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Anders Oldfors - University of Gothenburg, Sweden Till startsida
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Anders Oldfors


Anders Oldfors
+46 31-342 2084

Postal Address: Box 100, 40530 Göteborg
Visiting Address: Gula stråket 8 , 41345 Göteborg

Department of Laboratory Medicine at Institute of Biomedicine (More Information)
Sahlgrenska universitetssjukhuset
413 45 Göteborg
Visiting Address: Gula stråket 8 , 413 45 Göteborg

Latest publications

Loss of Sarcomeric Scaffolding as a Common Baseline Histopathologic Lesion in Titin-Related Myopathies
R. Ávila-Polo, E. Malfatti, X. Lornage, C. Cheraud, I. Nelson et al.
Journal of Neuropathology and Experimental Neurology, Journal article 2018
Journal article

A novel complex neurological phenotype due to a homozygous mutation in FDX2
J. Gurgel-Giannetti, D. S. Lynch, A. R. B. de Paiva, L. T. Lucato, G. Yamamoto et al.
Brain, Journal article 2018
Journal article

Oxygen consumption in platelets as an adjunct diagnostic method for pediatric mitochondrial disease.
Emil Westerlund, Sigurður E Marelsson, Johannes K Ehinger, Fredrik Sjövall, Saori Morota et al.
Pediatric research, Journal article 2018
Journal article

Showing 61 - 70 of 136


Mutation spectrum in the large GTPase dynamin 2, and genotype-phenotype correlation in autosomal dominant centronuclear myopathy.
Johann Böhm, Valérie Biancalana, Elizabeth T Dechene, Marc Bitoun, Christopher R Pierson et al.
Human mutation, Journal article 2012
Journal article

Phenotypic and genotypic variability in Alpers syndrome.
Kalliopi Sofou, Ali-Reza Moslemi, Gittan Kollberg, Ingibjörg Bjarnadottir, Anders Oldfors et al.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society, Journal article 2012
Journal article

Congenital myasthenic syndrome with tubular aggregates caused by GFPT1 mutations
V. Guergueltcheva, J. Muller, M. Dusl, J. Senderek, Anders Oldfors et al.
Journal of Neurology, Journal article 2012
Journal article


Sporadic centronuclear myopathy with muscle pseudohypertrophy, neutropenia, and necklace fibres due to a DNM2 mutation.
Norma Beatriz Romero, Jorge A Bevilacqua, Anders Oldfors, Michel Fardeau
Neuromuscular disorders : NMD, Magazine article 2011
Magazine article

Hexosamine Biosynthetic Pathway Mutations Cause Neuromuscular Transmission Defect
J Senderek, JS Muller, M Dusl, TM Strom, V Guergueltcheva et al.
American journal of human genetics, Journal article 2011
Journal article

Showing 61 - 70 of 136

Page Manager: Webmaster|Last update: 4/19/2017

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