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Clinical spectrum of the MELAS mutation in a large pedigree.
Damian MS, Seibel P, Reichmann H, Schachenmayr W, Laube H, Bachmann G, Wassill KH, Dorndorf W. Damian MS, et al. Among authors: seibel p. Acta Neurol Scand. 1995 Nov;92(5):409-15. doi: 10.1111/j.1600-0404.1995.tb00156.x. Acta Neurol Scand. 1995. PMID: 8610496
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
Follow-up in carriers of the 'MELAS' mutation without strokes.
Damian MS, Hertel A, Seibel P, Reichmann H, Bachmann G, Schachenmayr W, Hoer G, Dorndorf W. Damian MS, et al. Among authors: seibel p. Eur Neurol. 1998;39(1):9-15. doi: 10.1159/000007892. Eur Neurol. 1998. PMID: 9476718 Clinical Trial.
Expression pattern of mitochondrial respiratory chain enzymes in skeletal muscle of patients harboring the A3243G point mutation or large-scale deletions of mitochondrial DNA.
Vielhaber S, Varlamov DA, Kudina TA, Schröder R, Kappes-Horn K, Elger CE, Seibel M, Seibel P, Kunz WS. Vielhaber S, et al. Among authors: seibel m, seibel p. J Neuropathol Exp Neurol. 2002 Oct;61(10):885-95. doi: 10.1093/jnen/61.10.885. J Neuropathol Exp Neurol. 2002. PMID: 12387454
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.
VACTERL with the mitochondrial np 3243 point mutation.
Damian MS, Seibel P, Schachenmayr W, Reichmann H, Dorndorf W. Damian MS, et al. Among authors: seibel p. Am J Med Genet. 1996 Apr 24;62(4):398-403. doi: 10.1002/(SICI)1096-8628(19960424)62:4<398::AID-AJMG13>3.0.CO;2-J. Am J Med Genet. 1996. PMID: 8723071
93 results