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2. Bone mineral density in patients with multiple sclerosis, hereditary ataxia or hereditary spastic paraplegia after at least 10 years of disease - a case control study. Issue 1 (December 2016)

3. Clinical and genetic characteristics of sporadic adult-onset degenerative ataxia. (5th September 2017)

4. Exon deletions of SPG4 are a frequent cause of hereditary spastic paraplegia. Issue 4 (10th November 2006)

6. Screening for Fabry disease and Hereditary ATTR amyloidosis in idiopathic small‐fiber and mixed neuropathy. Issue 3 (4th December 2018)

7. Survival and severity in dominant cerebellar ataxias. (7th January 2015)

8. VAV1 and BAFF, via NFκB pathway, are genetic risk factors for myasthenia gravis. (11th April 2014)