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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 131 - 136 of 136

2004

Parkinsonism, premature menopause, and mitochondrial DNA polymerase gamma mutations: clinical and molecular genetic study
Petri Luoma, Atle Melberg, J. O. Rinne, J. A. Kaukonen, N. N. Nupponen et al.
Lancet, Journal article 2004
Journal article

2003

Myosin storage myopathy associated with a heterozygous missense mutation in MYH7.
Homa Tajsharghi, Lars-Eric Thornell, Christopher Lindberg, Björn Lindvall, Karl-Gösta Henriksson et al.
Annals of neurology, Journal article 2003
Journal article

2002

2000

Autosomal dominant myopathy: missense mutation (Glu-706 --> Lys) in the myosin heavy chain IIa gene.
Tommy Martinsson, Anders Oldfors, Niklas Darin, Kerstin Berg, Homa Tajsharghi et al.
Proceedings of the National Academy of Sciences of the United States of America, Journal article 2000
Journal article

Showing 131 - 136 of 136

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