These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
137 related articles for article (PubMed ID: 25412988)
1. 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; 57(8):777-9. PubMed ID: 25412988 [TBL] [Abstract][Full Text] [Related]
2. l-Thyroxine-responsive drop attacks in childhood benign hereditary chorea: A case report. Shiohama T; Ohashi H; Shimizu K; Fujii K; Oba D; Takatani T; Kato M; Shimojo N Brain Dev; 2018 Apr; 40(4):353-356. PubMed ID: 29289388 [TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. 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]
6. 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]
7. 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]
8. 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]
9. Growth hormone deficiency in a child with benign hereditary chorea caused by a Trevisani V; Predieri B; Madeo SF; Fusco C; Garavelli L; Caraffi S; Iughetti L J Pediatr Endocrinol Metab; 2022 Mar; 35(3):411-415. PubMed ID: 34710315 [TBL] [Abstract][Full Text] [Related]
10. 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; 23(2):91-102. PubMed ID: 35079915 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. [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]
14. 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]
15. 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]
16. Five new TTF1/NKX2.1 mutations in brain-lung-thyroid syndrome: rescue by PAX8 synergism in one case. Carré A; Szinnai G; Castanet M; Sura-Trueba S; Tron E; Broutin-L'Hermite I; Barat P; Goizet C; Lacombe D; Moutard ML; Raybaud C; Raynaud-Ravni C; Romana S; Ythier H; Léger J; Polak M Hum Mol Genet; 2009 Jun; 18(12):2266-76. PubMed ID: 19336474 [TBL] [Abstract][Full Text] [Related]
17. Multiplex Ligation-dependent Probe Amplification improves the detection rate of NKX2.1 mutations in patients affected by brain-lung-thyroid syndrome. Teissier R; Guillot L; Carré A; Morandini M; Stuckens C; Ythier H; Munnich A; Szinnai G; de Blic J; Clement A; Leger J; Castanet M; Epaud R; Polak M Horm Res Paediatr; 2012; 77(3):146-51. PubMed ID: 22488412 [TBL] [Abstract][Full Text] [Related]
18. Benign hereditary chorea related to NKX2.1: expansion of the genotypic and phenotypic spectrum. Peall KJ; Lumsden D; Kneen R; Madhu R; Peake D; Gibbon F; Lewis H; Hedderly T; Meyer E; Robb SA; Lynch B; King MD; Lin JP; Morris HR; Jungbluth H; Kurian MA Dev Med Child Neurol; 2014 Jul; 56(7):642-8. PubMed ID: 24171694 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. [Description of an endogamous, multigenerational and extensive family with benign hereditary chorea from the Paisa community]. Pérez-Póveda JC; Palacio LG; Arcos-Burgos M Rev Neurol; 2005 Jul 16-31; 41(2):95-8. PubMed ID: 16028188 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]