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K D Gerbitz

Showing results (31-40 of 63) with videos related to

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Journal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|December 1, 1986
Enolase isoenzymes as tumour markersK D Gerbitz, J Summer, I Schumacher, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|September 1, 1989
Characterization and localization of basement membrane-associated heparan sulfate proteoglycan in human tissuesE D Schleicher, E M Wagner, B Olgemöller, 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.
European Journal of Clinical Investigation|December 1, 1979
Free insulin, bound insulin, C-peptide and the metabolic control in juvenile onset diabetics: comparison of C-peptide secretors and non-secretors during 24 hours conventional insulin therapyK D Gerbitz, W Kemmler, A Edelmann, 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.
Muscle & Nerve. Supplement|January 1, 1995
Maternally inherited diabetes and deafness (MIDD): a distinct subtype of diabetes associated with a mitochondrial tRNA(Leu)(UUR) gene point mutationJ M van den Ouweland, H H Lemkes, K D Gerbitz, 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 Neurology|February 1, 1990
Mitochondrial myopathies: divergences of genetic deletions, biochemical defects and the clinical syndromesK D Gerbitz, B Obermaier-Kusser, S Zierz, et al.
Biochemical and Biophysical Research Communications|July 30, 1999
Carnitine transporter OCTN2 mutations in systemic primary carnitine deficiency: a novel Arg169Gln mutation and a recurrent Arg282ter mutation associated with an unconventional splicing abnormalityB Burwinkel, J Kreuder, S Schweitzer, et al.
European Journal of Pediatrics|October 5, 2001
"Adult" form of muscular carnitine palmitoyltransferase II deficiency: manifestation in a 2-year-old childK Gempel, C von Praun, J Baumkötter, et al.
Pageof 7

Showing results (31-40 of 63) with videos related to

Sort By:
Pageof 7
Journal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|December 1, 1986
Enolase isoenzymes as tumour markersK D Gerbitz, J Summer, I Schumacher, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|September 1, 1989
Characterization and localization of basement membrane-associated heparan sulfate proteoglycan in human tissuesE D Schleicher, E M Wagner, B Olgemöller, 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.
European Journal of Clinical Investigation|December 1, 1979
Free insulin, bound insulin, C-peptide and the metabolic control in juvenile onset diabetics: comparison of C-peptide secretors and non-secretors during 24 hours conventional insulin therapyK D Gerbitz, W Kemmler, A Edelmann, 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.
Muscle & Nerve. Supplement|January 1, 1995
Maternally inherited diabetes and deafness (MIDD): a distinct subtype of diabetes associated with a mitochondrial tRNA(Leu)(UUR) gene point mutationJ M van den Ouweland, H H Lemkes, K D Gerbitz, 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 Neurology|February 1, 1990
Mitochondrial myopathies: divergences of genetic deletions, biochemical defects and the clinical syndromesK D Gerbitz, B Obermaier-Kusser, S Zierz, et al.
Biochemical and Biophysical Research Communications|July 30, 1999
Carnitine transporter OCTN2 mutations in systemic primary carnitine deficiency: a novel Arg169Gln mutation and a recurrent Arg282ter mutation associated with an unconventional splicing abnormalityB Burwinkel, J Kreuder, S Schweitzer, et al.
European Journal of Pediatrics|October 5, 2001
"Adult" form of muscular carnitine palmitoyltransferase II deficiency: manifestation in a 2-year-old childK Gempel, C von Praun, J Baumkötter, et al.
Pageof 7