823 related articles for article (PubMed ID: 23931821)
1. Peripheral nerve involvement in hereditary cerebellar and multisystem degenerative disorders.
Berciano J; García A; Infante J
Handb Clin Neurol; 2013; 115():907-32. PubMed ID: 23931821
[TBL] [Abstract][Full Text] [Related]
2. [Neuroimaging study with morphometric analysis of hereditary and idiopathic ataxia].
Villanueva-Haba V; Garcés-Sánchez M; Bataller L; Palau F; Vílchez J
Neurologia; 2001 Mar; 16(3):105-11. PubMed ID: 11333779
[TBL] [Abstract][Full Text] [Related]
3. [Autosomal recessive cerebellar ataxias].
Anheim M
Rev Neurol (Paris); 2011 May; 167(5):372-84. PubMed ID: 21087783
[TBL] [Abstract][Full Text] [Related]
4. Magnetic resonance imaging in hereditary and idiopathic ataxia.
Wüllner U; Klockgether T; Petersen D; Naegele T; Dichgans J
Neurology; 1993 Feb; 43(2):318-25. PubMed ID: 8437696
[TBL] [Abstract][Full Text] [Related]
5. Phenotypic features and genetic findings in sacsin-related autosomal recessive ataxia in Tunisia.
El Euch-Fayache G; Lalani I; Amouri R; Turki I; Ouahchi K; Hung WY; Belal S; Siddique T; Hentati F
Arch Neurol; 2003 Jul; 60(7):982-8. PubMed ID: 12873855
[TBL] [Abstract][Full Text] [Related]
6. ADC mapping of neurodegeneration in the brainstem and cerebellum of patients with progressive ataxias.
Della Nave R; Foresti S; Tessa C; Moretti M; Ginestroni A; Gavazzi C; Guerrini L; Salvi F; Piacentini S; Mascalchi M
Neuroimage; 2004 Jun; 22(2):698-705. PubMed ID: 15193598
[TBL] [Abstract][Full Text] [Related]
7. Linkage to chromosome 13q11-12 of an autosomal recessive cerebellar ataxia in a Tunisian family.
Mrissa N; Belal S; Hamida CB; Amouri R; Turki I; Mrissa R; Hamida MB; Hentati F
Neurology; 2000 Apr; 54(7):1408-14. PubMed ID: 10751248
[TBL] [Abstract][Full Text] [Related]
8. [Molecular genetics of inherited neuropathies].
Takashima H
Rinsho Shinkeigaku; 2006 Jan; 46(1):1-18. PubMed ID: 16541790
[TBL] [Abstract][Full Text] [Related]
9. Early onset cerebellar ataxia with retained tendon reflexes (EOCA): an electromyographic study.
Pal PK; Taly AB; Nagaraja D; Rao S
Electromyogr Clin Neurophysiol; 1996; 36(5):287-93. PubMed ID: 8877321
[TBL] [Abstract][Full Text] [Related]
10. Cerebral blood flow in spinocerebellar degenerations: a single photon emission tomography study in 28 patients.
De Michele G; Mainenti PP; Soricelli A; Di Salle F; Salvatore E; Longobardi MR; Postiglione A; Salvatore M; Filla A
J Neurol; 1998 Sep; 245(9):603-8. PubMed ID: 9758299
[TBL] [Abstract][Full Text] [Related]
11. Primary degenerative cerebellar ataxias in ethnic Bengalees in West Bengal: some observations.
Chakravarty A; Mukherjee SC
Neurol India; 2003 Jun; 51(2):227-34. PubMed ID: 14571010
[TBL] [Abstract][Full Text] [Related]
12. Olivopontocerebellar atrophy: toward a better nosological definition.
Berciano J; Boesch S; Pérez-Ramos JM; Wenning GK
Mov Disord; 2006 Oct; 21(10):1607-13. PubMed ID: 16874757
[TBL] [Abstract][Full Text] [Related]
13. Multimodal evoked potentials in multiple system and late onset cerebellar atrophies.
Arpa J; López-Pajares R; Cruz-Martínez A; Palomo F; Ferrer T; Caminero AB; Rodríguez-Albariño A; Alonso M; Lacasa T; Nos J
Neurologia; 1995; 10(7):288-96. PubMed ID: 7576727
[TBL] [Abstract][Full Text] [Related]
14. Motor evoked potentials by magnetic stimulation in hereditary and sporadic ataxia.
Mondelli M; Rossi A; Scarpini C; Guazzi GC
Electromyogr Clin Neurophysiol; 1995 Nov; 35(7):415-24. PubMed ID: 8549432
[TBL] [Abstract][Full Text] [Related]
15. Peripheral nerve involvement in spinocerebellar ataxias.
van de Warrenburg BP; Notermans NC; Schelhaas HJ; van Alfen N; Sinke RJ; Knoers NV; Zwarts MJ; Kremer BP
Arch Neurol; 2004 Feb; 61(2):257-61. PubMed ID: 14967775
[TBL] [Abstract][Full Text] [Related]
16. Autosomal recessive cerebellar ataxias.
Palau F; Espinós C
Orphanet J Rare Dis; 2006 Nov; 1():47. PubMed ID: 17112370
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Progressive cerebellar atrophy: hereditary ataxias and disorders with spinocerebellar degeneration.
Wolf NI; Koenig M
Handb Clin Neurol; 2013; 113():1869-78. PubMed ID: 23622410
[TBL] [Abstract][Full Text] [Related]
19. [Clinical features and molecular genetics of autosomal recessive spinocerebellar degenerations].
Tsuji S
Rinsho Shinkeigaku; 2004 Nov; 44(11):785-7. PubMed ID: 15651291
[TBL] [Abstract][Full Text] [Related]
20. [Study on argyrophilic inclusions of multisystem atrophy (Oppenheimer)].
Iwabuchi K; Kosaka K; Haga C; Tuchiya K; Amano N; Itoh K; Yagishita S; Mizutani Y
No To Shinkei; 1991 Jun; 43(6):561-8. PubMed ID: 1654964
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
