160 related articles for article (PubMed ID: 10197066)
21. Early onset cerebellar ataxia with retained tendon reflexes. Clinical, electrophysiological and MRI observations in comparison with Friedreich's ataxia.
Klockgether T; Petersen D; Grodd W; Dichgans J
Brain; 1991 Aug; 114 ( Pt 4)():1559-73. PubMed ID: 1884166
[TBL] [Abstract][Full Text] [Related]
22. Uncommon features in Cuban families affected with Friedreich ataxia.
Cruz-Mariño T; González-Zaldivar Y; Laffita-Mesa JM; Almaguer-Mederos L; Aguilera-Rodríguez R; Almaguer-Gotay D; Rodríguez-Labrada R; Canales-Ochoa N; Macleod P; Velázquez-Pérez L
Neurosci Lett; 2010 Mar; 472(2):85-9. PubMed ID: 20109528
[TBL] [Abstract][Full Text] [Related]
23. [Recessive hereditary ataxia with early onset. Clinical study of 27 cases].
Serlenga L; Trizio M; Pozio G; Oteri G; Caldarazzo M
Riv Neurol; 1987; 57(5):285-9. PubMed ID: 3445070
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. Why do some Friedreich's ataxia patients retain tendon reflexes? A clinical, neurophysiological and molecular study.
Coppola G; De Michele G; Cavalcanti F; Pianese L; Perretti A; Santoro L; Vita G; Toscano A; Amboni M; Grimaldi G; Salvatore E; Caruso G; Filla A
J Neurol; 1999 May; 246(5):353-7. PubMed ID: 10399865
[TBL] [Abstract][Full Text] [Related]
26. Delayed-onset Friedreich's ataxia revisited.
Lecocq C; Charles P; Azulay JP; Meissner W; Rai M; N'Guyen K; Péréon Y; Fabre N; Robin E; Courtois S; Guyant-Maréchal L; Zagnoli F; Rudolf G; Renaud M; Sévin-Allouet M; Lesne F; Alaerts N; Goizet C; Calvas P; Eusebio A; Guissart C; Derkinderen P; Tison F; Brice A; Koenig M; Pandolfo M; Tranchant C; Dürr A; Anheim M
Mov Disord; 2016 Jan; 31(1):62-9. PubMed ID: 26388117
[TBL] [Abstract][Full Text] [Related]
27. Clinical and genetic abnormalities in patients with Friedreich's ataxia.
Dürr A; Cossee M; Agid Y; Campuzano V; Mignard C; Penet C; Mandel JL; Brice A; Koenig M
N Engl J Med; 1996 Oct; 335(16):1169-75. PubMed ID: 8815938
[TBL] [Abstract][Full Text] [Related]
28. Markedly different course of Friedreich's ataxia in sib pairs with similar GAA repeat expansions in the frataxin gene.
Klopstock T; Chahrokh-Zadeh S; Holinski-Feder E; Meindl A; Gasser T; Pongratz D; Müller-Felber W
Acta Neuropathol; 1999 Feb; 97(2):139-42. PubMed ID: 9928824
[TBL] [Abstract][Full Text] [Related]
29. Early onset hereditary ataxias of unknown etiology. Review of a personal series.
Filla A; De Michele G; Barbieri F; Campanella G
Acta Neurol (Napoli); 1992; 14(4-6):420-30. PubMed ID: 1293985
[TBL] [Abstract][Full Text] [Related]
30. Molecular analysis of GAA repeats and four linked bi-allelic markers in and around the frataxin gene in patients and normal populations from India.
Chattopadhyay B; Gupta S; Gangopadhyay PK; Das SK; Roy T; Mukherjee SC; Sinha KK; Singhal BS; Bhattacharyya NP
Ann Hum Genet; 2004 May; 68(Pt 3):189-95. PubMed ID: 15180699
[TBL] [Abstract][Full Text] [Related]
31. Parental gender, age at birth and expansion length influence GAA repeat intergenerational instability in the X25 gene: pedigree studies and analysis of sperm from patients with Friedreich's ataxia.
De Michele G; Cavalcanti F; Criscuolo C; Pianese L; Monticelli A; Filla A; Cocozza S
Hum Mol Genet; 1998 Nov; 7(12):1901-6. PubMed ID: 9811933
[TBL] [Abstract][Full Text] [Related]
32. Trinucleotide (GAA)n repeat expansion in two families with Friedreich's ataxia with retained reflexes.
Kellett MW; Fletcher NA; Wood N; Enevoldson TP
J Neurol Neurosurg Psychiatry; 1997 Dec; 63(6):780-3. PubMed ID: 9416816
[TBL] [Abstract][Full Text] [Related]
33. Typical Friedreich's ataxia without GAA expansions and GAA expansion without typical Friedreich's ataxia.
McCabe DJ; Ryan F; Moore DP; McQuaid S; King MD; Kelly A; Daly K; Barton DE; Murphy RP
J Neurol; 2000 May; 247(5):346-55. PubMed ID: 10896266
[TBL] [Abstract][Full Text] [Related]
34. DNA methylation in intron 1 of the frataxin gene is related to GAA repeat length and age of onset in Friedreich ataxia patients.
Castaldo I; Pinelli M; Monticelli A; Acquaviva F; Giacchetti M; Filla A; Sacchetti S; Keller S; Avvedimento VE; Chiariotti L; Cocozza S
J Med Genet; 2008 Dec; 45(12):808-12. PubMed ID: 18697824
[TBL] [Abstract][Full Text] [Related]
35. The Friedreich's ataxia gene encodes a novel phosphatidylinositol-4- phosphate 5-kinase.
Carvajal JJ; Pook MA; dos Santos M; Doudney K; Hillermann R; Minogue S; Williamson R; Hsuan JJ; Chamberlain S
Nat Genet; 1996 Oct; 14(2):157-62. PubMed ID: 8841185
[TBL] [Abstract][Full Text] [Related]
36. Friedreich ataxia: Detection of GAA repeat expansions and frataxin point mutations.
Pandolfo M
Methods Mol Med; 2006; 126():197-216. PubMed ID: 16930014
[TBL] [Abstract][Full Text] [Related]
37. Early-onset ataxia with cardiomyopathy and retained tendon reflexes maps to the Friedreich's ataxia locus on chromosome 9q.
Palau F; De Michele G; Vilchez JJ; Pandolfo M; Monrós E; Cocozza S; Smeyers P; Lopez-Arlandis J; Campanella G; Di Donato S
Ann Neurol; 1995 Mar; 37(3):359-62. PubMed ID: 7695235
[TBL] [Abstract][Full Text] [Related]
38. [Friedreich's ataxia: recent developments and prospects for treatment].
Legros B; Manto MU
Rev Med Brux; 1999 Apr; 20(2):73-9. PubMed ID: 10335100
[TBL] [Abstract][Full Text] [Related]
39. [Unusual molecular changes in two families with Friedreich's ataxia].
González MC; Díaz-Golpe V; Hernández L; Martin S; Fernández F
Neurologia; 2003 Sep; 18(7):392-5. PubMed ID: 14505249
[TBL] [Abstract][Full Text] [Related]
40. Marked variation in the cardiomyopathy associated with Friedreich's ataxia.
Dutka DP; Donnelly JE; Nihoyannopoulos P; Oakley CM; Nunez DJ
Heart; 1999 Feb; 81(2):141-7. PubMed ID: 9922348
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]