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M Jaksch

Showing results (11-20 of 38) with videos related to

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Biochimica Et Biophysica Acta|May 24, 1995
Mitochondrial diabetes mellitus: a reviewK D Gerbitz, J M van den Ouweland, J A Maassen, et al.
Gut|June 14, 2005
Identification of expandable human hepatic progenitors which differentiate into mature hepatic cells in vivoG Nowak, B-G Ericzon, S Nava, et al.
Clinical Chemistry and Laboratory Medicine|December 22, 1999
Mitochondrial disorders. A diagnostic challenge in clinical chemistryM F Bauer, K Gempel, S Hofmann, et al.
Molecular and Cellular Biochemistry|October 6, 1997
Analysis of the mitochondrial DNA from patients with Wolfram (DIDMOAD) syndromeS Hofmann, R Bezold, M Jaksch, et al.
Neuromuscular Disorders : NMD|November 18, 2005
Mutations in mtDNA-encoded cytochrome c oxidase subunit genes causing isolated myopathy or severe encephalomyopathyR Horváth, B G H Schoser, J Müller-Höcker, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 17, 1999
Different clinical aspects of debrancher deficiency myopathyS Kiechl, U Kohlendorfer, C Thaler, et al.
Neuromuscular Disorders : NMD|October 12, 2001
Valproic acid triggers acute rhabdomyolysis in a patient with carnitine palmitoyltransferase type II deficiencyM Kottlors, M Jaksch, U P Ketelsen, et al.
Human Molecular Genetics|September 25, 1997
Population genetics and disease susceptibility: characterization of central European haplogroups by mtDNA gene mutations, correlation with D loop variants and association with diseaseS Hofmann, M Jaksch, R Bezold, et al.
Journal of Medical Genetics|September 9, 2000
A novel mutation in the thiamine responsive megaloblastic anaemia gene SLC19A2 in a patient with deficiency of respiratory chain complex IC Scharfe, M Hauschild, T Klopstock, et al.
Human Molecular Genetics|April 6, 2000
Mutations in SCO2 are associated with a distinct form of hypertrophic cardiomyopathy and cytochrome c oxidase deficiencyM Jaksch, I Ogilvie, J Yao, et al.
Pageof 4

Showing results (11-20 of 38) with videos related to

Sort By:
Pageof 4
Biochimica Et Biophysica Acta|May 24, 1995
Mitochondrial diabetes mellitus: a reviewK D Gerbitz, J M van den Ouweland, J A Maassen, et al.
Gut|June 14, 2005
Identification of expandable human hepatic progenitors which differentiate into mature hepatic cells in vivoG Nowak, B-G Ericzon, S Nava, et al.
Clinical Chemistry and Laboratory Medicine|December 22, 1999
Mitochondrial disorders. A diagnostic challenge in clinical chemistryM F Bauer, K Gempel, S Hofmann, et al.
Molecular and Cellular Biochemistry|October 6, 1997
Analysis of the mitochondrial DNA from patients with Wolfram (DIDMOAD) syndromeS Hofmann, R Bezold, M Jaksch, et al.
Neuromuscular Disorders : NMD|November 18, 2005
Mutations in mtDNA-encoded cytochrome c oxidase subunit genes causing isolated myopathy or severe encephalomyopathyR Horváth, B G H Schoser, J Müller-Höcker, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 17, 1999
Different clinical aspects of debrancher deficiency myopathyS Kiechl, U Kohlendorfer, C Thaler, et al.
Neuromuscular Disorders : NMD|October 12, 2001
Valproic acid triggers acute rhabdomyolysis in a patient with carnitine palmitoyltransferase type II deficiencyM Kottlors, M Jaksch, U P Ketelsen, et al.
Human Molecular Genetics|September 25, 1997
Population genetics and disease susceptibility: characterization of central European haplogroups by mtDNA gene mutations, correlation with D loop variants and association with diseaseS Hofmann, M Jaksch, R Bezold, et al.
Journal of Medical Genetics|September 9, 2000
A novel mutation in the thiamine responsive megaloblastic anaemia gene SLC19A2 in a patient with deficiency of respiratory chain complex IC Scharfe, M Hauschild, T Klopstock, et al.
Human Molecular Genetics|April 6, 2000
Mutations in SCO2 are associated with a distinct form of hypertrophic cardiomyopathy and cytochrome c oxidase deficiencyM Jaksch, I Ogilvie, J Yao, et al.
Pageof 4