Wibrand F - Search Results

1

Mutations in COA3 cause isolated complex IV deficiency associated with neuropathy, exercise intolerance, obesity, and short stature.

Ostergaard E, Weraarpachai W, Ravn K, Born AP, Jønson L, Duno M, Wibrand F, Shoubridge EA, Vissing J. Ostergaard E, et al. Among authors: wibrand f. J Med Genet. 2015 Mar;52(3):203-7. doi: 10.1136/jmedgenet-2014-102914. Epub 2015 Jan 20. J Med Genet. 2015. PMID: 25604084

2

Multisystem disorder associated with a missense mutation in the mitochondrial cytochrome b gene.

Wibrand F, Ravn K, Schwartz M, Rosenberg T, Horn N, Vissing J. Wibrand F, et al. Ann Neurol. 2001 Oct;50(4):540-3. doi: 10.1002/ana.1224. Ann Neurol. 2001. PMID: 11601507

3

An mtDNA mutation, 14453G-->A, in the NADH dehydrogenase subunit 6 associated with severe MELAS syndrome.

Ravn K, Wibrand F, Hansen FJ, Horn N, Rosenberg T, Schwartz M. Ravn K, et al. Among authors: wibrand f. Eur J Hum Genet. 2001 Oct;9(10):805-9. doi: 10.1038/sj.ejhg.5200712. Eur J Hum Genet. 2001. PMID: 11781695

4

Multiple mtDNA deletions with features of MNGIE.

Vissing J, Ravn K, Danielsen ER, Dunø M, Wibrand F, Wevers RA, Schwartz M. Vissing J, et al. Among authors: wibrand f. Neurology. 2002 Sep 24;59(6):926-9. doi: 10.1212/wnl.59.6.926. Neurology. 2002. PMID: 12297582

5

[Mitochondrial diseases. Clinical features, investigation and genetics].

Østergaard E, Wibrand F, Horn N, Brøndum-Nielsen K. Østergaard E, et al. Among authors: wibrand f. Ugeskr Laeger. 2003 Feb 10;165(7):663-8. Ugeskr Laeger. 2003. PMID: 12617042 Review. Danish.

6

Late onset of stroke-like episode associated with a 3256C-->T point mutation of mitochondrial DNA.

Jeppesen TD, Schwartz M, Hansen K, Danielsen ER, Wibrand F, Vissing J. Jeppesen TD, et al. Among authors: wibrand f. J Neurol Sci. 2003 Oct 15;214(1-2):17-20. doi: 10.1016/s0022-510x(03)00168-0. J Neurol Sci. 2003. PMID: 12972383

7

Impaired energy metabolism and abnormal muscle histology in mut- methylmalonic aciduria.

Østergaard E, Wibrand F, Ørngreen MC, Vissing J, Horn N. Østergaard E, et al. Among authors: wibrand f. Neurology. 2005 Sep 27;65(6):931-3. doi: 10.1212/01.wnl.0000176065.80560.26. Neurology. 2005. PMID: 16186538

8

Hypertrichosis in patients with SURF1 mutations.

Ostergaard E, Bradinova I, Ravn SH, Hansen FJ, Simeonov E, Christensen E, Wibrand F, Schwartz M. Ostergaard E, et al. Among authors: wibrand f. Am J Med Genet A. 2005 Nov 1;138(4):384-8. doi: 10.1002/ajmg.a.30972. Am J Med Genet A. 2005. PMID: 16222681

9

Aerobic training is safe and improves exercise capacity in patients with mitochondrial myopathy.

Jeppesen TD, Schwartz M, Olsen DB, Wibrand F, Krag T, Dunø M, Hauerslev S, Vissing J. Jeppesen TD, et al. Among authors: wibrand f. Brain. 2006 Dec;129(Pt 12):3402-12. doi: 10.1093/brain/awl149. Epub 2006 Jun 30. Brain. 2006. PMID: 16815877

10

Muscle phenotype and mutation load in 51 persons with the 3243A>G mitochondrial DNA mutation.

Jeppesen TD, Schwartz M, Frederiksen AL, Wibrand F, Olsen DB, Vissing J. Jeppesen TD, et al. Among authors: wibrand f. Arch Neurol. 2006 Dec;63(12):1701-6. doi: 10.1001/archneur.63.12.1701. Arch Neurol. 2006. PMID: 17172609

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