126 related articles for article (PubMed ID: 7960679)
1. Spasmodic dystonic laterocollis in familial cerebellar ataxia.
Carella F; Ciano C; Pandolfo M; Giovannini P; Girotti F; Caraceni T
Ital J Neurol Sci; 1994 Jun; 15(5):245-8. PubMed ID: 7960679
[TBL] [Abstract][Full Text] [Related]
2. Slowly progressive cerebellar ataxia and cervical dystonia: clinical presentation of a new form of spinocerebellar ataxia?
Kuoppamäki M; Giunti P; Quinn N; Wood NW; Bhatia KP
Mov Disord; 2003 Feb; 18(2):200-6. PubMed ID: 12539216
[TBL] [Abstract][Full Text] [Related]
3. Denervation and myotomy of muscles of the omotrapezoid triangle of the neck improve the outcomes of surgical treatment of laterocollis and torticollis subtypes of spasmodic torticollis: 58 case analysis.
Tsymbaliuk VI; Tretyak IB; Freidman MY; Gatskiy AA
Acta Neurochir (Wien); 2016 Jun; 158(6):1159-64. PubMed ID: 27052514
[TBL] [Abstract][Full Text] [Related]
4. Novel CACNA1A variant may cause cervical dystonia and cerebellar ataxia syndrome.
Fuerte-Hortigón A; Pérez-Noguera R; Dotor García-Soto J; Royo Boronat I; Álvarez de Andrés S; García-Moreno JM
J Neurol Sci; 2020 Aug; 415():116909. PubMed ID: 32480075
[No Abstract] [Full Text] [Related]
5. Subclinical celiac disease with cerebellar ataxia.
Tunc T; Okuyucu E; Ucleri S; Sonmez T; Coskun O; Selvi E; Inan LE
Acta Neurol Belg; 2004 Jun; 104(2):84-6. PubMed ID: 15508272
[TBL] [Abstract][Full Text] [Related]
6. Migraine associated with focal cerebral edema, cerebrospinal fluid pleocytosis, and progressive cerebellar ataxia: MRI documentation.
Goldstein JM; Shaywitz BA; Sze G; Nallainathan S
Neurology; 1990 Aug; 40(8):1284-7. PubMed ID: 2381540
[No Abstract] [Full Text] [Related]
7. Congenital cerebellar ataxia, mental retardation, and atrophic retinal lesions in two brothers.
Ferri R; Azan G; Del Gracco S; Elia M; Musumeci SA; Stefanini MC; Toscano G; Setta F
J Neurol Neurosurg Psychiatry; 1996 Oct; 61(4):424-5. PubMed ID: 8890793
[No Abstract] [Full Text] [Related]
8. Magnetic resonance imaging in familial paroxysmal ataxia.
Vighetto A; Froment JC; Trillet M; Aimard G
Arch Neurol; 1988 May; 45(5):547-9. PubMed ID: 3358708
[TBL] [Abstract][Full Text] [Related]
9. Case 20-2021: A 69-Year-Old Man with Ataxia.
Khurana V; de Gusmao CM; Glover M; Helgager J
N Engl J Med; 2021 Jul; 385(2):165-175. PubMed ID: 34233100
[No Abstract] [Full Text] [Related]
10. An autopsy confirmed case of progressive supranuclear palsy with predominant cerebellar ataxia.
Lee MJ; Lee JH; Kim BK; Lee JH; Lee YM; Kim SJ; Shin JH; Shin MJ; Ahn JW; Sung S; Choi KU; Jung DS; Jung NY; Seeley WW; Huh GY; Kim EJ
J Neurol; 2016 Dec; 263(12):2540-2543. PubMed ID: 27761640
[No Abstract] [Full Text] [Related]
11. Congenital disorder of glycosylation type Ia presenting as early-onset cerebellar ataxia in an adult.
Schoffer KL; O'Sullivan JD; McGill J
Mov Disord; 2006 Jun; 21(6):869-72. PubMed ID: 16482534
[TBL] [Abstract][Full Text] [Related]
12. Hypergonadotropic hypogonadism and cerebellar ataxia: an unusual association.
Braga-Neto P; Martins MC; Santos-Neto D; Weisman P; Costa Ede P; Pinto LM; Santos-Galduroz RF; Verreschi IT; Barsottini OG
Arq Neuropsiquiatr; 2010 Feb; 68(1):132-4. PubMed ID: 20339668
[No Abstract] [Full Text] [Related]
13. Hereditary cerebellar ataxia with Leber's hereditary optic neuropathy mitochondrial DNA 11778 mutation.
Murakami T; Mita S; Tokunaga M; Maeda H; Ueyama H; Kumamoto T; Uchino M; Ando M
J Neurol Sci; 1996 Oct; 142(1-2):111-3. PubMed ID: 8902729
[TBL] [Abstract][Full Text] [Related]
14. A serial MRI study in a patient with progressive supranuclear palsy with cerebellar ataxia.
Kanazawa M; Shimohata T; Endo K; Koike R; Takahashi H; Nishizawa M
Parkinsonism Relat Disord; 2012 Jun; 18(5):677-9. PubMed ID: 22153384
[No Abstract] [Full Text] [Related]
15. Comparison of 2 Operative Methods for Treating Laterocollis and Torticollis Subtypes of Spasmodic Torticollis: Follow-Up of 121 Cases.
Li X; Li S; Pu B; Hua C
World Neurosurg; 2017 Dec; 108():636-641. PubMed ID: 28939542
[TBL] [Abstract][Full Text] [Related]
16. Maternally inherited diabetes and deafness with cerebellar ataxia: a new clinical phenotype associated with the mitochondrial DNA 3243 mutation.
Arai M; Ohshima S
J Neurol; 1997 Jul; 244(7):468-9. PubMed ID: 9266470
[No Abstract] [Full Text] [Related]
17. Spastic paraparesis, cerebellar ataxia, and intention tremor: a severe variant of FXTAS?
Jacquemont S; Orrico A; Galli L; Sahota PK; Brunberg JA; Anichini C; Leehey M; Schaeffer S; Hagerman RJ; Hagerman PJ; Tassone F
J Med Genet; 2005 Feb; 42(2):e14. PubMed ID: 15689437
[No Abstract] [Full Text] [Related]
18. [Peripheral neuropathies associated with hereditary cerebellar ataxias].
Anheim M; Tranchant C
Rev Neurol (Paris); 2011 Jan; 167(1):72-6. PubMed ID: 21195440
[TBL] [Abstract][Full Text] [Related]
19. Familial cerebellar ataxia presenting with down beat nystagmus.
Schott GD
J Med Genet; 1980 Apr; 17(2):115-8. PubMed ID: 7381864
[TBL] [Abstract][Full Text] [Related]
20. Familial cosegregation of manic-depressive illness and a form of hereditary cerebellar ataxia.
Fernández Piqueras J; Santos J; Visedo G; Pérez de Castro I; Puertollano R; Montejo J; Ramo Tello C; Valle J
Am J Med Genet; 1995 Jun; 60(3):206-9. PubMed ID: 7573172
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]