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Items: 1 to 20 of 691

1.

Prevalence of hereditary ataxia and spastic paraplegia in southeast Norway: a population-based study.

Erichsen AK, Koht J, Stray-Pedersen A, Abdelnoor M, Tallaksen CM.

Brain. 2009 Jun;132(Pt 6):1577-88. doi: 10.1093/brain/awp056. Epub 2009 Mar 31.

PMID:
19339254
2.

Hereditary ataxia and spastic paraplegia in Portugal: a population-based prevalence study.

Coutinho P, Ruano L, Loureiro JL, Cruz VT, Barros J, Tuna A, Barbot C, Guimarães J, Alonso I, Silveira I, Sequeiros J, Marques Neves J, Serrano P, Silva MC.

JAMA Neurol. 2013 Jun;70(6):746-55. doi: 10.1001/jamaneurol.2013.1707.

PMID:
23609960
3.

The global epidemiology of hereditary ataxia and spastic paraplegia: a systematic review of prevalence studies.

Ruano L, Melo C, Silva MC, Coutinho P.

Neuroepidemiology. 2014;42(3):174-83. doi: 10.1159/000358801. Epub 2014 Mar 5. Review.

4.

The prevalence of "pure" autosomal dominant hereditary spastic paraparesis in the island of Ireland.

McMonagle P, Webb S, Hutchinson M.

J Neurol Neurosurg Psychiatry. 2002 Jan;72(1):43-6.

5.

Hereditary ataxias and paraplegias in Valle d'Aosta, Italy: a study of prevalence and disability.

Leone M, Bottacchi E, D'Alessandro G, Kustermann S.

Acta Neurol Scand. 1995 Mar;91(3):183-7.

PMID:
7793232
6.

Prevalence of hereditary ataxias and spastic paraplegias in Molise, a region of Italy.

Filla A, De Michele G, Marconi R, Bucci L, Carillo C, Castellano AE, Iorio L, Kniahynicki C, Rossi F, Campanella G.

J Neurol. 1992 Jul;239(6):351-3.

PMID:
1512613
7.

Hereditary spastic paraplegia: advances in genetic research. Hereditary Spastic Paraplegia Working group.

Fink JK, Heiman-Patterson T, Bird T, Cambi F, Dubé MP, Figlewicz DA, Fink JK, Haines JL, Heiman-Patterson T, Hentati A, Pericak-Vance MA, Raskind W, Rouleau GA, Siddique T.

Neurology. 1996 Jun;46(6):1507-14. Review.

PMID:
8649538
8.

Hereditary ataxias and spastic paraplegias: methodological aspects of a prevalence study in Portugal.

Silva MC, Coutinho P, Pinheiro CD, Neves JM, Serrano P.

J Clin Epidemiol. 1997 Dec;50(12):1377-84.

PMID:
9449941
9.

Atlastin1 mutations are frequent in young-onset autosomal dominant spastic paraplegia.

Dürr A, Camuzat A, Colin E, Tallaksen C, Hannequin D, Coutinho P, Fontaine B, Rossi A, Gil R, Rousselle C, Ruberg M, Stevanin G, Brice A.

Arch Neurol. 2004 Dec;61(12):1867-72.

PMID:
15596607
10.

Autosomal dominant spastic paraplegias: a review of 89 families resulting from a portuguese survey.

Loureiro JL, Brandão E, Ruano L, Brandão AF, Lopes AM, Thieleke-Matos C, Miller-Fleming L, Cruz VT, Barbosa M, Silveira I, Stevanin G, Pinto-Basto J, Sequeiros J, Alonso I, Coutinho P.

JAMA Neurol. 2013 Apr;70(4):481-7. doi: 10.1001/jamaneurol.2013.1956. Review.

PMID:
23400676
11.

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
12.

[The diagnostic course in patients with hereditary ataxias and hereditary spastic paraparesis].

Leone M, Bottacchi E, D'Ambrosio R, Mittino D, Rosso MG, Brignolio F.

Minerva Med. 1992 Jul-Aug;83(7-8):421-6. Italian.

PMID:
1522965
13.

Spastic paraplegia, ataxia, mental retardation (SPAR): a novel genetic disorder.

Hedera P, Rainier S, Zhao XP, Schalling M, Lindblad K, Yuan QP, Ikeuchi T, Trobe J, Wald JJ, Eldevik OP, Kluin K, Fink JK.

Neurology. 2002 Feb 12;58(3):411-6.

PMID:
11839840
14.

The prevalence of hereditary spastic paraplegia and the occurrence of SPG4 mutations in Estonia.

Braschinsky M, Luus SM, Gross-Paju K, Haldre S.

Neuroepidemiology. 2009;32(2):89-93. doi: 10.1159/000177033. Epub 2008 Nov 27.

PMID:
19039240
15.

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.

PMID:
2043954
16.

Three novel mutations of the spastin gene in Chinese patients with hereditary spastic paraplegia.

Tang B, Zhao G, Xia K, Pan Q, Luo W, Shen L, Long Z, Dai H, Zi X, Jiang H.

Arch Neurol. 2004 Jan;61(1):49-55.

PMID:
14732620
17.

[The genetics of movement disorders--spinocerebellar degenerations].

Tallaksen CM, Dietrichs E.

Tidsskr Nor Laegeforen. 2004 Sep 9;124(17):2233-5. Review. Norwegian.

18.
19.

Hereditary spastic paraplegia with hypoplastic corpus callosum in a Turkish family.

Gucuyener K, Hirfanoglu T, Ok I, Cansu A, Serdaroglu A.

J Child Neurol. 2007 Feb;22(2):214-7.

PMID:
17621486
20.

Prevalence of inherited ataxias in the province of Padua, Italy.

Zortea M, Armani M, Pastorello E, Nunez GF, Lombardi S, Tonello S, Rigoni MT, Zuliani L, Mostacciuolo ML, Gellera C, Di Donato S, Trevisan CP.

Neuroepidemiology. 2004 Nov-Dec;23(6):275-80. Epub 2004 Aug 5.

PMID:
15297793

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