Autosomal dominant hereditary ataxia in Sri Lanka

por Sumathipala, Dulika S, Abeysekera, Gayan S, Jayasekara, Rohan W, Tallaksen, Chantal ME, Dissanayake, Vajira HW
Publicado 2013

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

por Wedding, Iselin Marie, Koht, Jeanette, Dietrichs, Espen, Landrø, Nils Inge, Tallaksen, Chantal ME
Publicado 2013

Benign hereditary chorea, not only chorea: a family case presentation

por Koht, Jeanette, Løstegaard, Sven Olav, Wedding, Iselin, Vidailhet, Marie, Louha, Malek, Tallaksen, Chantal ME
Publicado 2016

Friedreich ataxia in Norway – an epidemiological, molecular and clinical study

por Wedding, Iselin Marie, Kroken, Mette, Henriksen, Sandra Pilar, Selmer, Kaja Kristine, Fiskerstrand, Torunn, Knappskog, Per Morten, Berge, Tone, Tallaksen, Chantal ME
Publicado 2015

STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity

por Heimdal, Ketil, Sanchez-Guixé, Monica, Aukrust, Ingvild, Bollerslev, Jens, Bruland, Ove, Jablonski, Greg Eigner, Erichsen, Anne Kjersti, Gude, Einar, Koht, Jeanette A, Erdal, Sigrid, Fiskerstrand, Torunn, Haukanes, Bjørn Ivar, Boman, Helge, Bjørkhaug, Lise, Tallaksen, Chantal ME, Knappskog, Per M, Johansson, Stefan
Publicado 2014