125 related articles for article (PubMed ID: 12244769)
1. [Diagnosis: not more than an agreement on disease entity].
van Gijn J; Walvoort HC
Ned Tijdschr Geneeskd; 2002 Sep; 146(36):1672-4. PubMed ID: 12244769
[TBL] [Abstract][Full Text] [Related]
2. [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]
3. 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]
4. [Friedrich's ataxia: clinical difficulties and genetic possibilities].
van de Warrenburg BP; Knoers NV; Kremer HP
Ned Tijdschr Geneeskd; 2002 Sep; 146(36):1669-72. PubMed ID: 12244768
[TBL] [Abstract][Full Text] [Related]
5. Friedreich's ataxia mimicking hereditary motor and sensory neuropathy.
Panas M; Kalfakis N; Karadima G; Davaki P; Vassilopoulos D
J Neurol; 2002 Nov; 249(11):1583-6. PubMed ID: 12420100
[TBL] [Abstract][Full Text] [Related]
6. [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]
7. Early onset cerebellar ataxia with retained tendon reflexes: a clinical and genetic study of a disorder distinct from Friedreich's ataxia.
Harding AE
J Neurol Neurosurg Psychiatry; 1981 Jun; 44(6):503-8. PubMed ID: 7276963
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. [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]
10. [Differential diagnosis of Friedreich ataxia].
Claus D
Nervenarzt; 1989 Jan; 60(1):26-31. PubMed ID: 2922087
[TBL] [Abstract][Full Text] [Related]
11. Friedreich's ataxia: clinical heterogeneity in two sisters.
Armani M; Zortea M; Pastorello E; Lombardi S; Tonello S; Zuliani L; Rigoni MT; Trevisan CP
Neurol Sci; 2006 Jun; 27(2):140-2. PubMed ID: 16816915
[TBL] [Abstract][Full Text] [Related]
12. [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]
13. 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]
14. 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]
15. Vitamin E deficiency ataxia with (744 del A) mutation on alpha-TTP gene: genetic and clinical peculiarities in Moroccan patients.
Marzouki N; Benomar A; Yahyaoui M; Birouk N; Elouazzani M; Chkili T; Benlemlih M
Eur J Med Genet; 2005; 48(1):21-8. PubMed ID: 15953402
[TBL] [Abstract][Full Text] [Related]
16. [Hereditary ataxia-problems in the classification, genetics and genetic counseling].
Bachmann H; Lössner J
Z Gesamte Inn Med; 1981 Jun; 36(11):387-93. PubMed ID: 7303765
[TBL] [Abstract][Full Text] [Related]
17. Very-late-onset Friedreich's ataxia: diagnosis in a kindred with late-onset cerebellar ataxia.
Fearon C; Lonergan R; Ferguson D; Byrne S; Bradley D; Langan Y; Redmond J
Pract Neurol; 2020 Feb; 20(1):55-58. PubMed ID: 31467149
[TBL] [Abstract][Full Text] [Related]
18. [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]
19. [Friedreich's ataxia and hereditary vitamin E deficiency. Case study].
Labauge P; Cavalier L; Ichalalène L; Castelnovo G
Rev Neurol (Paris); 1998 May; 154(4):339-41. PubMed ID: 9773063
[TBL] [Abstract][Full Text] [Related]
20. Friedreich ataxia.
Johnson WG
Clin Neurosci; 1995; 3(1):33-8. PubMed ID: 7614092
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]