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J R Schaefer

Showing results (31-40 of 47) with videos related to

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Neuropediatrics|March 1, 2002
A new subtype of a congenital disorder of glycosylation (CDG) with mild clinical manifestationsB Assmann, R Hackler, V Peters, et al.
Deutsche Medizinische Wochenschrift (1946)|October 2, 2012
[Lipid therapy in daily routine]F Sonntag, J R Schaefer, A K Gitt, et al.
Der Nervenarzt|September 24, 2002
[CDG (congenital disorders of glycosylation). Differential hereditary ataxia in adulthood diagnosis]S Bubel, V Peters, C Klein, et al.
Atherosclerosis|June 8, 2011
Identification of a gene variant in the master regulator of lipid metabolism SREBP-1 in a family with a novel form of severe combined hypolipidemiaJorg Kotzka, Birgit Knebel, Onno E Janssen, et al.
Kidney International|February 15, 2007
In vivo turnover study demonstrates diminished clearance of lipoprotein(a) in hemodialysis patientsM E Frischmann, F Kronenberg, E Trenkwalder, et al.
The Journal of Infectious Diseases|July 1, 1987
A one-year study of endemic campylobacteriosis in a midwestern city: association with consumption of raw milkG P Schmid, R E Schaefer, B D Plikaytis, et al.
Journal of Lipid Research|May 11, 1992
In vivo metabolism of a mutant apolipoprotein, apoA-IIowa, associated with hypoalphalipoproteinemia and hereditary systemic amyloidosisD J Rader, R E Gregg, M S Meng, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|February 1, 1997
Homozygous familial defective apolipoprotein B-100. Enhanced removal of apolipoprotein E-containing VLDLs and decreased production of LDLsJ R Schaefer, H Scharnagl, M W Baumstark, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|July 15, 2000
Increased production of HDL ApoA-I in homozygous familial defective ApoB-100J R Schaefer, K Winkler, H Schweer, et al.
The Journal of Clinical Investigation|October 1, 1993
Delayed catabolism of high density lipoprotein apolipoproteins A-I and A-II in human cholesteryl ester transfer protein deficiencyK Ikewaki, D J Rader, T Sakamoto, et al.
Pageof 5

Showing results (31-40 of 47) with videos related to

Sort By:
Pageof 5
Neuropediatrics|March 1, 2002
A new subtype of a congenital disorder of glycosylation (CDG) with mild clinical manifestationsB Assmann, R Hackler, V Peters, et al.
Deutsche Medizinische Wochenschrift (1946)|October 2, 2012
[Lipid therapy in daily routine]F Sonntag, J R Schaefer, A K Gitt, et al.
Der Nervenarzt|September 24, 2002
[CDG (congenital disorders of glycosylation). Differential hereditary ataxia in adulthood diagnosis]S Bubel, V Peters, C Klein, et al.
Atherosclerosis|June 8, 2011
Identification of a gene variant in the master regulator of lipid metabolism SREBP-1 in a family with a novel form of severe combined hypolipidemiaJorg Kotzka, Birgit Knebel, Onno E Janssen, et al.
Kidney International|February 15, 2007
In vivo turnover study demonstrates diminished clearance of lipoprotein(a) in hemodialysis patientsM E Frischmann, F Kronenberg, E Trenkwalder, et al.
The Journal of Infectious Diseases|July 1, 1987
A one-year study of endemic campylobacteriosis in a midwestern city: association with consumption of raw milkG P Schmid, R E Schaefer, B D Plikaytis, et al.
Journal of Lipid Research|May 11, 1992
In vivo metabolism of a mutant apolipoprotein, apoA-IIowa, associated with hypoalphalipoproteinemia and hereditary systemic amyloidosisD J Rader, R E Gregg, M S Meng, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|February 1, 1997
Homozygous familial defective apolipoprotein B-100. Enhanced removal of apolipoprotein E-containing VLDLs and decreased production of LDLsJ R Schaefer, H Scharnagl, M W Baumstark, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|July 15, 2000
Increased production of HDL ApoA-I in homozygous familial defective ApoB-100J R Schaefer, K Winkler, H Schweer, et al.
The Journal of Clinical Investigation|October 1, 1993
Delayed catabolism of high density lipoprotein apolipoproteins A-I and A-II in human cholesteryl ester transfer protein deficiencyK Ikewaki, D J Rader, T Sakamoto, et al.
Pageof 5