Wibrand F - Search Results

1

SCA28: Novel Mutation in the AFG3L2 Proteolytic Domain Causes a Mild Cerebellar Syndrome with Selective Type-1 Muscle Fiber Atrophy.

Svenstrup K, Nielsen TT, Aidt F, Rostgaard N, Duno M, Wibrand F, Vinther-Jensen T, Law I, Vissing J, Roos P, Hjermind LE, Nielsen JE. Svenstrup K, et al. Among authors: wibrand f. Cerebellum. 2017 Feb;16(1):62-67. doi: 10.1007/s12311-016-0765-1. Cerebellum. 2017. PMID: 26868664

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

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

4

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

5

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

6

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

7

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

8

31P-MRS of skeletal muscle is not a sensitive diagnostic test for mitochondrial myopathy.

Jeppesen TD, Quistorff B, Wibrand F, Vissing J. Jeppesen TD, et al. Among authors: wibrand f. J Neurol. 2007 Jan;254(1):29-37. doi: 10.1007/s00415-006-0229-5. Epub 2007 Feb 4. J Neurol. 2007. PMID: 17278044

9

Mitochondrial encephalomyopathy with elevated methylmalonic acid is caused by SUCLA2 mutations.

Ostergaard E, Hansen FJ, Sorensen N, Duno M, Vissing J, Larsen PL, Faeroe O, Thorgrimsson S, Wibrand F, Christensen E, Schwartz M. Ostergaard E, et al. Among authors: wibrand f. Brain. 2007 Mar;130(Pt 3):853-61. doi: 10.1093/brain/awl383. Epub 2007 Feb 7. Brain. 2007. PMID: 17287286

10

Deficiency of the alpha subunit of succinate-coenzyme A ligase causes fatal infantile lactic acidosis with mitochondrial DNA depletion.

Ostergaard E, Christensen E, Kristensen E, Mogensen B, Duno M, Shoubridge EA, Wibrand F. Ostergaard E, et al. Among authors: wibrand f. Am J Hum Genet. 2007 Aug;81(2):383-7. doi: 10.1086/519222. Epub 2007 Jun 4. Am J Hum Genet. 2007. PMID: 17668387 Free PMC article.

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