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Anders Oldfors

Anställd

Anders Oldfors

anders.oldfors@pathology.gu.se
+46 31-342 2084
0707-338116

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 11 - 20 of 136

2018

Polyglucosan myopathy and functional characterization of a novel GYG1 mutation
Carola Oldfors Hedberg, A. Mensch, Kittichate Visuttijai, G. Stoltenburg, D. Stoevesandt et al.
Acta Neurologica Scandinavica, Journal article 2018
Journal article

2017

Myopathology in the times of modern genetics.
Markus Schuelke, Nancy Christine Øien, Anders Oldfors
Neuropathology and applied neurobiology, Review article 2017
Review article

Cardiomyopathy as presenting sign of glycogenin-1 deficiency-report of three cases and review of the literature.
Carola Oldfors Hedberg, Emma Glamuzina, Peter Ruygrok, Lisa J Anderson, Perry Elliott et al.
Journal of inherited metabolic disease, Journal article 2017
Journal article

2016

Leukoencephalopathy due to Complex II Deficiency and Bi-Allelic SDHB Mutations: Further Cases and Implications for Genetic Counselling.
Sabine Grønborg, Niklas Darin, Maria J Miranda, Bodil Damgaard, Jorge Asin-Cayuela et al.
JIMD reports, Journal article 2016
Journal article

A new early-onset neuromuscular disorder associated with kyphoscoliosis peptidase (KY) deficiency.
Carola Oldfors Hedberg, Niklas Darin, Mia Olsson Engman, Zacharias Orfanos, Christer Thomsen et al.
European journal of human genetics : EJHG, Journal article 2016
Journal article

Showing 11 - 20 of 136

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