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K Widhalm

Showing results (111-120 of 225) with videos related to

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Klinische Padiatrie|September 1, 1976
[Combination of the syndrome of Sturge-Weber and the syndrome of Klippel-Trénaunay (author's transl)]J Deutsch, G Weissenbacher, K Widhalm, et al.
Acta Paediatrica Scandinavica|July 1, 1980
Glycosylated hemoglobin (HbAtc) and plasma lipoproteins in juvenile onset diabetes mellitusA Pollak, K Widhalm, L Havelec, et al.
Kidney International. Supplement|December 1, 1983
Lipid metabolism in acute renal failureW Druml, A Laggner, K Widhalm, et al.
Journal of the American College of Nutrition|June 1, 1992
Serum lipids, lipoproteins and apolipoproteins in children with and without familial history of premature coronary heart diseaseK Widhalm, S Koch, R Pakosta, et al.
Applied Pathology|January 1, 1986
Platelet plasma membrane changes in human type IIa hypercholesterolemiaG Bianciardi, G Weber, P Toti, et al.
International Journal of Cardiology|January 1, 1987
Potential life-threatening cardiac arrhythmias associated with a conventional hypocaloric dietH Schmidinger, H Weber, K Zwiauer, et al.
Helvetica Paediatrica Acta|May 1, 1984
[Diagnosis and effective therapy with plasmapheresis in a patient with homozygous familial hypercholesterolemia]K Widhalm, G Kleinberger, W Strobl, et al.
Prostaglandins and Medicine|August 1, 1981
Value of platelet sensitivity to antiaggregatory prostaglandins (PGI2, PGE1, PGD2) in 50 patients with myocardial infarction at young ageH Sinzinger, J Kaliman, K Widhalm, et al.
Wiener Klinische Wochenschrift|September 3, 1982
[Platelet half-life in patients with primary hyperlipoproteinemia type IIa, IIb, and IV according to Fredrickson with and without clinical signs of atherosclerosis]E Jäger, H Sinzinger, K Widhalm, et al.
Human Mutation|September 30, 1999
Heterozygous familial hypercholesterolemia: a new point-mutation (1372del2) in the LDL-receptor gene which causes severe hypercholesterolemiaK Widhalm, C Iro, A Lindemayr, et al.
Pageof 23

Showing results (111-120 of 225) with videos related to

Sort By:
Pageof 23
Klinische Padiatrie|September 1, 1976
[Combination of the syndrome of Sturge-Weber and the syndrome of Klippel-Trénaunay (author's transl)]J Deutsch, G Weissenbacher, K Widhalm, et al.
Acta Paediatrica Scandinavica|July 1, 1980
Glycosylated hemoglobin (HbAtc) and plasma lipoproteins in juvenile onset diabetes mellitusA Pollak, K Widhalm, L Havelec, et al.
Kidney International. Supplement|December 1, 1983
Lipid metabolism in acute renal failureW Druml, A Laggner, K Widhalm, et al.
Journal of the American College of Nutrition|June 1, 1992
Serum lipids, lipoproteins and apolipoproteins in children with and without familial history of premature coronary heart diseaseK Widhalm, S Koch, R Pakosta, et al.
Applied Pathology|January 1, 1986
Platelet plasma membrane changes in human type IIa hypercholesterolemiaG Bianciardi, G Weber, P Toti, et al.
International Journal of Cardiology|January 1, 1987
Potential life-threatening cardiac arrhythmias associated with a conventional hypocaloric dietH Schmidinger, H Weber, K Zwiauer, et al.
Helvetica Paediatrica Acta|May 1, 1984
[Diagnosis and effective therapy with plasmapheresis in a patient with homozygous familial hypercholesterolemia]K Widhalm, G Kleinberger, W Strobl, et al.
Prostaglandins and Medicine|August 1, 1981
Value of platelet sensitivity to antiaggregatory prostaglandins (PGI2, PGE1, PGD2) in 50 patients with myocardial infarction at young ageH Sinzinger, J Kaliman, K Widhalm, et al.
Wiener Klinische Wochenschrift|September 3, 1982
[Platelet half-life in patients with primary hyperlipoproteinemia type IIa, IIb, and IV according to Fredrickson with and without clinical signs of atherosclerosis]E Jäger, H Sinzinger, K Widhalm, et al.
Human Mutation|September 30, 1999
Heterozygous familial hypercholesterolemia: a new point-mutation (1372del2) in the LDL-receptor gene which causes severe hypercholesterolemiaK Widhalm, C Iro, A Lindemayr, et al.
Pageof 23