
    Mov Disord; 2007 Dec; 22(16):2297-305; quiz 2452. PubMed ID: 17702033
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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; 64(11):1952-4. PubMed ID: 15955952
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutations in TITF1 are not relevant to sporadic and familial chorea of unknown cause.
    Bauer P; Kreuz FR; Bürk K; Saft C; Andrich J; Heilemann H; Riess O; Schöls L
    Mov Disord; 2006 Oct; 21(10):1734-7. PubMed ID: 16830318
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A novel mutation of NKX2-1 affecting 2 generations with hypothyroidism and choreoathetosis: part of the spectrum of brain-thyroid-lung syndrome.
    Williamson S; Kirkpatrick M; Greene S; Goudie D
    J Child Neurol; 2014 May; 29(5):666-9. PubMed ID: 24453141
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Benign hereditary chorea: clinical, neuroimaging, and genetic findings.
    Mahajnah M; Inbar D; Steinmetz A; Heutink P; Breedveld GJ; Straussberg R
    J Child Neurol; 2007 Oct; 22(10):1231-4. PubMed ID: 17940252
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Benign hereditary chorea: dopaminergic brain imaging in patients with a novel intronic NKX2.1 gene mutation.
    Konishi T; Kono S; Fujimoto M; Terada T; Matsushita K; Ouchi Y; Miyajima H
    J Neurol; 2013 Jan; 260(1):207-13. PubMed ID: 22825795
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Alterations of striatal neurons in benign hereditary chorea.
    Kleiner-Fisman G; Calingasan NY; Putt M; Chen J; Beal MF; Lang AE
    Mov Disord; 2005 Oct; 20(10):1353-7. PubMed ID: 15986422
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel NKX2.1 mutation in a family with hypothyroidism and benign hereditary chorea.
    Ferrara AM; De Michele G; Salvatore E; Di Maio L; Zampella E; Capuano S; Del Prete G; Rossi G; Fenzi G; Filla A; Macchia PE
    Thyroid; 2008 Sep; 18(9):1005-9. PubMed ID: 18788921
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A novel de novo mutation of the TITF1/NKX2-1 gene causing ataxia, benign hereditary chorea, hypothyroidism and a pituitary mass in a UK family and review of the literature.
    Veneziano L; Parkinson MH; Mantuano E; Frontali M; Bhatia KP; Giunti P
    Cerebellum; 2014 Oct; 13(5):588-95. PubMed ID: 24930029
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [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; 56(10):515-20. PubMed ID: 23658034
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Benign hereditary chorea.
    Kleiner-Fisman G
    Handb Clin Neurol; 2011; 100():199-212. PubMed ID: 21496579
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Nonsense mutation in TITF1 in a Portuguese family with benign hereditary chorea.
    Costa MC; Costa C; Silva AP; Evangelista P; Santos L; Ferro A; Sequeiros J; Maciel P
    Neurogenetics; 2005 Dec; 6(4):209-15. PubMed ID: 16220345
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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; 83(10):956-62. PubMed ID: 22832740
    [TBL] [Abstract][Full Text] [Related]  

  • 20. NKX2-1 mutations in brain-lung-thyroid syndrome: a case series of four patients.
    Shetty VB; Kiraly-Borri C; Lamont P; Bikker H; Choong CS
    J Pediatr Endocrinol Metab; 2014 Mar; 27(3-4):373-8. PubMed ID: 24129101
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.