217 related articles for article (PubMed ID: 15955952)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. "Jerky" dystonia in children: spectrum of phenotypes and genetic testing.
Asmus F; Langseth A; Doherty E; Nestor T; Munz M; Gasser T; Lynch T; King MD
Mov Disord; 2009 Apr; 24(5):702-9. PubMed ID: 19117362
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. 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]
11. 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]
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]
13. 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]
14. Choreoathetosis, hypothyroidism, and pulmonary alterations due to human NKX2-1 haploinsufficiency.
Krude H; Schütz B; Biebermann H; von Moers A; Schnabel D; Neitzel H; Tönnies H; Weise D; Lafferty A; Schwarz S; DeFelice M; von Deimling A; van Landeghem F; DiLauro R; Grüters A
J Clin Invest; 2002 Feb; 109(4):475-80. PubMed ID: 11854319
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. 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]
18. 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]
19. 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]
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]
