Kottlors M - Search Results

1

Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS.

Kim HJ, Kim NC, Wang YD, Scarborough EA, Moore J, Diaz Z, MacLea KS, Freibaum B, Li S, Molliex A, Kanagaraj AP, Carter R, Boylan KB, Wojtas AM, Rademakers R, Pinkus JL, Greenberg SA, Trojanowski JQ, Traynor BJ, Smith BN, Topp S, Gkazi AS, Miller J, Shaw CE, Kottlors M, Kirschner J, Pestronk A, Li YR, Ford AF, Gitler AD, Benatar M, King OD, Kimonis VE, Ross ED, Weihl CC, Shorter J, Taylor JP. Kim HJ, et al. Among authors: kottlors m. Nature. 2013 Mar 28;495(7442):467-73. doi: 10.1038/nature11922. Epub 2013 Mar 3. Nature. 2013. PMID: 23455423 Free PMC article.

2

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

3

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

4

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

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

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

7

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

8

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

9

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.

10

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

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