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H H Seydewitz

Showing results (1-10 of 21) with videos related to

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Human Mutation|December 29, 1999
Molecular genetic analysis of 40 patients with glycogen storage disease type Ia: 100% mutation detection rate and 5 novel mutationsH H Seydewitz, D Matern
Thrombosis Research|October 1, 1985
Increased phosphorylation of human fibrinopeptide A under acute phase conditionsH H Seydewitz, I Witt
Clinical Chemistry and Laboratory Medicine|January 5, 2002
Pediatric reference ranges for osteocalcin measured by the Immulite analyzerH H Seydewitz, M Henschen, W Kühnel, et al.
Thrombosis Research|March 1, 1984
The location of a second in vivo phosphorylation site in the A alpha-chain of human fibrinogenH H Seydewitz, C Kaiser, H Rothweiler, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 1, 1991
Fibrinogen Kiel: a congenital dysfibrinogenaemia with (A alpha-16 Arg----His) substitution characterized by HPLC without prior isolation of fibrinogenH H Seydewitz, J Gram, H D Bruhn, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 1, 1994
A novel homozygous missense mutation (Val 325-->Ala) in the protein C gene causing neonatal purpura fulminansI Witt, S Beck, H H Seydewitz, et al.
Thrombosis Research|May 1, 1987
Increase in the degree of phosphorylation of circulating fibrinogen under thrombolytic therapy with urokinaseH H Seydewitz, F R Matthias, T H Schöndorf, et al.
Biochimica Et Biophysica Acta|November 29, 1985
Characterisation of calmodulin from Drosophila headsM Görlach, P Dieter, H H Seydewitz, et al.
European Journal of Pediatrics|December 1, 1983
Hereditary hypofibrinogenemia with fibrinogen storage in the liverH Wehinger, O Klinge, E Alexandrakis, et al.
European Journal of Biochemistry|January 2, 1984
Isolation and complete amino-acid sequence of the small polypeptide from light-harvesting pigment-protein complex I (B870) of Rhodopseudomonas capsulataM H Tadros, F Suter, H H Seydewitz, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Human Mutation|December 29, 1999
Molecular genetic analysis of 40 patients with glycogen storage disease type Ia: 100% mutation detection rate and 5 novel mutationsH H Seydewitz, D Matern
Thrombosis Research|October 1, 1985
Increased phosphorylation of human fibrinopeptide A under acute phase conditionsH H Seydewitz, I Witt
Clinical Chemistry and Laboratory Medicine|January 5, 2002
Pediatric reference ranges for osteocalcin measured by the Immulite analyzerH H Seydewitz, M Henschen, W Kühnel, et al.
Thrombosis Research|March 1, 1984
The location of a second in vivo phosphorylation site in the A alpha-chain of human fibrinogenH H Seydewitz, C Kaiser, H Rothweiler, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 1, 1991
Fibrinogen Kiel: a congenital dysfibrinogenaemia with (A alpha-16 Arg----His) substitution characterized by HPLC without prior isolation of fibrinogenH H Seydewitz, J Gram, H D Bruhn, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 1, 1994
A novel homozygous missense mutation (Val 325-->Ala) in the protein C gene causing neonatal purpura fulminansI Witt, S Beck, H H Seydewitz, et al.
Thrombosis Research|May 1, 1987
Increase in the degree of phosphorylation of circulating fibrinogen under thrombolytic therapy with urokinaseH H Seydewitz, F R Matthias, T H Schöndorf, et al.
Biochimica Et Biophysica Acta|November 29, 1985
Characterisation of calmodulin from Drosophila headsM Görlach, P Dieter, H H Seydewitz, et al.
European Journal of Pediatrics|December 1, 1983
Hereditary hypofibrinogenemia with fibrinogen storage in the liverH Wehinger, O Klinge, E Alexandrakis, et al.
European Journal of Biochemistry|January 2, 1984
Isolation and complete amino-acid sequence of the small polypeptide from light-harvesting pigment-protein complex I (B870) of Rhodopseudomonas capsulataM H Tadros, F Suter, H H Seydewitz, et al.
Pageof 3