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Mitochondrial cytopathies.
Schmiedel J, Jackson S, Schäfer J, Reichmann H. Schmiedel J, et al. Among authors: reichmann h. J Neurol. 2003 Mar;250(3):267-77. doi: 10.1007/s00415-003-0978-3. J Neurol. 2003. PMID: 12638015 Review.
[Mitochondrial diseases].
Schaefer J, Reichmann H. Schaefer J, et al. Among authors: reichmann h. Dtsch Med Wochenschr. 2001 Aug 17;126(33):913-7. doi: 10.1055/s-2001-16497. Dtsch Med Wochenschr. 2001. PMID: 11514927 Review. German. No abstract available.
Subcutaneous microdialysis in mitochondrial cytopathy.
Damian MS, Sauter W, Reichmann H. Damian MS, et al. Among authors: reichmann h. Muscle Nerve. 2001 May;24(5):648-53. doi: 10.1002/mus.1050. Muscle Nerve. 2001. PMID: 11317274 Clinical Trial.
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: reichmann h. Acta Neurol Scand. 1995 Nov;92(5):409-15. doi: 10.1111/j.1600-0404.1995.tb00156.x. Acta Neurol Scand. 1995. PMID: 8610496
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: reichmann h. Eur Neurol. 1998;39(1):9-15. doi: 10.1159/000007892. Eur Neurol. 1998. PMID: 9476718 Clinical Trial.
VACTERL with the mitochondrial np 3243 point mutation.
Damian MS, Seibel P, Schachenmayr W, Reichmann H, Dorndorf W. Damian MS, et al. Among authors: reichmann h. 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
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