Tallaksen CM - Search Results

1

SCA14 in Norway, two families with autosomal dominant cerebellar ataxia and a novel mutation in the PRKCG gene.

Koht J, Stevanin G, Durr A, Mundwiller E, Brice A, Tallaksen CM. Koht J, et al. Among authors: tallaksen cm. Acta Neurol Scand. 2012 Feb;125(2):116-22. doi: 10.1111/j.1600-0404.2011.01504.x. Epub 2011 Mar 21. Acta Neurol Scand. 2012. PMID: 21434874

2

Ataxia with vitamin E deficiency in southeast Norway, case report.

Koht J, Bjørnarå KA, Jørum E, Tallaksen CM. Koht J, et al. Among authors: tallaksen cm. Acta Neurol Scand Suppl. 2009;(189):42-5. doi: 10.1111/j.1600-0404.2009.01214.x. Acta Neurol Scand Suppl. 2009. PMID: 19566498

3

Cerebellar ataxia in the eastern and southern parts of Norway.

Koht J, Tallaksen CM. Koht J, et al. Among authors: tallaksen cm. Acta Neurol Scand Suppl. 2007;187:76-9. doi: 10.1111/j.1600-0404.2007.00853.x. Acta Neurol Scand Suppl. 2007. PMID: 17419835

4

SPG11--the most common type of recessive spastic paraplegia in Norway?

Erichsen AK, Stevanin G, Denora P, Brice A, Tallaksen CM. Erichsen AK, et al. Among authors: tallaksen cm. Acta Neurol Scand Suppl. 2008;188:46-50. doi: 10.1111/j.1600-0404.2008.01031.x. Acta Neurol Scand Suppl. 2008. PMID: 18439221

5

Clinical and genetic studies in a family with a novel mutation in the sepiapterin reductase gene.

Koht J, Rengmark A, Opladen T, Bjørnarå KA, Selberg T, Tallaksen CM, Blau N, Toft M. Koht J, et al. Among authors: tallaksen cm. Acta Neurol Scand Suppl. 2014;(198):7-12. doi: 10.1111/ane.12230. Acta Neurol Scand Suppl. 2014. PMID: 24588500

6

Complicated forms of autosomal dominant hereditary spastic paraplegia are frequent in SPG10.

Goizet C, Boukhris A, Mundwiller E, Tallaksen C, Forlani S, Toutain A, Carriere N, Paquis V, Depienne C, Durr A, Stevanin G, Brice A. Goizet C, et al. Hum Mutat. 2009 Feb;30(2):E376-85. doi: 10.1002/humu.20920. Hum Mutat. 2009. PMID: 18853458

7

Factors influencing disease progression in autosomal dominant cerebellar ataxia and spastic paraplegia.

Tezenas du Montcel S, Charles P, Goizet C, Marelli C, Ribai P, Vincitorio C, Anheim M, Guyant-Maréchal L, Le Bayon A, Vandenberghe N, Tchikviladzé M, Devos D, Le Ber I, N'Guyen K, Cazeneuve C, Tallaksen C, Brice A, Durr A. Tezenas du Montcel S, et al. Arch Neurol. 2012 Apr;69(4):500-8. doi: 10.1001/archneurol.2011.2713. Arch Neurol. 2012. PMID: 22491195

8

Cognition is only minimally impaired in Spinocerebellar ataxia type 14 (SCA14): a neuropsychological study of ten Norwegian subjects compared to intrafamilial controls and population norm.

Wedding IM, Koht J, Dietrichs E, Landrø NI, Tallaksen CM. Wedding IM, et al. Among authors: tallaksen cm. BMC Neurol. 2013 Nov 29;13:186. doi: 10.1186/1471-2377-13-186. BMC Neurol. 2013. PMID: 24289098 Free PMC article.

9

Mutation analysis of the paraplegin gene (SPG7) in patients with hereditary spastic paraplegia.

Elleuch N, Depienne C, Benomar A, Hernandez AM, Ferrer X, Fontaine B, Grid D, Tallaksen CM, Zemmouri R, Stevanin G, Durr A, Brice A. Elleuch N, et al. Among authors: tallaksen cm. Neurology. 2006 Mar 14;66(5):654-9. doi: 10.1212/01.wnl.0000201185.91110.15. Neurology. 2006. PMID: 16534102

10

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. Dürr A, et al. Arch Neurol. 2004 Dec;61(12):1867-72. doi: 10.1001/archneur.61.12.1867. Arch Neurol. 2004. PMID: 15596607

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