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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 21 - 30 of 105

2015

Early onset cardiomyopathy in females with Danon disease
Carola Oldfors Hedberg, Gyöngyvér Máthé, K. Thomson, Mar Tulinius, Kristjan Karason et al.
Neuromuscular Disorders, Journal article 2015
Journal article

Ophthalmological and genetic findings in children with Leigh syndrome - a long-term follow-up
Susann Andersson, R Åkebrand, Antovan Seyedi Honarvar , Kalliopi Sofou, Niklas Darin et al.
WSPOS (World Society of Paediatric Ophthalmology and Strabismus), Barcelona, Spanien, 3-5 sept 2015., Poster 2015
Poster

Ophthalmological findings in children with Leigh syndrome - a long-term follow-up
Susann Andersson, R Åkebrand, Antovan Seyedi Honarvar , Kalliopi Sofou, Niklas Darin et al.
NPOG, Åland, Finland, 10-12 juni 2015. Föredrag., Conference contribution 2015
Conference contribution

Bengt Hagberg.
Christopher Gillberg, I Carina Gillberg, Peder Rasmussen, Mårten Kyllerman, Elisabeth Fernell et al.
Acta paediatrica (Oslo, Norway : 1992), Magazine article 2015
Magazine article

The TREAT-NMD advisory committee for therapeutics (TACT): an innovative de-risking model to foster orphan drug development.
Emma Heslop, Cristina Csimma, Volker Straub, John McCall, Kanneboyina Nagaraju et al.
Orphanet journal of rare diseases, Journal article 2015
Journal article

Investigating the role of the physiological isoform switch of cytochrome c oxidase subunits in reversible mitochondrial disease
V. Boczonadi, M. Giunta, M. Lane, Mar Tulinius, U. Schara et al.
International Journal of Biochemistry & Cell Biology, Journal article 2015
Journal article

Structural modeling of tissue-specific mitochondrial alanyl-tRNA synthetase (AARS2) defects predicts differential effects on aminoacylation
L. Euro, S. Konovalova, Jorge Asin-Cayuela, Mar Tulinius, H. Griffin et al.
Frontiers in Genetics, Journal article 2015
Journal article

2014

Showing 21 - 30 of 105

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