233 related articles for article (PubMed ID: 16028188)
21. Hereditary chorea without dementia.
Behan PO; Bone I
J Neurol Neurosurg Psychiatry; 1977 Jul; 40(7):687-91. PubMed ID: 144176
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. 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]
24. [Linkage analysis of the 15q25-15q22 region in an extended multigenerational family segregating for idiopathic epilepsy].
Palacio LG; Sánchez JL; Jiménez ME; Rivera-Valencia D; Jiménez-Ramírez I; Arcos-Burgos M
Rev Neurol; 2004 Dec 1-15; 39(11):1021-5. PubMed ID: 15597263
[TBL] [Abstract][Full Text] [Related]
25. Chorea-acanthocytosis: a report of three new families and implications for genetic counselling.
Vance JM; Pericak-Vance MA; Bowman MH; Payne CS; Fredane L; Siddique T; Roses AD; Massey EW
Am J Med Genet; 1987 Oct; 28(2):403-10. PubMed ID: 3322006
[TBL] [Abstract][Full Text] [Related]
26. 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]
27. [Epidemiology and cases of early manifestations of Huntington chorea].
Khannanova FK
Zh Nevropatol Psikhiatr Im S S Korsakova; 1987; 87(3):340-2. PubMed ID: 2953156
[TBL] [Abstract][Full Text] [Related]
28. [Chronic non-progressive form of chorea].
Bakhur VT; Chekler LA; Starodubtseva GK
Zh Nevropatol Psikhiatr Im S S Korsakova; 1987; 87(3):353-5. PubMed ID: 2953157
[TBL] [Abstract][Full Text] [Related]
29. [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]
30. [Benign familial chorea: report of 2 cases].
Barbosa ER; De Navarro JM; Diament AJ
Arq Neuropsiquiatr; 1985 Jun; 43(2):180-6. PubMed ID: 4062603
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. Familial essential ("benign") chorea.
Bird TD; Carlson CB; Hall JG
J Med Genet; 1976 Oct; 13(5):357-62. PubMed ID: 1003446
[TBL] [Abstract][Full Text] [Related]
33. Huntington disease: a case study of early onset presenting as depression.
Duesterhus P; Schimmelmann BG; Wittkugel O; Schulte-Markwort M
J Am Acad Child Adolesc Psychiatry; 2004 Oct; 43(10):1293-7. PubMed ID: 15381897
[TBL] [Abstract][Full Text] [Related]
34. [Benign, hereditary, non-progressive chorea--an important differential diagnosis (author's transl)].
Foerster K; Foerster G
Nervenarzt; 1978 Dec; 49(12):724-5. PubMed ID: 153479
[No Abstract] [Full Text] [Related]
35. 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]
36. Clinical and genetic heterogeneity in benign hereditary chorea.
Breedveld GJ; Percy AK; MacDonald ME; de Vries BB; Yapijakis C; Dure LS; Ippel EF; Sandkuijl LA; Heutink P; Arts WF
Neurology; 2002 Aug; 59(4):579-84. PubMed ID: 12196653
[TBL] [Abstract][Full Text] [Related]
37. Chorea-acanthocytosis: a mimicker of Huntington disease case report and review of the literature.
Gold MM; Shifteh K; Bello JA; Lipton M; Kaufman DM; Brown AD
Neurologist; 2006 Nov; 12(6):327-9. PubMed ID: 17122731
[TBL] [Abstract][Full Text] [Related]
38. [Gene diagnosis of patients with chorea].
Shimohata T; Onodera O; Honma Y; Hirota K; Nunomura Y; Kimura T; Kawachi I; Sanpei K; Nishizawa M; Tsuji S
Rinsho Shinkeigaku; 2004 Mar; 44(3):149-53. PubMed ID: 15233265
[TBL] [Abstract][Full Text] [Related]
39. Benign hereditary chorea.
Kleiner-Fisman G
Handb Clin Neurol; 2011; 100():199-212. PubMed ID: 21496579
[TBL] [Abstract][Full Text] [Related]
40. The differential diagnosis of chorea.
Wild EJ; Tabrizi SJ
Pract Neurol; 2007 Nov; 7(6):360-73. PubMed ID: 18024776
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
