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P Seibel

Showing results (21-30 of 49) with videos related to

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Molecular and Cellular Biochemistry|October 6, 1997
Mitochondrial DNA mutations in multiple symmetric lipomatosisT Klopstock, M Naumann, P Seibel, et al.
Muscle & Nerve|July 1, 1997
Mitochondrial dysfunction with myoclonus epilepsy and ragged-red fibers point mutation in nerve, muscle, and adipose tissue of a patient with multiple symmetric lipomatosisM Naumann, R Kiefer, K V Toyka, et al.
Neurology|June 1, 1996
Mitochondrial DNA in migraine with auraT Klopstock, A May, P Seibel, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|May 3, 2003
Targeted delivery of DNA to the mitochondrial compartment via import sequence-conjugated peptide nucleic acidA Flierl, C Jackson, B Cottrell, et al.
Der Nervenarzt|April 1, 1994
[MELAS syndrome. Clinical aspects, MRI, biochemistry and molecular genetics]M S Damian, H Reichmann, P Seibel, et al.
Acta Neuropathologica|January 1, 1993
Progression of myopathology in Kearns-Sayre syndrome: a morphological follow-up studyH Reichmann, R Gold, B Meurers, et al.
European Neurology|January 1, 1996
Phosphorus magnetic resonance spectroscopy in the evaluation of mitochondrial myopathies: results of a 6-month therapy study with coenzyme QR Gold, P Seibel, G Reinelt, et al.
European Neurology|January 1, 1994
Unaltered respiratory chain enzyme activity and mitochondrial DNA in skeletal muscle from patients with idiopathic Parkinson's syndromeH Reichmann, B Janetzky, F Bischof, et al.
Acta Neuropathologica|January 1, 1995
3.1-kb deletion of mitochondrial DNA in a patient with Kearns-Sayre syndromeT Klopstock, F Bischof, K Gerok, et al.
European Journal of Neurology|November 29, 2013
Neuropsychological status of mitochondrial encephalomyopathiesC J Lang, P Brenner, D Heub, et al.
Pageof 5

Showing results (21-30 of 49) with videos related to

Sort By:
Pageof 5
Molecular and Cellular Biochemistry|October 6, 1997
Mitochondrial DNA mutations in multiple symmetric lipomatosisT Klopstock, M Naumann, P Seibel, et al.
Muscle & Nerve|July 1, 1997
Mitochondrial dysfunction with myoclonus epilepsy and ragged-red fibers point mutation in nerve, muscle, and adipose tissue of a patient with multiple symmetric lipomatosisM Naumann, R Kiefer, K V Toyka, et al.
Neurology|June 1, 1996
Mitochondrial DNA in migraine with auraT Klopstock, A May, P Seibel, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|May 3, 2003
Targeted delivery of DNA to the mitochondrial compartment via import sequence-conjugated peptide nucleic acidA Flierl, C Jackson, B Cottrell, et al.
Der Nervenarzt|April 1, 1994
[MELAS syndrome. Clinical aspects, MRI, biochemistry and molecular genetics]M S Damian, H Reichmann, P Seibel, et al.
Acta Neuropathologica|January 1, 1993
Progression of myopathology in Kearns-Sayre syndrome: a morphological follow-up studyH Reichmann, R Gold, B Meurers, et al.
European Neurology|January 1, 1996
Phosphorus magnetic resonance spectroscopy in the evaluation of mitochondrial myopathies: results of a 6-month therapy study with coenzyme QR Gold, P Seibel, G Reinelt, et al.
European Neurology|January 1, 1994
Unaltered respiratory chain enzyme activity and mitochondrial DNA in skeletal muscle from patients with idiopathic Parkinson's syndromeH Reichmann, B Janetzky, F Bischof, et al.
Acta Neuropathologica|January 1, 1995
3.1-kb deletion of mitochondrial DNA in a patient with Kearns-Sayre syndromeT Klopstock, F Bischof, K Gerok, et al.
European Journal of Neurology|November 29, 2013
Neuropsychological status of mitochondrial encephalomyopathiesC J Lang, P Brenner, D Heub, et al.
Pageof 5