Anders Oldfors
0000-0002-5758-7397
Publication & Citation Trends
Publications
0 total
Incidence and Prevalence of Congenital Myopathies ‐ A Population‐Based Study From Western Sweden
Cited by 1
Semantic Scholar
Exercise intolerance in a large multigeneration family associated with a homoplasmic mitochondrial DNA mutation in MT-TL1
Cited by 0
Semantic Scholar
Novel GYG1 mutation causing late-onset polyglucosan body myopathy with nemaline rods
Cited by 0
Semantic Scholar
G.P.184
Cited by 0
Semantic Scholar
P.15.12 Tubular aggregate myopathy caused by a heterozygous missense mutation in STIM1
Cited by 0
Semantic Scholar
P.15.8 Hereditary myopathy with early respiratory failure (HMERF) – Rapid increase of identified titinopathy families worldwide
Cited by 0
Semantic Scholar
P.16.13 Myopathy with typical OPMD morphology without association with the PABPN1 gene locus
Cited by 0
Semantic Scholar
C.P.9 A novel dynamin-2 gene mutation associated with a late-onset centronuclear myopathy with unusual clinical presentation and necklace fibres
Cited by 0
Semantic Scholar
Research Topics
Mitochondrial Function and Pathology
(130)
Muscle Physiology and Disorders
(119)
Metabolism and Genetic Disorders
(109)
Cardiomyopathy and Myosin Studies
(99)
Neurogenetic and Muscular Disorders Research
(70)
Affiliations
Linköping University
Western University
National Academy of Medicine
Mayo Clinic
Uppsala University Hospital