-A Oldfors Researcher Activity Profile

Research Author Detailed Information 

A Oldfors Publication Rate By Year

A Oldfors has published 4 paper(s) in 2003, 4 paper(s) in 2005, 1 paper(s) in 2006, 8 paper(s) in 2007, 1 paper(s) in 2008, for a total of 18 research publications in total.

A A Oldfors Author Information

LAST NAME: oldfors

FIRST NAME: A

INITIALS: a

AFFILIATION:

Papers

A Oldfors's Publication Record

1. Muscle cell and motor protein function in patients with a IIa myosin missense mutation (Glu-706 to Lys). Year Published: 2006
Department of Clinical Neurophysiology, Uppsala University, Uppsala SE-75185, Sweden.
2. Myosin storage myopathy with cardiomyopathy. Year Published: 2007
3. Inflammation and response to steroid treatment in limb-girdle muscular dystrophy 2I. Year Published: 2007
4. Inflammation and response to steroid treatment in limb-girdle muscular dystrophy 2I. Year Published: 2007
5. Leigh syndrome with cytochrome-c oxidase deficiency and a single T insertion nt 5537 in the mitochondrial tRNATrp gene. Year Published: 2003
6. Genotypes and clinical phenotypes in children with cytochrome-c oxidase deficiency. Year Published: 2003
7. Two new mutations in the MTATP6 gene associated with Leigh syndrome. Year Published: 2005
8. Myosin storage myopathy with cardiomyopathy. Year Published: 2007
9. MELAS syndrome in a patient with a point mutation in MTTS1. Year Published: 2008
10. Leigh syndrome with cytochrome-c oxidase deficiency and a single T insertion nt 5537 in the mitochondrial tRNATrp gene. Year Published: 2003
11. Genotypes and clinical phenotypes in children with cytochrome-c oxidase deficiency. Year Published: 2003
12. Two new mutations in the MTATP6 gene associated with Leigh syndrome. Year Published: 2005
13. Inflammation and response to steroid treatment in limb-girdle muscular dystrophy 2I. Year Published: 2007
Department of Pediatrics, Sahlgrenska University Hospital, Göteborg, Sweden. niklas.darin@vgregion.se
14. Alzheimer pathology associated with POLG1 mutation, multiple mtDNA deletions, and APOE4/4: premature ageing or just coincidence? Year Published: 2005
15. Effects of a R133W beta-tropomyosin mutation on regulation of muscle contraction in single human muscle fibres. Year Published: 2007
Department of Clinical Neurophysiology, Uppsala University Hospital, Entrance 85, 3rd floor, SE-751 85 Uppsala, Sweden. julien.ochala@neurofys.uu.se
16. Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy. Year Published: 2007
17. Congenital myopathy with nemaline rods and cap structures caused by a mutation in the beta-tropomyosin gene (TPM2). Year Published: 2007
18. Alzheimer pathology associated with POLG1 mutation, multiple mtDNA deletions, and APOE4/4: premature ageing or just coincidence? Year Published: 2005