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.
138 related articles for article (PubMed ID: 34710315)
1. 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]
2. 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]
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; 83(10):956-62. PubMed ID: 22832740 [TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. 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]
8. 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]
9. A Case of Chorea with Slow Saccades Caused by NKX2-1 Mutation. Vercammen J; Terryn J; Van Daele S; Vermeer S; Vandenberghe W Mov Disord Clin Pract; 2024 Jun; 11(6):738-741. PubMed ID: 38454250 [No Abstract] [Full Text] [Related]
10. 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]
11. A further case of brain-lung-thyroid syndrome with deletion proximal to NKX2-1. Kharbanda M; Hermanns P; Jones J; Pohlenz J; Horrocks I; Donaldson M Eur J Med Genet; 2017 May; 60(5):257-260. PubMed ID: 28286255 [TBL] [Abstract][Full Text] [Related]
12. Mutations in TITF-1 are associated with benign hereditary chorea. Breedveld GJ; van Dongen JW; Danesino C; Guala A; Percy AK; Dure LS; Harper P; Lazarou LP; van der Linde H; Joosse M; Grüters A; MacDonald ME; de Vries BB; Arts WF; Oostra BA; Krude H; Heutink P Hum Mol Genet; 2002 Apr; 11(8):971-9. PubMed ID: 11971878 [TBL] [Abstract][Full Text] [Related]
13. A novel nonsense mutation in the TITF-1 gene in a Japanese family with benign hereditary chorea. Nakamura K; Sekijima Y; Nagamatsu K; Yoshida K; Ikeda S J Neurol Sci; 2012 Feb; 313(1-2):189-92. PubMed ID: 21982616 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. [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]
16. 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]
17. Choreoathetosis, congenital hypothyroidism and neonatal respiratory distress syndrome with intact NKX2-1. Barnett CP; Mencel JJ; Gecz J; Waters W; Kirwin SM; Vinette KM; Uppill M; Nicholl J Am J Med Genet A; 2012 Dec; 158A(12):3168-73. PubMed ID: 23169673 [TBL] [Abstract][Full Text] [Related]
18. Benign hereditary chorea: an update. Inzelberg R; Weinberger M; Gak E Parkinsonism Relat Disord; 2011 Jun; 17(5):301-7. PubMed ID: 21292530 [TBL] [Abstract][Full Text] [Related]
19. Benign hereditary chorea and deletions outside NKX2-1: What's the role of MBIP? Invernizzi F; Zorzi G; Legati A; Coppola G; D'Adamo P; Nardocci N; Garavaglia B; Ghezzi D Eur J Med Genet; 2018 Oct; 61(10):581-584. PubMed ID: 29621620 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]