Lindgren U - Search Results

1

Respiratory chain dysfunction in perifascicular muscle fibres in patients with dermatomyositis is associated with mitochondrial DNA depletion.

Hedberg-Oldfors C, Lindgren U, Visuttijai K, Lööf D, Roos S, Thomsen C, Oldfors A. Hedberg-Oldfors C, et al. Among authors: lindgren u. Neuropathol Appl Neurobiol. 2022 Dec;48(7):e12841. doi: 10.1111/nan.12841. Epub 2022 Aug 6. Neuropathol Appl Neurobiol. 2022. PMID: 35894812 Free PMC article.

2

Mitochondrial DNA depletion in single fibers in a patient with novel TK2 mutations.

Roos S, Lindgren U, Ehrstedt C, Moslemi AR, Oldfors A. Roos S, et al. Among authors: lindgren u. Neuromuscul Disord. 2014 Aug;24(8):713-20. doi: 10.1016/j.nmd.2014.05.009. Epub 2014 May 29. Neuromuscul Disord. 2014. PMID: 24953930

3

Mitochondrial pathology in inclusion body myositis.

Lindgren U, Roos S, Hedberg Oldfors C, Moslemi AR, Lindberg C, Oldfors A. Lindgren U, et al. Neuromuscul Disord. 2015 Apr;25(4):281-8. doi: 10.1016/j.nmd.2014.12.010. Epub 2015 Jan 6. Neuromuscul Disord. 2015. PMID: 25638290

4

Mitochondrial complex IV deficiency caused by a novel frameshift variant in MT-CO2 associated with myopathy and perturbed acylcarnitine profile.

Roos S, Sofou K, Hedberg-Oldfors C, Kollberg G, Lindgren U, Thomsen C, Tulinius M, Oldfors A. Roos S, et al. Among authors: lindgren u. Eur J Hum Genet. 2019 Feb;27(2):331-335. doi: 10.1038/s41431-018-0286-0. Epub 2018 Oct 12. Eur J Hum Genet. 2019. PMID: 30315213 Free PMC article.

5

Progressive external ophthalmoplegia associated with novel MT-TN mutations.

Visuttijai K, Hedberg-Oldfors C, Lindgren U, Nordström S, Elíasdóttir Ó, Lindberg C, Oldfors A. Visuttijai K, et al. Among authors: lindgren u. Acta Neurol Scand. 2021 Jan;143(1):103-108. doi: 10.1111/ane.13339. Epub 2020 Sep 19. Acta Neurol Scand. 2021. PMID: 32869280 Free PMC article.

6

Mitochondrial DNA variants in inclusion body myositis characterized by deep sequencing.

Hedberg-Oldfors C, Lindgren U, Basu S, Visuttijai K, Lindberg C, Falkenberg M, Larsson Lekholm E, Oldfors A. Hedberg-Oldfors C, et al. Among authors: lindgren u. Brain Pathol. 2021 May;31(3):e12931. doi: 10.1111/bpa.12931. Brain Pathol. 2021. PMID: 33354847 Free PMC article.

7

Epidemiology, Survival, and Clinical Characteristics of Inclusion Body Myositis.

Lindgren U, Pullerits R, Lindberg C, Oldfors A. Lindgren U, et al. Ann Neurol. 2022 Aug;92(2):201-212. doi: 10.1002/ana.26412. Epub 2022 Jun 6. Ann Neurol. 2022. PMID: 35596584 Free PMC article.

8

Inclusion body myositis with early onset: a population-based study.

Lindgren U, Hedberg-Oldfors C, Pullerits R, Lindberg C, Oldfors A. Lindgren U, et al. J Neurol. 2023 Nov;270(11):5483-5492. doi: 10.1007/s00415-023-11878-w. Epub 2023 Jul 27. J Neurol. 2023. PMID: 37498322 Free PMC article.

9

272nd ENMC international workshop: 10 Years of progress - revision of the ENMC 2013 diagnostic criteria for inclusion body myositis and clinical trial readiness. 16-18 June 2023, Hoofddorp, The Netherlands.

Lilleker JB, Naddaf E, Saris CGJ, Schmidt J, de Visser M, Weihl CC; 272nd ENMC workshop participants. Lilleker JB, et al. Neuromuscul Disord. 2024 Apr;37:36-51. doi: 10.1016/j.nmd.2024.03.001. Epub 2024 Mar 7. Neuromuscul Disord. 2024. PMID: 38522330

10

Lipid storage myopathy associated with sertraline treatment is an acquired mitochondrial disorder with respiratory chain deficiency.

Hedberg-Oldfors C, Lindgren U, Visuttijai K, Shen Y, Ilinca A, Nordström S, Lindberg C, Oldfors A. Hedberg-Oldfors C, et al. Among authors: lindgren u. Acta Neuropathol. 2024 Nov 26;148(1):73. doi: 10.1007/s00401-024-02830-x. Acta Neuropathol. 2024. PMID: 39586906 Free PMC article.

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