Ketelsen UP - Search Results

1

Congenital myopathy with arrest of myogenesis prior to formation of myotubes.

Ketelsen UP, Brand-Saberi B, Uhlenberg B, Wagner M, Laberke HG, Omran H. Ketelsen UP, et al. Neuropediatrics. 2005 Aug;36(4):246-51. doi: 10.1055/s-2005-865773. Neuropediatrics. 2005. PMID: 16138248

2

Identification of a novel LAMP2 mutation responsible for X-chromosomal dominant Danon disease.

Horváth J, Ketelsen UP, Geibel-Zehender A, Boehm N, Olbrich H, Korinthenberg R, Omran H. Horváth J, et al. Among authors: ketelsen up. Neuropediatrics. 2003 Jun;34(5):270-3. doi: 10.1055/s-2003-43262. Neuropediatrics. 2003. PMID: 14598234

3

Abundant minute myotubes in a patient who later developed centronuclear myopathy.

Wöckel L, Ketelsen UP, Stötter M, Laule S, Meyermann R, Bornemann A. Wöckel L, et al. Among authors: ketelsen up. Acta Neuropathol. 1998 May;95(5):547-51. doi: 10.1007/s004010050836. Acta Neuropathol. 1998. PMID: 9600602

4

Genotype-phenotype correlations in PCD patients carrying DNAH5 mutations.

Kispert A, Petry M, Olbrich H, Volz A, Ketelsen UP, Horvath J, Melkaoui R, Omran H, Zariwala M, Noone PG, Knowles M. Kispert A, et al. Among authors: ketelsen up. Thorax. 2003 Jun;58(6):552-4. doi: 10.1136/thorax.58.6.552-b. Thorax. 2003. PMID: 12775878 Free PMC article. No abstract available.

5

Long-term observations of patients with infantile spinal muscular atrophy with respiratory distress type 1 (SMARD1).

Rudnik-Schöneborn S, Stolz P, Varon R, Grohmann K, Schächtele M, Ketelsen UP, Stavrou D, Kurz H, Hübner C, Zerres K. Rudnik-Schöneborn S, et al. Among authors: ketelsen up. Neuropediatrics. 2004 Jun;35(3):174-82. doi: 10.1055/s-2004-820994. Neuropediatrics. 2004. PMID: 15248100

6

3.1-kb deletion of mitochondrial DNA in a patient with Kearns-Sayre syndrome.

Klopstock T, Bischof F, Gerok K, Deuschl G, Seibel P, Ketelsen UP, Reichmann H. Klopstock T, et al. Among authors: ketelsen up. Acta Neuropathol. 1995;90(2):126-9. doi: 10.1007/BF00294310. Acta Neuropathol. 1995. PMID: 7484086

7

Histological, enzymatic and mitochondrial DNA studies in patients with Kearns-Sayre syndrome and chronic progressive external ophthalmoplegia.

Reichmann H, Degoul F, Gold R, Meurers B, Ketelsen UP, Hartmann J, Marsac C, Lestienne P. Reichmann H, et al. Among authors: ketelsen up. Eur Neurol. 1991;31(2):108-13. doi: 10.1159/000116656. Eur Neurol. 1991. PMID: 1646110

8

Cytochrome c oxidase deficiency and long-chain acyl coenzyme A dehydrogenase deficiency with Leigh's subacute necrotizing encephalomyelopathy.

Reichmann H, Scheel H, Bier B, Ketelsen UP, Zabransky S. Reichmann H, et al. Among authors: ketelsen up. Ann Neurol. 1992 Jan;31(1):107-9. doi: 10.1002/ana.410310120. Ann Neurol. 1992. PMID: 1311909

9

Foamy myocardial transformation in a child with a disturbed respiratory chain.

Böhles H, Singer H, Ruitenbeek W, Trijbels JM, Sengers RC, Ketelsen UP, Wagner-Thiessen E, Wick H. Böhles H, et al. Among authors: ketelsen up. Eur J Pediatr. 1987 Nov;146(6):582-6. doi: 10.1007/BF02467358. Eur J Pediatr. 1987. PMID: 2828064

10

Dexrazoxane prevents doxorubicin-induced long-term cardiotoxicity and protects myocardial mitochondria from genetic and functional lesions in rats.

Lebrecht D, Geist A, Ketelsen UP, Haberstroh J, Setzer B, Walker UA. Lebrecht D, et al. Among authors: ketelsen up. Br J Pharmacol. 2007 Jul;151(6):771-8. doi: 10.1038/sj.bjp.0707294. Epub 2007 May 21. Br J Pharmacol. 2007. PMID: 17519947 Free PMC article.

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