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1951 1
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Page 1
Elisabeth Holme.
Kollberg G, Clayton P. Kollberg G, et al. J Inherit Metab Dis. 2015 Nov;38(6):1159-60. doi: 10.1007/s10545-015-9892-y. J Inherit Metab Dis. 2015. PMID: 26420280 No abstract available.
Mitochondrial abnormalities in inclusion-body myositis.
Oldfors A, Moslemi AR, Jonasson L, Ohlsson M, Kollberg G, Lindberg C. Oldfors A, et al. Among authors: kollberg g. Neurology. 2006 Jan 24;66(2 Suppl 1):S49-55. doi: 10.1212/01.wnl.0000192127.63013.8d. Neurology. 2006. PMID: 16432145 Review.
Characterization and review of MTHFD1 deficiency: four new patients, cellular delineation and response to folic and folinic acid treatment.
Burda P, Kuster A, Hjalmarson O, Suormala T, Bürer C, Lutz S, Roussey G, Christa L, Asin-Cayuela J, Kollberg G, Andersson BA, Watkins D, Rosenblatt DS, Fowler B, Holme E, Froese DS, Baumgartner MR. Burda P, et al. Among authors: kollberg g. J Inherit Metab Dis. 2015 Sep;38(5):863-72. doi: 10.1007/s10545-015-9810-3. Epub 2015 Jan 30. J Inherit Metab Dis. 2015. PMID: 25633902 Free article. Review.
Phenotypic spectrum and clinical course of single large-scale mitochondrial DNA deletion disease in the paediatric population: a multicentre study.
Björkman K, Vissing J, Østergaard E, Bindoff LA, de Coo IFM, Engvall M, Hikmat O, Isohanni P, Kollberg G, Lindberg C, Majamaa K, Naess K, Uusimaa J, Tulinius M, Darin N. Björkman K, et al. Among authors: kollberg g. J Med Genet. 2023 Jan;60(1):65-73. doi: 10.1136/jmedgenet-2021-108006. Epub 2021 Dec 6. J Med Genet. 2023. PMID: 34872991 Free PMC article.
Expression pattern of mitochondrial respiratory chain enzymes in skeletal muscle of patients with mitochondrial myopathy associated with the homoplasmic m.14674T>C variant.
Roos S, Hedberg-Oldfors C, Visuttijai K, Stein M, Kollberg G, Elíasdóttir Ó, Lindberg C, Darin N, Oldfors A. Roos S, et al. Among authors: kollberg g. Brain Pathol. 2022 Jul;32(4):e13038. doi: 10.1111/bpa.13038. Epub 2021 Nov 21. Brain Pathol. 2022. PMID: 34806237 Free PMC article.
Phenotypic and genotypic variability in Alpers syndrome.
Sofou K, Moslemi AR, Kollberg G, Bjarnadóttir I, Oldfors A, Nennesmo I, Holme E, Tulinius M, Darin N. Sofou K, et al. Among authors: kollberg g. Eur J Paediatr Neurol. 2012 Jul;16(4):379-89. doi: 10.1016/j.ejpn.2011.12.006. Epub 2012 Jan 10. Eur J Paediatr Neurol. 2012. PMID: 22237560
37 results