To the top

Page Manager: Webmaster
Last update: 4/19/2017 1:56 PM

Tell a friend about this page
Print version

Carola Hedberg Oldfors - University of Gothenburg, Sweden Till startsida
Sitemap
To content Read more about how we use cookies on gu.se

Carola Hedberg Oldfors

Researcher

Carola Hedberg Oldfors
Researcher
carola.oldfors@gu.se

Postal Address: Box 100, 40530 Göteborg
Visiting Address: Medicinaregatan 3B , 41390 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

Cardiomyopathy with lethal arrhythmias associated with inactivation of KLHL24
Carola Oldfors Hedberg, Alexandra Abramsson, D. P. S. Osborn, O. Danielsson, A. Fazlinezhad et al.
Hum Mol Genet, Journal article 2019
Journal article

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

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

Showing 21 - 30 of 43

2015

Muscle pathology and whole-body MRI in a polyglucosan myopathy associated with a novel glycogenin-1 mutation
S. S. Luo, W. H. Zhu, D. Y. Yue, J. Lin, Y. Wang et al.
Neuromuscular Disorders, Journal article 2015
Journal article

A novel dynamin-2 gene mutation associated with a late-onset centronuclear myopathy with necklace fibres
O. Casar-Borota, J. Jacobsson, R. Libelius, Carola Oldfors Hedberg, E. Malfatti et al.
Neuromuscular Disorders, Journal article 2015
Journal article

2014

A New Muscle Glycogen Storage Disease Associated with Glycogenin-1 Deficiency
Edoardo Malfatti, Johanna Nilsson, Carola Hedberg, A. Hernandez-Lain, F. Michel et al.
Annals of Neurology, Journal article 2014
Journal article

Hereditary myopathy with early respiratory failure: occurrence in various populations.
Johanna Palmio, Anni Evilä, Françoise Chapon, Giorgio Tasca, Fengqing Xiang et al.
Journal of neurology, neurosurgery, and psychiatry, Journal article 2014
Journal article

Childhood onset tubular aggregate myopathy associated with de novo STIM1 mutations.
Carola Hedberg, Marcello Niceta, Fabiana Fattori, Björn Lindvall, Andrea Ciolfi et al.
Journal of neurology, Journal article 2014
Journal article

2013

Reply to Brodehl et al.
Carola Hedberg, Atle Melberg, Angelika Kuhl, Dieter Jenne, Anders Oldfors
European journal of human genetics : EJHG, Magazine article 2013
Magazine article

Showing 21 - 30 of 43

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

The University of Gothenburg uses cookies to provide you with the best possible user experience. By continuing on this website, you approve of our use of cookies.  What are cookies?