Found: 12
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Clinical and genetic studies in a family with a novel mutation in the sepiapterin reductase gene.
- Published in:
- Acta Neurologica Scandinavica: Supplementum, 2014, v. 129, p. 7, doi. 10.1111/ane.12230
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- Article
Ataxia with vitamin E deficiency in southeast Norway, case report.
- Published in:
- Acta Neurologica Scandinavica: Supplementum, 2009, v. 120, p. 42, doi. 10.1111/j.1600-0404.2009.01214.x
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- Article
SPG11 – the most common type of recessive spastic paraplegia in Norway?
- Published in:
- Acta Neurologica Scandinavica: Supplementum, 2008, v. 117, p. 46, doi. 10.1111/j.1600-0404.2008.01031.x
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- Article
Cerebellar ataxia in the eastern and southern parts of Norway.
- Published in:
- Acta Neurologica Scandinavica: Supplementum, 2007, v. 115, p. 76, doi. 10.1111/j.1600-0404.2007.00853.x
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- Publication type:
- Article
Clinical and genetic studies in a family with a novel mutation in the sepiapterin reductase gene.
- Published in:
- Acta Neurologica Scandinavica, 2014, v. 129, p. 7, doi. 10.1111/ane.12230
- By:
- Publication type:
- Article
SCA14 in Norway, two families with autosomal dominant cerebellar ataxia and a novel mutation in the PRKCG gene.
- Published in:
- Acta Neurologica Scandinavica, 2012, v. 125, n. 2, p. 116, doi. 10.1111/j.1600-0404.2011.01504.x
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- Article
An up-date on health-related quality of life in myasthenia gravis -results from population based cohorts.
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- Health & Quality of Life Outcomes, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s12955-015-0298-1
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- Article
A founder mutation p.H701P identified as a major cause of SPG7 in Norway.
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- European Journal of Neurology, 2016, v. 23, n. 4, p. 763, doi. 10.1111/ene.12937
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- Article
Smoking and socio-economic status may affect myasthenia gravis.
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- European Journal of Neurology, 2013, v. 20, n. 3, p. 453, doi. 10.1111/j.1468-1331.2012.03843.x
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- Article
EFNS guidelines on the molecular diagnosis of ataxias and spastic paraplegias.
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- European Journal of Neurology, 2010, v. 17, n. 2, p. 179, doi. 10.1111/j.1468-1331.2009.02873.x
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- Article
EFNS guidelines on the molecular diagnosis of mitochondrial disorders.
- Published in:
- European Journal of Neurology, 2009, v. 16, n. 12, p. 1255, doi. 10.1111/j.1468-1331.2009.02811.x
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- Publication type:
- Article
Seven novel mutations and four exon deletions in a collection of Norwegian patients with SPG4 hereditary spastic paraplegia.
- Published in:
- European Journal of Neurology, 2007, v. 14, n. 7, p. 809, doi. 10.1111/j.1468-1331.2007.01861.x
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- Article