397 related articles for article (PubMed ID: 15779173)
1. [Friedreich's disease in the department of neurology in Dakar].
Ndiaye M; Ndao AK; Sene-Diouf F; Diop AG; Diagne M; Thiam A; Ndiaye MM; Ndiaye IP
Dakar Med; 2000; 45(2):151-3. PubMed ID: 15779173
[TBL] [Abstract][Full Text] [Related]
2. Nerve conduction study, electromyography and somatosensory evoked potentials in non-Friedreich early onset cerebellar ataxia. A comparative study with Friedreich's ataxia and late onset cerebellar ataxia.
Mondelli M; Decchi B; Parlanti S; Scarpini C; Rossi A
Electromyogr Clin Neurophysiol; 1992; 32(4-5):207-14. PubMed ID: 1600884
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. [Hereditary degenerative spinocerebellar diseases in Tunisia with manometric studies in bladder disorders (author's transl)].
Ben Hamida M; Madani S; Zmerli S; Chami I; Annabi A; Jamoussi M; Marzouki M; Rachdi M; Samoud S; Talbi M
Rev Neurol (Paris); 1980; 136(8-9):495-508. PubMed ID: 7221327
[TBL] [Abstract][Full Text] [Related]
5. [Cardiac involvement in Friedreich's heredo-ataxia].
Bertoni PD; Canziani R; Cozzi G; Arancio F; Marforio S
G Ital Cardiol; 1986 Jan; 16(1):22-9. PubMed ID: 2940141
[TBL] [Abstract][Full Text] [Related]
6. Identification and sizing of GAA trinucleotide repeat expansion, investigation for D-loop variations and mitochondrial deletions in Iranian patients with Friedreich's ataxia.
Houshmand M; Panahi MS; Nafisi S; Soltanzadeh A; Alkandari FM
Mitochondrion; 2006 Apr; 6(2):82-8. PubMed ID: 16581313
[TBL] [Abstract][Full Text] [Related]
7. [Clinical and genetic analysis of 188 families with spinocerebellar degeneration. Friedreich's disease and P. Marie's hereditary ataxias].
Ben Hamida M; Attia-Romdhane N; Triki CH; Oueslati S; Hentati F
Rev Neurol (Paris); 1991; 147(12):798-808. PubMed ID: 1780608
[TBL] [Abstract][Full Text] [Related]
8. [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]
9. Pseudodominant Friedreich's ataxia with phenotypic heterogeneity.
Panas M; Kalfakis N; Vassilopoulos D
Acta Neurol Scand; 2007 May; 115(5):364-6. PubMed ID: 17489949
[TBL] [Abstract][Full Text] [Related]
10. Early onset hereditary spinocerebellar ataxia: an autosomal recessive disorder distinct from Friedreich's ataxia.
Kumar D; Blank CE
Indian Pediatr; 1989 Oct; 26(10):1014-9. PubMed ID: 2630444
[TBL] [Abstract][Full Text] [Related]
11. Biological and clinical characteristics of the European Friedreich's Ataxia Consortium for Translational Studies (EFACTS) cohort: a cross-sectional analysis of baseline data.
Reetz K; Dogan I; Costa AS; Dafotakis M; Fedosov K; Giunti P; Parkinson MH; Sweeney MG; Mariotti C; Panzeri M; Nanetti L; Arpa J; Sanz-Gallego I; Durr A; Charles P; Boesch S; Nachbauer W; Klopstock T; Karin I; Depondt C; vom Hagen JM; Schöls L; Giordano IA; Klockgether T; Bürk K; Pandolfo M; Schulz JB
Lancet Neurol; 2015 Feb; 14(2):174-82. PubMed ID: 25566998
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. [Genetic tests: how far should we go? A case of late-onset Friedreich's disease].
Ruolt I; Tranchant C; Warter JM
Rev Neurol (Paris); 2000 Dec; 156(12):1148-50. PubMed ID: 11139731
[TBL] [Abstract][Full Text] [Related]
14. Different phenotypes of Friedreich's ataxia within one 'pseudo-dominant' genealogy: relationships between trinucleotide (GAA) repeat lengths and clinical features.
Illarioshkin SN; Bagieva GK; Klyushnikov SA; Ovchinnikov IV; Markova ED; Ivanova-Smolenskaya IA
Eur J Neurol; 2000 Sep; 7(5):535-40. PubMed ID: 11054139
[TBL] [Abstract][Full Text] [Related]
15. [Electrophysiologic studies (auditory and somatosensory evoked potentials) in Friedreich's ataxia].
Rossi L; Bindi A; De Scisciolo G; Russo G; Marini P; Zappoli R
Riv Patol Nerv Ment; 1984; 105(4):173-85. PubMed ID: 6571600
[TBL] [Abstract][Full Text] [Related]
16. [Friedreich's disease. Clinical study of ten cases (author's transl)].
Fábregues I; Pineda M; Fernández-Alvarez E
Med Clin (Barc); 1980 Apr; 74(8):301-8. PubMed ID: 7374233
[TBL] [Abstract][Full Text] [Related]
17. [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]
18. 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]
19. [Early auditory evoked potentials in spinocerebellar heredodegenerative involvement].
Belkahia A; Ben H'mida M; Ben Jelloul N; Gassab A; Chakroun A
Ann Otolaryngol Chir Cervicofac; 1985; 102(2):97-103. PubMed ID: 4004026
[TBL] [Abstract][Full Text] [Related]
20. Friedreich's ataxia cardiomyopathy: case based discussion and management issues.
Hanley A; Corrigan R; Mohammad S; MacMahon B
Ir Med J; 2010 Apr; 103(4):117-8. PubMed ID: 20486316
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
