1. A Novel Duplication in ATXN2 as Modifier for Spinocerebellar Ataxia 3 (SCA3) and C9ORF72‐ALS. Issue 2 (15th October 2020) Authors: Laffita‐Mesa, Jose Miguel; Nennesmo, Inger; Paucar, Martin; Svenningsson, Per Journal: Movement disorders Issue: Volume 36:Issue 2(2021) Page Start: 508 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Adult-Onset Ataxia With Neuropathy and White Matter Abnormalities Due to a Novel SAMD9L Variant. (28th December 2021) Authors: Paucar, Martin; Tesi, Bianca; Eshtad, Saeed; Eriksson, Caroline; Hashim, Farouk; Nilsson, Daniel; Pourhamidi, Kaveh; Hellström-Lindberg, Eva; Bryceson, Yenan T.; Svenningsson, Per Journal: Neurology Issue: Volume 7:Number 6(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Adult-Onset Ataxia With Neuropathy and White Matter Abnormalities Due to a Novel SAMD9L Variant. (December 2021) Authors: Paucar, Martin; Tesi, Bianca; Eshtad, Saeed; Eriksson, Caroline; Hashim, Farouk; Nilsson, Daniel; Pourhamidi, Kaveh; Hellström-Lindberg, Eva; Bryceson, Yenan T.; Svenningsson, Per Journal: Neurology Issue: Volume 7:Number 6(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Altered CSF levels of monoamines in hereditary spastic paraparesis 10: A case series. (August 2019) Authors: Andréasson, Mattias; Lagerstedt-Robinson, Kristina; Samuelsson, Kristin; Solders, Göran; Blennow, Kaj; Paucar, Martin; Svenningsson, Per Journal: Neurology Issue: Volume 5:Number 4(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Ataxin-2 gene: a powerful modulator of neurological disorders. Issue 4 (August 2021) Authors: Laffita-Mesa, Jose Miguel; Paucar, Martin; Svenningsson, Per Journal: Current opinion in neurology Issue: Volume 34:Issue 4(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Chorea, psychosis, acanthocytosis, and prolonged survival associated with ELAC2 mutations. (9th October 2018) Authors: Paucar, Martin; Pajak, Aleksandra; Freyer, Christoph; Bergendal, Åsa; Döry, Margit; Laffita-Mesa, José Miguel; Stranneheim, Henrik; Lagerstedt-Robinson, Kristina; Savitcheva, Irina; Walker, Ruth H.; Wedell, Anna; Wredenberg, Anna; Svenningsson, Per Journal: Neurology Issue: Volume 91:Number 15(2018) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Clinical and genetic characteristics of late-onset Huntington's disease. (April 2019) Authors: Bachoud-Lévi, Anne-Catherine; Bentivoglio, Anna-Rita; Biunno, Ida; Bonelli, Raphael M.; Bronzova, Juliana; Burgunder, Jean-Marc; Dunnett, Stephen B.; Ferreira, Joaquim J.; Frich, Jan; Giuliano, Joe; Handley, Olivia J.; Heiberg, Arvid; Illarioshkin, Sergey; Illmann, Torsten; Klempir, Jiri; Landweh... Journal: Parkinsonism & related disorders Issue: Volume 61(2019) Page Start: 101 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Clinical Reasoning: Leg weakness and stiffness at the emergency room. (5th February 2019) Authors: af Edholm, Karolina; Lidman, Christer; Andersson, Sören; Solders, Göran; Paucar, Martin Journal: Neurology Issue: Volume 92:Number 6(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Concomitant Facioscapulohumeral Muscular Dystrophy and Parkinsonism Mimicking Multiple System Atrophy. Issue 2 (20th October 2015) Authors: Paucar, Martin; Beniaminov, Stanislav; Solders, Göran; Svenningsson, Per Journal: Movement disorders clinical practice Issue: Volume 3:Issue 2(2016:Jun.) Page Start: 194 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Expanding the ataxia with oculomotor apraxia type 4 phenotype. (February 2016) Authors: Paucar, Martin; Malmgren, Helena; Taylor, Malcolm; Reynolds, John J.; Svenningsson, Per; Press, Rayomand; Nordgren, Ann Journal: Neurology Issue: Volume 2:Number 1(2016) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗