311 related articles for article (PubMed ID: 3445070)
41. Magnetic resonance imaging in "typical" and "late onset" Friedreich's disease and early onset cerebellar ataxia with retained tendon reflexes.
De Michele G; Di Salle F; Filla A; D'Alessio G; Ambrosio G; Viscardi L; Scala R; Campanella G
Ital J Neurol Sci; 1995 Jun; 16(5):303-8. PubMed ID: 8537218
[TBL] [Abstract][Full Text] [Related]
42. [Electroencephalographic changes in Firedreich's and Pierre-Marie disease].
Salaeva ZM; Gasanov IaK; Magalov ShI
Zh Nevropatol Psikhiatr Im S S Korsakova; 1975; 75(6):836-9. PubMed ID: 1217384
[TBL] [Abstract][Full Text] [Related]
43. Genetic approaches to the nosology of nervous system defects.
Becker PE
Birth Defects Orig Artic Ser; 1971 Feb; 7(1):10-22. PubMed ID: 5173354
[TBL] [Abstract][Full Text] [Related]
44. Friedreich's ataxia and scoliosis: the experience at two institutions.
Milbrandt TA; Kunes JR; Karol LA
J Pediatr Orthop; 2008 Mar; 28(2):234-8. PubMed ID: 18388721
[TBL] [Abstract][Full Text] [Related]
45. [Electrooculography findings in Friedreich's ataxia].
Prim-Espada MP; de Diego-Sastre JI; Martínez-Salio A; de Sarriá-Lucas MJ
Rev Neurol; 2005 Jan 16-31; 40(2):78-80. PubMed ID: 15712159
[TBL] [Abstract][Full Text] [Related]
46. GAA repeat polymorphism in Turkish Friedreich's ataxia patients.
Yilmaz MB; Koç AF; Kasap H; Güzel AI; Sarica Y; Süleymanova D
Int J Neurosci; 2006 May; 116(5):565-74. PubMed ID: 16644517
[TBL] [Abstract][Full Text] [Related]
47. An autosomal recessive cerebellar ataxia syndrome with upward gaze palsy, neuropathy, and seizures.
Straussberg R; Basel-Vanagaite L; Kivity S; Dabby R; Cirak S; Nurnberg P; Voit T; Mahajnah M; Inbar D; Saifi GM; Lupski JR; Delague V; Megarbane A; Richter A; Leshinsky E; Berkovic SF
Neurology; 2005 Jan; 64(1):142-4. PubMed ID: 15642921
[TBL] [Abstract][Full Text] [Related]
48. 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]
49. [Proposed clinical rating scale for spino-cerebellar ataxia].
De Falco FA; Mansi D; Ventola F; Filla A; Campanella G
Acta Neurol Quad (Napoli); 1979; 39():103-9. PubMed ID: 555225
[No Abstract] [Full Text] [Related]
50. Autosomal recessive ataxia caused by three distinct gene defects in a single consanguineous family.
Bouhlal Y; Zouari M; Kefi M; Ben Hamida C; Hentati F; Amouri R
J Neurogenet; 2008; 22(2):139-48. PubMed ID: 18569450
[TBL] [Abstract][Full Text] [Related]
51. Genetic analysis of early onset cerebellar ataxia with retained tendon reflexes in four Tunisian families.
Marzouki N; Belal S; Benhamida C; Benlemlih M; Hentati F
Clin Genet; 2001 Apr; 59(4):257-62. PubMed ID: 11298681
[TBL] [Abstract][Full Text] [Related]
52. Epidemiological, clinical, paraclinical and molecular study of a cohort of 102 patients affected with autosomal recessive progressive cerebellar ataxia from Alsace, Eastern France: implications for clinical management.
Anheim M; Fleury M; Monga B; Laugel V; Chaigne D; Rodier G; Ginglinger E; Boulay C; Courtois S; Drouot N; Fritsch M; Delaunoy JP; Stoppa-Lyonnet D; Tranchant C; Koenig M
Neurogenetics; 2010 Feb; 11(1):1-12. PubMed ID: 19440741
[TBL] [Abstract][Full Text] [Related]
53. [Epidemiology and clinical polymorphism of hereditary ataxia].
Shutov AA; Dedik GK
Zh Nevropatol Psikhiatr Im S S Korsakova; 1978; 78(6):825-30. PubMed ID: 676607
[TBL] [Abstract][Full Text] [Related]
54. Magnetic resonance imaging in degenerative ataxic disorders.
Ormerod IE; Harding AE; Miller DH; Johnson G; MacManus D; du Boulay EP; Kendall BE; Moseley IF; McDonald WI
J Neurol Neurosurg Psychiatry; 1994 Jan; 57(1):51-7. PubMed ID: 8301305
[TBL] [Abstract][Full Text] [Related]
55. [Distribution of dominant hereditary ataxias and Friedreich's ataxia in the Spanish population].
Mayo Cabrero D; Hernández Cristóbal J; Cantarero Duque S; Martínez Delgado B; Urioste Azcorra M; Robledo Batanero M; García-Ruiz Espiga P; Benítez Ortiz J
Med Clin (Barc); 2000 Jun; 115(4):121-5. PubMed ID: 10996881
[TBL] [Abstract][Full Text] [Related]
56. Prevalence and pattern of spinocerebellar degenerations in northeastern Libya.
Sridharan R; Radhakrishnan K; Ashok PP; Mousa ME
Brain; 1985 Dec; 108 ( Pt 4)():831-43. PubMed ID: 4075075
[TBL] [Abstract][Full Text] [Related]
57. Distinct phenotypes within autosomal recessive ataxias not linked to already known loci.
Bouhlal Y; El-Euch-Fayeche G; Amouri R; Hentati F
Acta Myol; 2005 Oct; 24(2):155-61. PubMed ID: 16550933
[TBL] [Abstract][Full Text] [Related]
58. Hereditary ataxias and paraplegias in Cantabria, Spain. An epidemiological and clinical study.
Polo JM; Calleja J; Combarros O; Berciano J
Brain; 1991 Apr; 114 ( Pt 2)():855-66. PubMed ID: 2043954
[TBL] [Abstract][Full Text] [Related]
59. 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]
60. Friedreich's Ataxia 1978--an overview.
Barbeau A
Can J Neurol Sci; 1978 Feb; 5(1):161-5. PubMed ID: 647493
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
