Fever-related ataxia: a case report of CAPOS syndrome

por Stenshorne, Ida, Rasmussen, Magnhild, Salvanos, Panagiotis, Tallaksen, Chantal M. E., Bindoff, Laurence A., Koht, Jeanette
Publicado 2019

Mild phenotype in an adult male with X‐linked adrenoleukodystrophy – case report

por Horn, Morten A., Mikaelsen, Karin B. M., Ferdinandusse, Sacha, Jørum, Ellen, Mellgren, Svein I., Retterstøl, Lars, Wanders, Ronald J. A., Tallaksen, Chantal M. E.
Publicado 2015

Targeted high throughput sequencing in hereditary ataxia and spastic paraplegia

por Iqbal, Zafar, Rydning, Siri L., Wedding, Iselin M., Koht, Jeanette, Pihlstrøm, Lasse, Rengmark, Aina H., Henriksen, Sandra P., Tallaksen, Chantal M. E., Toft, Mathias
Publicado 2017

Correction: Targeted high throughput sequencing in hereditary ataxia and spastic paraplegia

por Iqbal, Zafar, Rydning, Siri L., Wedding, Iselin M., Koht, Jeanette, Pihlstrøm, Lasse, Rengmark, Aina H., Henriksen, Sandra P., Tallaksen, Chantal M. E., Toft, Mathias
Publicado 2017

Spastic Paraplegia Type 7 Is Associated with Multiple Mitochondrial DNA Deletions

por Wedding, Iselin Marie, Koht, Jeanette, Tran, Gia Tuong, Misceo, Doriana, Selmer, Kaja Kristine, Holmgren, Asbjørn, Frengen, Eirik, Bindoff, Laurence, Tallaksen, Chantal M. E., Tzoulis, Charalampos
Publicado 2014

Biallelic POLR3A variants confirmed as a frequent cause of hereditary ataxia and spastic paraparesis

por Rydning, Siri L, Koht, Jeanette, Sheng, Ying, Sowa, Piotr, Hjorthaug, Hanne S, Wedding, Iselin M, Erichsen, Anne Kjersti, Hovden, Inger Anette, Backe, Paul H, Tallaksen, Chantal M E, Vigeland, Magnus D, Selmer, Kaja K
Publicado 2019

The impact of gender, puberty, and pregnancy in patients with POLG disease

por Hikmat, Omar, Naess, Karin, Engvall, Martin, Klingenberg, Claus, Rasmussen, Magnhild, Tallaksen, Chantal M. E., Samsonsen, Christian, Brodtkorb, Eylert, Ostergaard, Elsebet, de Coo, Rene, Pias‐Peleteiro, Leticia, Isohanni, Pirjo, Uusimaa, Johanna, Darin, Niklas, Rahman, Shamima, Bindoff, Laurence A.
Publicado 2020

Late Onset Myasthenia Gravis Is Associated with HLA DRB1*15:01 in the Norwegian Population

por Maniaol, Angelina H., Elsais, Ahmed, Lorentzen, Åslaug R., Owe, Jone F., Viken, Marte K., Sæther, Hanne, Flåm, Siri T., Bråthen, Geir, Kampman, Margitta T., Midgard, Rune, Christensen, Marte, Rognerud, Anna, Kerty, Emilia, Gilhus, Nils Erik, Tallaksen, Chantal M. E., Lie, Benedicte A., Harbo, Hanne F.
Publicado 2012