817 related articles for article (PubMed ID: 18787576)
41. Update on degenerative ataxias.
Klockgether T
Curr Opin Neurol; 2011 Aug; 24(4):339-45. PubMed ID: 21734495
[TBL] [Abstract][Full Text] [Related]
42. Clinical and genetic epidemiological study of 16q22.1-linked autosomal dominant cerebellar ataxia in western Japan.
Hayashi M; Adachi Y; Mori M; Nakano T; Nakashima K
Acta Neurol Scand; 2007 Aug; 116(2):123-7. PubMed ID: 17661799
[TBL] [Abstract][Full Text] [Related]
43. [Molecular genetics and familial ataxia].
Koenig M; Sirugo G; Duclos F
Rev Neurol (Paris); 1993; 149(11):698-702. PubMed ID: 8091082
[TBL] [Abstract][Full Text] [Related]
44. Autosomal recessive cerebellar ataxias: the current state of affairs.
Vermeer S; van de Warrenburg BP; Willemsen MA; Cluitmans M; Scheffer H; Kremer BP; Knoers NV
J Med Genet; 2011 Oct; 48(10):651-9. PubMed ID: 21856962
[TBL] [Abstract][Full Text] [Related]
45. [Eye movement disorders in hereditary degenerative ataxia. Electro-oculographic study of 11 cases].
Serlenga L; Falco F; Castaldo V; Caldarazzo M; Federici A
Acta Neurol (Napoli); 1992; 14(4-6):440-50. PubMed ID: 1293987
[TBL] [Abstract][Full Text] [Related]
46. Evoked potential abnormalities in the various inherited ataxias.
Nuwer MR; Perlman SL; Packwood JW; Kark RA
Ann Neurol; 1983 Jan; 13(1):20-7. PubMed ID: 6830160
[TBL] [Abstract][Full Text] [Related]
47. Clinical and genetic characterizations of 16q-linked autosomal dominant spinocerebellar ataxia (AD-SCA) and frequency analysis of AD-SCA in the Japanese population.
Nozaki H; Ikeuchi T; Kawakami A; Kimura A; Koide R; Tsuchiya M; Nakmura Y; Mutoh T; Yamamoto H; Nakao N; Sahashi K; Nishizawa M; Onodera O
Mov Disord; 2007 Apr; 22(6):857-62. PubMed ID: 17357132
[TBL] [Abstract][Full Text] [Related]
48. Patterns of fractional anisotropy changes in white matter of cerebellar peduncles distinguish spinocerebellar ataxia-1 from multiple system atrophy and other ataxia syndromes.
Prakash N; Hageman N; Hua X; Toga AW; Perlman SL; Salamon N
Neuroimage; 2009 Aug; 47 Suppl 2():T72-81. PubMed ID: 19446636
[TBL] [Abstract][Full Text] [Related]
49. Rare forms of autosomal recessive neurodegenerative ataxia.
Koenig M
Semin Pediatr Neurol; 2003 Sep; 10(3):183-92. PubMed ID: 14653406
[TBL] [Abstract][Full Text] [Related]
50. [Spinocerebellar ataxia 7. Clinical and genetic investigation in an Argentine family].
Rojas JI; Romano M; Patrucco L; Zurru MC; Igarreta P; Cristiano E
Medicina (B Aires); 2007; 67(2):147-50. PubMed ID: 17593599
[TBL] [Abstract][Full Text] [Related]
51. Late-onset Friedreich ataxia: phenotypic analysis, magnetic resonance imaging findings, and review of the literature.
Bhidayasiri R; Perlman SL; Pulst SM; Geschwind DH
Arch Neurol; 2005 Dec; 62(12):1865-9. PubMed ID: 16344344
[TBL] [Abstract][Full Text] [Related]
52. Recent advances in degenerative ataxias.
Klockgether T
Curr Opin Neurol; 2000 Aug; 13(4):451-5. PubMed ID: 10970064
[TBL] [Abstract][Full Text] [Related]
53. [Have centers of rare neurological diseases changed their practices and management of the hereditary cerebellar ataxias?].
Tranchant C
Rev Neurol (Paris); 2013 Feb; 169 Suppl 1():S23-7. PubMed ID: 23452767
[TBL] [Abstract][Full Text] [Related]
54. Quantification of circulating plasma DNA in Friedreich's ataxia and spinocerebellar ataxia types 2 and 12.
Swarup V; Srivastava AK; Padma MV; Rajeswari MR
DNA Cell Biol; 2011 Jun; 30(6):389-94. PubMed ID: 21329459
[TBL] [Abstract][Full Text] [Related]
55. Deciphering the causes of sporadic late-onset cerebellar ataxias: a prospective study with implications for diagnostic work.
Gebus O; Montaut S; Monga B; Wirth T; Cheraud C; Alves Do Rego C; Zinchenko I; Carré G; Hamdaoui M; Hautecloque G; Nguyen-Them L; Lannes B; Chanson JB; Lagha-Boukbiza O; Fleury MC; Devys D; Nicolas G; Rudolf G; Bereau M; Mallaret M; Renaud M; Acquaviva C; Koenig M; Koob M; Kremer S; Namer IJ; Cazeneuve C; Echaniz-Laguna A; Tranchant C; Anheim M
J Neurol; 2017 Jun; 264(6):1118-1126. PubMed ID: 28478596
[TBL] [Abstract][Full Text] [Related]
56. Prevalence of inherited ataxias in the province of Padua, Italy.
Zortea M; Armani M; Pastorello E; Nunez GF; Lombardi S; Tonello S; Rigoni MT; Zuliani L; Mostacciuolo ML; Gellera C; Di Donato S; Trevisan CP
Neuroepidemiology; 2004; 23(6):275-80. PubMed ID: 15297793
[TBL] [Abstract][Full Text] [Related]
57. Cerebellar ataxias.
Manto M; Marmolino D
Curr Opin Neurol; 2009 Aug; 22(4):419-29. PubMed ID: 19421057
[TBL] [Abstract][Full Text] [Related]
58. The inherited cerebellar ataxias: an update.
Coarelli G; Wirth T; Tranchant C; Koenig M; Durr A; Anheim M
J Neurol; 2023 Jan; 270(1):208-222. PubMed ID: 36152050
[TBL] [Abstract][Full Text] [Related]
59. [Ataxias in children. Clinical and genetic aspects].
Goutieres F
J Genet Hum; 1981 Sep; 29(3):211-20. PubMed ID: 6801195
[No Abstract] [Full Text] [Related]
60. [Cardiac manifestations of Friedreich's ataxia].
Kolek M; Mrózek V; Schenk P
Cas Lek Cesk; 2004; 143(1):48-51. PubMed ID: 15061120
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]