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P Seibel

Showing results (31-40 of 49) with videos related to

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Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|January 1, 1996
Islet cell antibodies in diabetes mellitus associated with a mitochondrial tRNA(Leu(UUR)) gene mutationK Oexle, J Oberle, B Finckh, et al.
Neurology|May 29, 2001
Cricopharyngeal achalasia is a common cause of dysphagia in patients with mtDNA deletionsC Kornblum, R Broicher, E Walther, et al.
Pediatric Research|November 1, 1990
Mitochondrial DNA mutations associated with neuromuscular diseases: analysis and diagnosis using the polymerase chain reactionD C Wallace, M T Lott, A M Lezza, et al.
Human Pathology|December 1, 1992
In situ hybridization of mitochondrial DNA in the heart of a patient with Kearns-Sayre syndrome and dilatative cardiomyopathyJ Müller-Höcker, P Seibel, K Schneiderbanger, et al.
European Neurology|February 26, 1998
Follow-up in carriers of the 'MELAS' mutation without strokesM S Damian, A Hertel, P Seibel, et al.
Cell|June 15, 1990
Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutationJ M Shoffner, M T Lott, A M Lezza, et al.
Acta Neurologica Scandinavica|November 1, 1995
Clinical spectrum of the MELAS mutation in a large pedigreeM S Damian, P Seibel, H Reichmann, et al.
Biological Chemistry|September 24, 1999
Processing of artificial peptide-DNA-conjugates by the mitochondrial intermediate peptidase (MIP)M Seibel, C Bachmann, J Schmiedel, et al.
Journal of Neurology|July 1, 1995
Lipoic (thioctic) acid increases brain energy availability and skeletal muscle performance as shown by in vivo 31P-MRS in a patient with mitochondrial cytopathyB Barbiroli, R Medori, H J Tritschler, et al.
Human Pathology|June 1, 1996
Defects of the respiratory chain in oxyphil and chief cells of the normal parathyroid and in hyperfunctionJ Müller-Höcker, D Aust, J Napiwotzky, et al.
Pageof 5

Showing results (31-40 of 49) with videos related to

Sort By:
Pageof 5
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|January 1, 1996
Islet cell antibodies in diabetes mellitus associated with a mitochondrial tRNA(Leu(UUR)) gene mutationK Oexle, J Oberle, B Finckh, et al.
Neurology|May 29, 2001
Cricopharyngeal achalasia is a common cause of dysphagia in patients with mtDNA deletionsC Kornblum, R Broicher, E Walther, et al.
Pediatric Research|November 1, 1990
Mitochondrial DNA mutations associated with neuromuscular diseases: analysis and diagnosis using the polymerase chain reactionD C Wallace, M T Lott, A M Lezza, et al.
Human Pathology|December 1, 1992
In situ hybridization of mitochondrial DNA in the heart of a patient with Kearns-Sayre syndrome and dilatative cardiomyopathyJ Müller-Höcker, P Seibel, K Schneiderbanger, et al.
European Neurology|February 26, 1998
Follow-up in carriers of the 'MELAS' mutation without strokesM S Damian, A Hertel, P Seibel, et al.
Cell|June 15, 1990
Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutationJ M Shoffner, M T Lott, A M Lezza, et al.
Acta Neurologica Scandinavica|November 1, 1995
Clinical spectrum of the MELAS mutation in a large pedigreeM S Damian, P Seibel, H Reichmann, et al.
Biological Chemistry|September 24, 1999
Processing of artificial peptide-DNA-conjugates by the mitochondrial intermediate peptidase (MIP)M Seibel, C Bachmann, J Schmiedel, et al.
Journal of Neurology|July 1, 1995
Lipoic (thioctic) acid increases brain energy availability and skeletal muscle performance as shown by in vivo 31P-MRS in a patient with mitochondrial cytopathyB Barbiroli, R Medori, H J Tritschler, et al.
Human Pathology|June 1, 1996
Defects of the respiratory chain in oxyphil and chief cells of the normal parathyroid and in hyperfunctionJ Müller-Höcker, D Aust, J Napiwotzky, et al.
Pageof 5