Till startsida
Sitemap
To content Read more about how we use cookies on gu.se

Mar Tulinius

Professor/ chief physician

Mar Tulinius
Professor/ chief physician
mar.tulinius@gu.se
+46 31-343 4780

Postal Address: Rondvägen 10, 41685 Göteborg
Visiting Address: Drottning silvias su/östra , 41685 Göteborg


Department of Pediatrics at Institute of Clinical Sciences (More Information)
Drottning Silvias Barn O ungdomsjukh
416 85 Göteborg
Visiting Address: Drottning Silvias Barn O ungdomsjukh , 416 85 Göteborg

Latest publications

Safety and effectiveness of ataluren: comparison of results from the STRIDE Registry and CINRG DMD Natural History Study
E. Mercuri, F. Muntoni, A. N. Osorio, M. Tulinius, F. Buccella et al.
Journal of Comparative Effectiveness Research, Journal article 2020
Journal article

Ataluren use in patients with nonsense mutation Duchenne muscular dystrophy: patient demographics and characteristics from the STRIDE Registry
F. Muntoni, I. Desguerre, M. Guglieri, A. N. Osorio, J. Kirschner et al.
Journal of Comparative Effectiveness Research, Journal article 2019
Journal article

Quality of life of patients with spinal muscular atrophy: A systematic review
E. Landfeldt, J. Edström, T. Sejersen, Mar Tulinius, H. Lochmüller et al.
European Journal of Paediatric Neurology, Review article 2019
Review article

NFL is a marker of treatment response in children with SMA treated with nusinersen
Bob Olsson, L. Alberg, Nicholas C Cullen, Eva Michael, Lisa Wahlgren et al.
Journal of Neurology, Journal article 2019
Journal article

A multinational study on motor function in early-onset FSHD.
Jean K Mah, Jia Feng, Marni B Jacobs, Tina Duong, Kate Carroll et al.
Neurology, Journal article 2018
Journal article

Nusinersen versus Sham Control in Later-Onset Spinal Muscular Atrophy
E. Mercuri, B. T. Darras, C. A. Chiriboga, J. W. Day, C. Campbell et al.
New England Journal of Medicine, Journal article 2018
Journal article

Showing 31 - 40 of 105

2014

Ataluren treatment of patients with nonsense mutation dystrophinopathy.
Katharine Bushby, Richard Finkel, Brenda Wong, Richard Barohn, Craig Campbell et al.
Muscle & nerve, Journal article 2014
Journal article

Electrophysiological, genetic, and ophthalmological findings in children
Susann Andersson, Åkebrand R, Antovan Seyedi Honarvar , Niklas Darin, Mar Tulinius et al.
ISCEV, Boston, USA, 20-24 juli 2014. Poster., Poster 2014
Poster

A multicenter study on Leigh syndrome: disease course and predictors of survival.
Kalliopi Sofou, Irenaeus F M De Coo, Pirjo Isohanni, Elsebet Ostergaard, Karin Naess et al.
Orphanet journal of rare diseases, Journal article 2014
Journal article

Childhood onset tubular aggregate myopathy associated with de novo STIM1 mutations.
Carola Hedberg, Marcello Niceta, Fabiana Fattori, Björn Lindvall, Andrea Ciolfi et al.
Journal of neurology, Journal article 2014
Journal article

2013

Isolated complex I deficiency and atypical clinical courses in three patients due to novel mutations in NDUFS1 and NDUFV1
Kristoffer Björkman, Kalliopi Sofou, Niklas Darin, Gittan Kollberg, Elisabeth Holme et al.
European Journal of Paediatric Neurology. 10th EPNS Congress 25-28 September 2013, Brussels, Belgium, Conference contribution 2013
Conference contribution

The 6-minute walk test and other endpoints in Duchenne muscular dystrophy: longitudinal natural history observations over 48 weeks from a multicenter study.
Craig M McDonald, Erik K Henricson, R Ted Abresch, Julaine M Florence, Michelle Eagle et al.
Muscle & nerve, Journal article 2013
Journal article

Showing 31 - 40 of 105

Page Manager: Katarina Olinder Eriksson|Last update: 10/1/2013
Share:

The University of Gothenburg uses cookies to provide you with the best possible user experience. By continuing on this website, you approve of our use of cookies.  What are cookies?