Holme E - Search Results

1

The effect of supervised rehabilitation on strength, postural sway, position sense and re-injury risk after acute ankle ligament sprain.

Holme E, Magnusson SP, Becher K, Bieler T, Aagaard P, Kjaer M. Holme E, et al. Scand J Med Sci Sports. 1999 Apr;9(2):104-9. doi: 10.1111/j.1600-0838.1999.tb00217.x. Scand J Med Sci Sports. 1999. PMID: 10220845 Clinical Trial.

2

Temperature responses to electrically induced cycling in spinal cord injured persons.

Holme E, Mohr T, Kjaer M, Nielsen B. Holme E, et al. Med Sci Sports Exerc. 2001 Mar;33(3):431-5. doi: 10.1097/00005768-200103000-00015. Med Sci Sports Exerc. 2001. PMID: 11252070

3

A novel missense mutation in SUCLG1 associated with mitochondrial DNA depletion, encephalomyopathic form, with methylmalonic aciduria.

Ostergaard E, Schwartz M, Batbayli M, Christensen E, Hjalmarson O, Kollberg G, Holme E. Ostergaard E, et al. Among authors: holme e. Eur J Pediatr. 2010 Feb;169(2):201-5. doi: 10.1007/s00431-009-1007-z. Epub 2009 Jun 14. Eur J Pediatr. 2010. PMID: 19526370

4

ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency.

Olsen RK, Olpin SE, Andresen BS, Miedzybrodzka ZH, Pourfarzam M, Merinero B, Frerman FE, Beresford MW, Dean JC, Cornelius N, Andersen O, Oldfors A, Holme E, Gregersen N, Turnbull DM, Morris AA. Olsen RK, et al. Among authors: holme e. Brain. 2007 Aug;130(Pt 8):2045-54. doi: 10.1093/brain/awm135. Epub 2007 Jun 20. Brain. 2007. PMID: 17584774

5

A novel mitochondrial tRNA Arg mutation resulting in an anticodon swap in a patient with mitochondrial encephalomyopathy.

Roos S, Darin N, Kollberg G, Andersson Grönlund M, Tulinius M, Holme E, Moslemi AR, Oldfors A. Roos S, et al. Among authors: holme e. Eur J Hum Genet. 2013 May;21(5):571-3. doi: 10.1038/ejhg.2012.153. Epub 2012 Jul 11. Eur J Hum Genet. 2013. PMID: 22781096 Free PMC article.

6

Novel mutations in the thymidine kinase 2 gene (TK2) associated with fatal mitochondrial myopathy and mitochondrial DNA depletion.

Tulinius M, Moslemi AR, Darin N, Holme E, Oldfors A. Tulinius M, et al. Among authors: holme e. Neuromuscul Disord. 2005 Jun;15(6):412-5. doi: 10.1016/j.nmd.2005.03.010. Neuromuscul Disord. 2005. PMID: 15907288

7

A novel homozygous RRM2B missense mutation in association with severe mtDNA depletion.

Kollberg G, Darin N, Benan K, Moslemi AR, Lindal S, Tulinius M, Oldfors A, Holme E. Kollberg G, et al. Among authors: holme e. Neuromuscul Disord. 2009 Feb;19(2):147-50. doi: 10.1016/j.nmd.2008.11.014. Epub 2009 Jan 12. Neuromuscul Disord. 2009. PMID: 19138848

8

A family with pyruvate dehydrogenase complex deficiency due to a novel C>T substitution at nucleotide position 407 in exon 4 of the X-linked Epsilon1alpha gene.

Tulinius M, Darin N, Wiklund LM, Holmberg E, Eriksson JE, Lissens W, De Meirleir L, Holme E. Tulinius M, et al. Among authors: holme e. Eur J Pediatr. 2005 Feb;164(2):99-103. doi: 10.1007/s00431-004-1570-2. Epub 2004 Nov 19. Eur J Pediatr. 2005. PMID: 15558317

9

Atypical presentation of multisystem disorders in two girls with mitochondrial DNA deletions.

Tulinius MH, Oldfors A, Holme E, Larsson NG, Houshmand M, Fahleson P, Sigström L, Kristiansson B. Tulinius MH, et al. Among authors: holme e. Eur J Pediatr. 1995 Jan;154(1):35-42. doi: 10.1007/BF01972970. Eur J Pediatr. 1995. PMID: 7895754

10

Low levels of mitochondrial transcription factor A in mitochondrial DNA depletion.

Larsson NG, Oldfors A, Holme E, Clayton DA. Larsson NG, et al. Among authors: holme e. Biochem Biophys Res Commun. 1994 May 16;200(3):1374-81. doi: 10.1006/bbrc.1994.1603. Biochem Biophys Res Commun. 1994. PMID: 8185589

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