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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 81 - 90 of 136


A novel homozygous RRM2B missense mutation in association with severe mtDNA depletion.
Gittan Kollberg, Niklas Darin, Karin Benan, Ali-Reza Moslemi, Sigurd Lindal et al.
Neuromuscular disorders : NMD, Journal article 2009
Journal article

Molecular basis of infantile reversible cytochrome c oxidase deficiency myopathy.
Rita Horvath, John P Kemp, Helen A L Tuppen, Gavin Hudson, Anders Oldfors et al.
Brain : a journal of neurology, Journal article 2009
Journal article

A patient with two mitochondrial DNA mutations causing PEO and LHON.
Atle Melberg, Ali-Reza Moslemi, Oscar Palm, Raili Raininko, Erik Stålberg et al.
European journal of medical genetics, Journal article 2009
Journal article

"Necklace" fibers, a new histological marker of late-onset MTM1-related centronuclear myopathy.
Jorge A Bevilacqua, Marc Bitoun, Valérie Biancalana, Anders Oldfors, Gisela Stoltenburg et al.
Acta neuropathologica, Journal article 2009
Journal article


New morphologic and genetic findings in cap disease associated with beta-tropomyosin (TPM2) mutations.
Monica Ohlsson, S Quijano-Roy, Niklas Darin, G Brochier, E Lacène et al.
Neurology, Journal article 2008
Journal article

Thick filament diseases
Anders Oldfors, Phillipa Lamont
In: The Sarcomere and skeletal muscle disease. Laing N (Ed) Series: Advances in Experimental Medicine and Biology Series Editors: Back N, Cohen IR, Lajtha A, Lambris JD, Paoletti R. Volume 642, New York, Landes Bioscience and Springer , Chapter in book 2008
Chapter in book

Showing 81 - 90 of 136

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

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