129 related articles for article (PubMed ID: 21243258)
41. Causes of progressive cerebellar ataxia: prospective evaluation of 1500 patients.
Hadjivassiliou M; Martindale J; Shanmugarajah P; Grünewald RA; Sarrigiannis PG; Beauchamp N; Garrard K; Warburton R; Sanders DS; Friend D; Duty S; Taylor J; Hoggard N
J Neurol Neurosurg Psychiatry; 2017 Apr; 88(4):301-309. PubMed ID: 27965395
[TBL] [Abstract][Full Text] [Related]
42. Ataxia with oculomotor apraxia type 2: a clinical and genetic study of 19 patients.
Tazir M; Ali-Pacha L; M'Zahem A; Delaunoy JP; Fritsch M; Nouioua S; Benhassine T; Assami S; Grid D; Vallat JM; Hamri A; Koenig M
J Neurol Sci; 2009 Mar; 278(1-2):77-81. PubMed ID: 19141356
[TBL] [Abstract][Full Text] [Related]
43. Ultrastructural sperm abnormalities and cerebellar atrophy: does a correlation exist? Report of two cases without endocrine hypogonadism.
Malandrini A; Villanova M; Piomboni P; Collodel G; Spadaro M; Giunti P; Salvadori C; Morocutti C; Guazzi GC
J Submicrosc Cytol Pathol; 1993 Jul; 25(3):371-5. PubMed ID: 8402537
[TBL] [Abstract][Full Text] [Related]
44. Paroxysmal cerebellar ataxia.
Goadsby PJ; Boyce G
Aust N Z J Med; 1990 Feb; 20(1):103. PubMed ID: 2322195
[No Abstract] [Full Text] [Related]
45. Molecular and clinical study of a cohort of 110 Algerian patients with autosomal recessive ataxia.
Hamza W; Ali Pacha L; Hamadouche T; Muller J; Drouot N; Ferrat F; Makri S; Chaouch M; Tazir M; Koenig M; Benhassine T
BMC Med Genet; 2015 Jun; 16():36. PubMed ID: 26068213
[TBL] [Abstract][Full Text] [Related]
46. Comparing ataxias with oculomotor apraxia: a multimodal study of AOA1, AOA2 and AT focusing on video-oculography and alpha-fetoprotein.
Mariani LL; Rivaud-Péchoux S; Charles P; Ewenczyk C; Meneret A; Monga BB; Fleury MC; Hainque E; Maisonobe T; Degos B; Echaniz-Laguna A; Renaud M; Wirth T; Grabli D; Brice A; Vidailhet M; Stoppa-Lyonnet D; Dubois-d'Enghien C; Le Ber I; Koenig M; Roze E; Tranchant C; Durr A; Gaymard B; Anheim M
Sci Rep; 2017 Nov; 7(1):15284. PubMed ID: 29127364
[TBL] [Abstract][Full Text] [Related]
47. [Chronic ataxia in childhood].
Erazo Torricelli R
Medicina (B Aires); 2013; 73 Suppl 1():38-48. PubMed ID: 24072050
[TBL] [Abstract][Full Text] [Related]
48. Classification of the hereditary ataxias and paraplegias.
Harding AE
Lancet; 1983 May; 1(8334):1151-5. PubMed ID: 6133167
[No Abstract] [Full Text] [Related]
49. [Mutations in SYNE-1 lead to a newly discovered form of autosomal recessive cerebellar ataxia].
Dupré N; Bouchard JP; Gros-Louis F; Rouleau GA
Med Sci (Paris); 2007 Mar; 23(3):261-2. PubMed ID: 17349286
[No Abstract] [Full Text] [Related]
50. Genetic cerebellar ataxias.
Storey E
Semin Neurol; 2014 Jul; 34(3):280-92. PubMed ID: 25192506
[TBL] [Abstract][Full Text] [Related]
51. A panel study on patients with dominant cerebellar ataxia highlights the frequency of channelopathies.
Coutelier M; Coarelli G; Monin ML; Konop J; Davoine CS; Tesson C; Valter R; Anheim M; Behin A; Castelnovo G; Charles P; David A; Ewenczyk C; Fradin M; Goizet C; Hannequin D; Labauge P; Riant F; Sarda P; Sznajer Y; Tison F; Ullmann U; Van Maldergem L; Mochel F; Brice A; Stevanin G; Durr A;
Brain; 2017 Jun; 140(6):1579-1594. PubMed ID: 28444220
[TBL] [Abstract][Full Text] [Related]
52. Autosomal-recessive cerebellar ataxias.
Fogel BL
Handb Clin Neurol; 2018; 147():187-209. PubMed ID: 29325611
[TBL] [Abstract][Full Text] [Related]
53. Autosomal Recessive Cerebellar Ataxias in Europe: Frequency, Onset, and Severity in 677 Patients.
Traschütz A; Adarmes-Gomez AD; Anheim M; Baets J; Falkenburger BH; Gburek-Augustat J; Doss S; Kamm C; Klivenyi P; Grobe-Einsler M; Klopstock T; Minnerop M; Münchau A; Pane C; Renaud M; Santorelli FM; Schöls L; Timmann D; Vielhaber S; Haack TB; van de Warrenburg BP; Zanni G; Synofzik M
Mov Disord; 2023 Jun; 38(6):1109-1112. PubMed ID: 37027459
[No Abstract] [Full Text] [Related]
54. Adult onset sporadic ataxias: a diagnostic challenge.
Barsottini OG; Albuquerque MV; Braga-Neto P; Pedroso JL
Arq Neuropsiquiatr; 2014 Mar; 72(3):232-40. PubMed ID: 24676442
[TBL] [Abstract][Full Text] [Related]
55. NEFL N98S mutation: another cause of dominant intermediate Charcot-Marie-Tooth disease with heterogeneous early-onset phenotype.
Berciano J; Peeters K; García A; López-Alburquerque T; Gallardo E; Hernández-Fabián A; Pelayo-Negro AL; De Vriendt E; Infante J; Jordanova A
J Neurol; 2016 Feb; 263(2):361-369. PubMed ID: 26645395
[TBL] [Abstract][Full Text] [Related]
56. Non-progressive congenital ataxia with cerebellar hypoplasia in three families.
Yapici Z; Eraksoy M
Acta Paediatr; 2005 Feb; 94(2):248-53. PubMed ID: 15981765
[TBL] [Abstract][Full Text] [Related]
57. Concurrence of multiple sclerosis, oligodendroglioma, and autosomal recessive cerebellar ataxia with spasticity in the same patient: A challenging diagnosis.
Algahtani H; Shirah B; Tashkandi M; Samkari A
Mult Scler Relat Disord; 2020 May; 40():101945. PubMed ID: 31954225
[TBL] [Abstract][Full Text] [Related]
58. Ataxia with oculomotor apraxia type 2: not always an easy diagnosis.
Mignarri A; Tessa A; Federico A; Santorelli FM; Dotti MT
Neurol Sci; 2015 Aug; 36(8):1505-7. PubMed ID: 25787807
[No Abstract] [Full Text] [Related]
59. Nosology, genetics, and epidemiology of hereditary ataxias, with particular reference to the epidemiology to these disorders in western Norway.
Refsum S; Skre H
Adv Neurol; 1978; 19():497-508. PubMed ID: 369332
[No Abstract] [Full Text] [Related]
60. Autosomal recessive non-progressive ataxia with an early childhood debut.
Kvistad PH; Dahl A; Skre H
Acta Neurol Scand; 1985 Apr; 71(4):295-302. PubMed ID: 4003033
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
