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262 results
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Glycogen pathways in disease: new developments in a classical field of medical genetics.
Kilimann MW, Oldfors A. Kilimann MW, et al. Among authors: oldfors a. J Inherit Metab Dis. 2015 May;38(3):483-7. doi: 10.1007/s10545-014-9785-5. Epub 2014 Nov 7. J Inherit Metab Dis. 2015. PMID: 25376534 Review.
New insights in the field of muscle glycogenoses.
Oldfors A, DiMauro S. Oldfors A, et al. Curr Opin Neurol. 2013 Oct;26(5):544-53. doi: 10.1097/WCO.0b013e328364dbdc. Curr Opin Neurol. 2013. PMID: 23995275 Review.
Cardiomyopathy and exercise intolerance in muscle glycogen storage disease 0.
Kollberg G, Tulinius M, Gilljam T, Ostman-Smith I, Forsander G, Jotorp P, Oldfors A, Holme E. Kollberg G, et al. Among authors: oldfors a. N Engl J Med. 2007 Oct 11;357(15):1507-14. doi: 10.1056/NEJMoa066691. N Engl J Med. 2007. PMID: 17928598
Cardiomyopathy as presenting sign of glycogenin-1 deficiency-report of three cases and review of the literature.
Hedberg-Oldfors C, Glamuzina E, Ruygrok P, Anderson LJ, Elliott P, Watkinson O, Occleshaw C, Abernathy M, Turner C, Kingston N, Murphy E, Oldfors A. Hedberg-Oldfors C, et al. Among authors: oldfors a. J Inherit Metab Dis. 2017 Jan;40(1):139-149. doi: 10.1007/s10545-016-9978-1. Epub 2016 Oct 7. J Inherit Metab Dis. 2017. PMID: 27718144 Free PMC article.
A new muscle glycogen storage disease associated with glycogenin-1 deficiency.
Malfatti E, Nilsson J, Hedberg-Oldfors C, Hernandez-Lain A, Michel F, Dominguez-Gonzalez C, Viennet G, Akman HO, Kornblum C, Van den Bergh P, Romero NB, Engel AG, DiMauro S, Oldfors A. Malfatti E, et al. Among authors: oldfors a. Ann Neurol. 2014 Dec;76(6):891-8. doi: 10.1002/ana.24284. Epub 2014 Oct 31. Ann Neurol. 2014. PMID: 25272951 Free PMC article.
Inclusion body myositis: genetic factors, aberrant protein expression, and autoimmunity.
Oldfors A, Fyhr IM. Oldfors A, et al. Curr Opin Rheumatol. 2001 Nov;13(6):469-75. doi: 10.1097/00002281-200111000-00003. Curr Opin Rheumatol. 2001. PMID: 11698722 Review.
Anti-T-lymphocyte globulin treatment in inclusion body myositis: a randomized pilot study.
Lindberg C, Trysberg E, Tarkowski A, Oldfors A. Lindberg C, et al. Among authors: oldfors a. Neurology. 2003 Jul 22;61(2):260-2. doi: 10.1212/01.wnl.0000071852.27182.c7. Neurology. 2003. PMID: 12874415 Clinical Trial.
Inclusion body myositis.
Oldfors A, Lindberg C. Oldfors A, et al. Curr Opin Neurol. 1999 Oct;12(5):527-33. doi: 10.1097/00019052-199910000-00006. Curr Opin Neurol. 1999. PMID: 10590889 Review.
Cardiomyopathy in children with mitochondrial disease; clinical course and cardiological findings.
Holmgren D, Wåhlander H, Eriksson BO, Oldfors A, Holme E, Tulinius M. Holmgren D, et al. Among authors: oldfors a. Eur Heart J. 2003 Feb;24(3):280-8. doi: 10.1016/s0195-668x(02)00387-1. Eur Heart J. 2003. PMID: 12590906
The incidence of mitochondrial encephalomyopathies in childhood: clinical features and morphological, biochemical, and DNA abnormalities.
Darin N, Oldfors A, Moslemi AR, Holme E, Tulinius M. Darin N, et al. Among authors: oldfors a. Ann Neurol. 2001 Mar;49(3):377-83. Ann Neurol. 2001. PMID: 11261513
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