Martin Paucar (M Paucar)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 11

Top Venues

Neurology. Genetics

Cerebellum (London, England)

Annals of neurology

Journal of neurovirology

Karolinska Universitetssjukhuset Huddinge

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Karolinska Universitetssjukhuset Huddinge Jan 01 2008 - Jun 30 2016

Sweden

Läkare :: Neurology

Publications

Martin Paucar, Daniel Nilsson, Martin Engvall, José Laffita-Mesa, Anna Wedell, Per Svenningsson
Comment to: "SCA4 Unravelled After More than 25 Years Using Advanced Genomic Technologies". Movement disorders : official journal of the Movement Disorder Society 39 (6) (2024)
Ilan Ben-Shabat, Malin Kvarnung, Wolfgang Sperker, Helene Bruhn, Anna Wredenberg, Rolf Wibom, Inger Nennesmo, Martin Engvall, Martin Paucar
Ataxia Syndrome With Hearing Loss and Nephronophthisis Associated With a Novel Homozygous Variant in XPNPEP3 . Neurology. Genetics 9 (6) (2023)
Martin Paucar, Richard Ågren, Tianyi Li, Simon Lissmats, Åsa Bergendal, Jan Weinberg, Daniel Nilsson, Irina Savichetva, Kristoffer Sahlholm, Johanna Nilsson, Per Svenningsson
V374A KCND3 Pathogenic Variant Associated With Paroxysmal Ataxia Exacerbations. Neurology. Genetics 7 (1) (2021)
Karolina Af Edhom, Christer Lidman, Tobias Granberg, Graham P Taylor, Martin Paucar
Expanding the etiologic spectrum of spastic ataxia syndrome: chronic infection with human T lymphotropic virus type 1. Journal of neurovirology 27 (2) (2021)
Martin Paucar, Håkan Almqvist, Ingemar Björkhem, Per Svenningsson
Hyperkinesias and Echolalia in Primary Familial Brain Calcification. Annals of neurology 89 (2) (2020)
Martin Paucar, J Lundin, T Alshammari, Å Bergendal, M Lindefeldt, M Alshammari, G Solders, J Di Re, I Savitcheva, T Granberg, F Laezza, E Iwarsson, P Svenningsson
Broader phenotypic traits and widespread brain hypometabolism in spinocerebellar ataxia 27. Journal of internal medicine 288 (1) (2020)
Sebastian Thams, Mominul Islam, Marie Lindefeldt, Ann Nordgren, Tobias Granberg, Bianca Tesi, Gisela Barbany, Daniel Nilsson, Martin Paucar
Heterozygous variants in DCC: Beyond congenital mirror movements. Neurology. Genetics 6 (6) (2020)
Martin Paucar, Tobias Granberg, Kristina Lagerstedt-Robinson, Elisabet Waldenlind, Sven Petersson, Love Nordin, Per Svenningsson
SLC1A3 variant associated with hemiplegic migraine and acetazolamide-responsive MRS changes. Neurology. Genetics 6 (4) (2020)
Valter Niemelä, Ammar Salih, Daniela Solea, Björn Lindvall, Jan Weinberg, Gabriel Miltenberger, Tobias Granberg, Aikaterini Tzovla, Love Nordin, Torsten Danfors, Irina Savitcheva, Niklas Dahl, Martin Paucar
Phenotypic variability in chorea-acanthocytosis associated with novel VPS13A mutations. Neurology. Genetics 6 (3) (2020)
Martin Paucar, Åsa Bergendal, Peter Gustavsson, Magnus Nordenskjöld, José Laffita-Mesa, Irina Savitcheva, Per Svenningsson
Novel Features and Abnormal Pattern of Cerebral Glucose Metabolism in Spinocerebellar Ataxia 19. Cerebellum (London, England) 17 (4) (2019)
Humberto Skott, Cristina Muntean-Firanescu, Kristin Samuelsson, Luca Verrecchia, Per Svenningsson, Helena Malmgren, Carmen Cananau, Alberto J Espay, Rayomand Press, Göran Solders, Martin Paucar
The cerebellar phenotype of Charcot-Marie-Tooth neuropathy type 4C. Cerebellum & ataxias 6 (2019)

Martin Paucar.css-eqlu8i{font-size:small;padding-left:4px;} (M Paucar)

Publication Activity (10 Years)

Top Topics

Top Venues

Martin Paucar (M Paucar)