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Autosomal recessive cerebellar ataxias.

Palau F, Espinós C.

Orphanet J Rare Dis. 2006 Nov 17;1:47. Review.PMID: 17112370 [PubMed - indexed for MEDLINE]Related articlesFree article

[Autosomal recessive cerebellar ataxias. Their classification, genetic features and pathophysiology]

Espinós-Armero C, González-Cabo P, Palau-Martínez F.

Rev Neurol. 2005 Oct 1-15;41(7):409-22. Review. Spanish. PMID: 16193447 [PubMed - indexed for MEDLINE]Related articlesFree article

[Autosomal recessive cerebellar ataxias]

Tranchant C, Anheim M.

Presse Med. 2009 Dec;38(12):1852-9. Epub 2009 May 12. Review. French. PMID: 19442480 [PubMed - indexed for MEDLINE]Related articles

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. Epub 2009 May 14.PMID: 19440741 [PubMed - in process]Related articles

The complex clinical and genetic classification of inherited ataxias. II. Autosomal recessive ataxias.

Di Donato S, Gellera C, Mariotti C.

Neurol Sci. 2001 Jun;22(3):219-28. Review.PMID: 11731874 [PubMed - indexed for MEDLINE]Related articles

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.PMID: 16550933 [PubMed - indexed for MEDLINE]Related articles

Rare forms of autosomal recessive neurodegenerative ataxia.

Koenig M.

Semin Pediatr Neurol. 2003 Sep;10(3):183-92. Review.PMID: 14653406 [PubMed - indexed for MEDLINE]Related articles

Clinical features and molecular genetics of autosomal recessive cerebellar ataxias.

Fogel BL, Perlman S.

Lancet Neurol. 2007 Mar;6(3):245-57. Review.PMID: 17303531 [PubMed - indexed for MEDLINE]Related articles

New autosomal recessive cerebellar ataxias with oculomotor apraxia.

Le Ber I, Brice A, Dürr A.

Curr Neurol Neurosci Rep. 2005 Sep;5(5):411-7. Review.PMID: 16131425 [PubMed - indexed for MEDLINE]Related articles

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.PMID: 11298681 [PubMed - indexed for MEDLINE]Related articles

[Autosomal recessive cerebellar ataxias with oculomotor apraxia]

Le Ber I, Rivaud-Péchoux S, Brice A, Dürr A.

Rev Neurol (Paris). 2006 Feb;162(2):177-84. Review. French. PMID: 16518257 [PubMed - indexed for MEDLINE]Related articles

Recessive ataxia with ocular apraxia: review of 22 Portuguese patients.

Barbot C, Coutinho P, Chorão R, Ferreira C, Barros J, Fineza I, Dias K, Monteiro J, Guimarães A, Mendonça P, do Céu Moreira M, Sequeiros J.

Arch Neurol. 2001 Feb;58(2):201-5.PMID: 11176957 [PubMed - indexed for MEDLINE]Related articlesFree article

Cerebellar ataxia with oculomotor apraxia type 1: clinical and genetic studies.

Le Ber I, Moreira MC, Rivaud-Péchoux S, Chamayou C, Ochsner F, Kuntzer T, Tardieu M, Saïd G, Habert MO, Demarquay G, Tannier C, Beis JM, Brice A, Koenig M, Dürr A.

Brain. 2003 Dec;126(Pt 12):2761-72. Epub 2003 Sep 23.PMID: 14506070 [PubMed - indexed for MEDLINE]Related articlesFree article

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 Apr-Jun;22(2):139-48.PMID: 18569450 [PubMed - indexed for MEDLINE]Related articles

Ataxia with oculomotor apraxia type 1 (AOA1): clinical and neuropsychological features in 2 new patients and differential diagnosis.

D'Arrigo S, Riva D, Bulgheroni S, Chiapparini L, Castellotti B, Gellera C, Pantaleoni C.

J Child Neurol. 2008 Aug;23(8):895-900. Epub 2008 Apr 10.PMID: 18403580 [PubMed - indexed for MEDLINE]Related articles

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.PMID: 4075075 [PubMed - indexed for MEDLINE]Related articles

A novel c.5308_5311delGAGA mutation in Senataxin in a Cypriot family with an autosomal recessive cerebellar ataxia.

Nicolaou P, Georghiou A, Votsi C, Middleton LT, Zamba-Papanicolaou E, Christodoulou K.

BMC Med Genet. 2008 Apr 14;9:28.PMID: 18405395 [PubMed - indexed for MEDLINE]Related articlesFree article

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.PMID: 2630444 [PubMed - indexed for MEDLINE]Related articles

[Recessive hereditary ataxia with early onset. Clinical study of 27 cases]

Serlenga L, Trizio M, Pozio G, Oteri G, Caldarazzo M.

Riv Neurol. 1987 Sep-Oct;57(5):285-9. Italian. PMID: 3445070 [PubMed - indexed for MEDLINE]Related articles

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.PMID: 7276963 [PubMed - indexed for MEDLINE]Related articlesFree article