Seibel P - Search Results

1

Progression of myopathology in Kearns-Sayre syndrome: a morphological follow-up study.

Reichmann H, Gold R, Meurers B, Naumann M, Seibel P, Walter U, Klopstock T. Reichmann H, et al. Among authors: seibel p. Acta Neuropathol. 1993;85(6):679-81. doi: 10.1007/BF00334681. Acta Neuropathol. 1993. PMID: 8393264

2

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: seibel p. Acta Neuropathol. 1995;90(2):126-9. doi: 10.1007/BF00294310. Acta Neuropathol. 1995. PMID: 7484086

3

Sarcoid myopathy and mitochondrial respiratory chain defects: clinicopathological, biochemical and molecular biological analyses.

Reichmann H, Schalke B, Seibel P, Naumann M, Toyka K. Reichmann H, et al. Among authors: seibel p. Neuromuscul Disord. 1995 Jul;5(4):277-83. doi: 10.1016/0960-8966(94)00060-m. Neuromuscul Disord. 1995. PMID: 7580239

4

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: seibel p. Neurology. 1994 May;44(5):862-6. doi: 10.1212/wnl.44.5.862. Neurology. 1994. PMID: 8190288

5

Mitochondrial DNA in migraine with aura.

Klopstock T, May A, Seibel P, Papagiannuli E, Diener HC, Reichmann H. Klopstock T, et al. Among authors: seibel p. Neurology. 1996 Jun;46(6):1735-8. doi: 10.1212/wnl.46.6.1735. Neurology. 1996. PMID: 8649580

6

Ragged red or ragged blue fibers.

Reichmann H, Vogler L, Seibel P. Reichmann H, et al. Among authors: seibel p. Eur Neurol. 1996;36(2):98-102. doi: 10.1159/000117217. Eur Neurol. 1996. PMID: 8654494

7

Mitochondrial dysfunction with myoclonus epilepsy and ragged-red fibers point mutation in nerve, muscle, and adipose tissue of a patient with multiple symmetric lipomatosis.

Naumann M, Kiefer R, Toyka KV, Sommer C, Seibel P, Reichmann H. Naumann M, et al. Among authors: seibel p. Muscle Nerve. 1997 Jul;20(7):833-9. doi: 10.1002/(sici)1097-4598(199707)20:7<833::aid-mus7>3.0.co;2-8. Muscle Nerve. 1997. PMID: 9179155

8

Mitochondrial DNA mutations in multiple symmetric lipomatosis.

Klopstock T, Naumann M, Seibel P, Shalke B, Reiners K, Reichmann H. Klopstock T, et al. Among authors: seibel p. Mol Cell Biochem. 1997 Sep;174(1-2):271-5. Mol Cell Biochem. 1997. PMID: 9309699

9

New insights into the metabolic consequences of large-scale mtDNA deletions: a quantitative analysis of biochemical, morphological, and genetic findings in human skeletal muscle.

Schröder R, Vielhaber S, Wiedemann FR, Kornblum C, Papassotiropoulos A, Broich P, Zierz S, Elger CE, Reichmann H, Seibel P, Klockgether T, Kunz WS. Schröder R, et al. Among authors: seibel p. J Neuropathol Exp Neurol. 2000 May;59(5):353-60. doi: 10.1093/jnen/59.5.353. J Neuropathol Exp Neurol. 2000. PMID: 10888364

10

Pathophysiology of the MELAS 3243 transition mutation.

Flierl A, Reichmann H, Seibel P. Flierl A, et al. Among authors: seibel p. J Biol Chem. 1997 Oct 24;272(43):27189-96. doi: 10.1074/jbc.272.43.27189. J Biol Chem. 1997. PMID: 9341162 Free article.

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