Now showing items 1-4 of 4

  • Sumathipala, Dulika S; Abeysekera, Gayan S; Jayasekara, Rohan W; Tallaksen, Chantal M; Dissanayake, Vajira H (Journal article / Tidsskriftartikkel / PublishedVersion; Peer reviewed, 2013)
    Background Spinocerebellar ataxias (SCA) are a group of hereditary neurodegenerative disorders. Prevalence of SCA subtypes differ worldwide. Autosomal dominant ataxias are the commonest types of inherited ...
  • Koht, Jeanette; Løstegaard, Sven O; Wedding, Iselin; Vidailhet, Marie; Louha, Malek; Tallaksen, Chantal M (Journal article / Tidsskriftartikkel / PublishedVersion; Peer reviewed, 2016)
    Background Benign hereditary chorea is a rare disorder which is characterized by early onset, non-progressive choreic movement disturbance, with other hyperkinetic movements and unsteadiness also commonly ...
  • Wedding, Iselin M; Kroken, Mette; Henriksen, Sandra P; Selmer, Kaja K; Fiskerstrand, Torunn; Knappskog, Per M; Berge, Tone; Tallaksen, Chantal M (Journal article / Tidsskriftartikkel / PublishedVersion; Peer reviewed, 2015)
    Background Friedreich ataxia is an autosomal recessive hereditary spinocerebellar disorder, characterized by progressive limb and gait ataxia due to proprioceptive loss, often complicated by cardiomyopathy, ...
  • Heimdal, Ketil; Sanchez-Guixé, Monica; Aukrust, Ingvild; Bollerslev, Jens; Bruland, Ove; Jablonski, Greg E; Erichsen, Anne K; Gude, Einar; Koht, Jeanette A; Erdal, Sigrid; Fiskerstrand, Torunn; Haukanes, Bjørn I; Boman, Helge; Bjørkhaug, Lise; Tallaksen, Chantal M; Knappskog, Per M; Johansson, Stefan (Journal article / Tidsskriftartikkel / PublishedVersion; Peer reviewed, 2014)
    Background A subset of hereditary cerebellar ataxias is inherited as autosomal recessive traits (ARCAs). Classification of recessive ataxias due to phenotypic differences in the cerebellum and cerebellar ...