Kottlors M - Search Results

1

A rapid and sensitive PCR screening method for point mutations associated with mitochondrial encephalomyopathies.

Seibel P, Flierl A, Kottlors M, Reichmann H. Seibel P, et al. Among authors: kottlors m. Biochem Biophys Res Commun. 1994 Apr 29;200(2):938-42. doi: 10.1006/bbrc.1994.1540. Biochem Biophys Res Commun. 1994. PMID: 8179630

2

Multiple symmetric lipomatosis: abnormalities in complex IV and multiple deletions in mitochondrial DNA.

Klopstock T, Naumann M, Schalke B, Bischof F, Seibel P, Kottlors M, Eckert P, Reiners K, Toyka KV, Reichmann H. Klopstock T, et al. Among authors: kottlors m. Neurology. 1994 May;44(5):862-6. doi: 10.1212/wnl.44.5.862. Neurology. 1994. PMID: 8190288

3

Valproic acid triggers acute rhabdomyolysis in a patient with carnitine palmitoyltransferase type II deficiency.

Kottlors M, Jaksch M, Ketelsen UP, Weiner S, Glocker FX, Lücking CH. Kottlors M, et al. Neuromuscul Disord. 2001 Nov;11(8):757-9. doi: 10.1016/s0960-8966(01)00228-0. Neuromuscul Disord. 2001. PMID: 11595519

4

Adult carnitine palmitoyltransferase II deficiency: detection of characteristic carnitine esters in serum by tandem mass spectrometry.

Gempel K, Kottlors M, Jaksch M, Gerbitz KD, Bauer MF. Gempel K, et al. Among authors: kottlors m. J Inherit Metab Dis. 1999 Dec;22(8):941-2. doi: 10.1023/a:1005655927639. J Inherit Metab Dis. 1999. PMID: 10604150 No abstract available.

5

Polysegmental innervation of the medial paraspinal lumbar muscles.

Kottlors M, Glocker FX. Kottlors M, et al. Eur Spine J. 2008 Feb;17(2):300-6. doi: 10.1007/s00586-007-0529-1. Epub 2007 Oct 31. Eur Spine J. 2008. PMID: 17972114 Free PMC article.

6

Facioscapulohumeral muscular dystrophy presenting with isolated axial myopathy and bent spine syndrome.

Kottlors M, Kress W, Meng G, Glocker FX. Kottlors M, et al. Muscle Nerve. 2010 Aug;42(2):273-5. doi: 10.1002/mus.21722. Muscle Nerve. 2010. PMID: 20658601

7

Muscle hypertrophy of the lower leg caused by L5 radiculopathy.

Kottlors M, Mueller K, Kirschner J, Glocker FX. Kottlors M, et al. Joint Bone Spine. 2009 Oct;76(5):562-4. doi: 10.1016/j.jbspin.2009.01.009. Epub 2009 Jun 11. Joint Bone Spine. 2009. PMID: 19523866

8

Dermatomyotomal supply in patients with variations in the number of lumbar vertebrae.

Kottlors M, Glocker FX. Kottlors M, et al. J Neurosurg Spine. 2010 Mar;12(3):314-9. doi: 10.3171/2009.9.SPINE09114. J Neurosurg Spine. 2010. PMID: 20192633

9

Late-onset autosomal dominant limb girdle muscular dystrophy and Paget's disease of bone unlinked to the VCP gene locus.

Kottlors M, Moske-Eick O, Huebner A, Krause S, Mueller K, Kress W, Schwarzwald R, Bornemann A, Haug V, Heitzer M, Kirschner J. Kottlors M, et al. J Neurol Sci. 2010 Apr 15;291(1-2):79-85. doi: 10.1016/j.jns.2009.12.008. Epub 2010 Feb 8. J Neurol Sci. 2010. PMID: 20116073

10

Elevated satellite cell number in Duchenne muscular dystrophy.

Kottlors M, Kirschner J. Kottlors M, et al. Cell Tissue Res. 2010 Jun;340(3):541-8. doi: 10.1007/s00441-010-0976-6. Epub 2010 May 15. Cell Tissue Res. 2010. PMID: 20467789

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