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I Witt

Showing results (61-70 of 106) with videos related to

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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.
Neurologic Clinics|August 1, 1990
Rett syndrome and the autistic disordersA Percy, C Gillberg, B Hagberg, et al.
Biochemical and Biophysical Research Communications|December 28, 1979
Amino acid sequence of yeast proteinase B inhibitor 1 comparison with inhibitor 2K Maier, H Müller, R Tesch, et al.
Monatsschrift Fur Kinderheilkunde|May 1, 1977
[Isovaleric acidemia in a small infant]H Niederhoff, W Lehnert, I Witt, et al.
Helvetica Paediatrica Acta|September 1, 1972
Multiple exchange transfusions as treatment during the acute period in maple syrup urine diseaseL Schuchmann, I Witt, P Schulz, et al.
Stroke|July 1, 1990
Ischemic stroke due to protein C deficiencyJ Kohler, J Kasper, I Witt, et al.
Klinische Wochenschrift|September 15, 1982
Renal metabolism of corticosteroid hormonesK Hierholzer, I Lichtenstein, H Siebe, et al.
Hamostaseologie|August 24, 2002
[Fibrinogen variation: a heterozygote dysfibrinogenemia with Arg-->His substitution in position 16 of the Aalpha chain]H H Seydewitz, J Gram, H D Bruhn, et al.
Klinische Wochenschrift|December 15, 1981
Decreased production or increased turnover of antithrombin III in severe acquired coagulopathy?B Schmidt, U Wais, W Pringsheim, 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.
Pageof 11

Showing results (61-70 of 106) with videos related to

Sort By:
Pageof 11
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.
Neurologic Clinics|August 1, 1990
Rett syndrome and the autistic disordersA Percy, C Gillberg, B Hagberg, et al.
Biochemical and Biophysical Research Communications|December 28, 1979
Amino acid sequence of yeast proteinase B inhibitor 1 comparison with inhibitor 2K Maier, H Müller, R Tesch, et al.
Monatsschrift Fur Kinderheilkunde|May 1, 1977
[Isovaleric acidemia in a small infant]H Niederhoff, W Lehnert, I Witt, et al.
Helvetica Paediatrica Acta|September 1, 1972
Multiple exchange transfusions as treatment during the acute period in maple syrup urine diseaseL Schuchmann, I Witt, P Schulz, et al.
Stroke|July 1, 1990
Ischemic stroke due to protein C deficiencyJ Kohler, J Kasper, I Witt, et al.
Klinische Wochenschrift|September 15, 1982
Renal metabolism of corticosteroid hormonesK Hierholzer, I Lichtenstein, H Siebe, et al.
Hamostaseologie|August 24, 2002
[Fibrinogen variation: a heterozygote dysfibrinogenemia with Arg-->His substitution in position 16 of the Aalpha chain]H H Seydewitz, J Gram, H D Bruhn, et al.
Klinische Wochenschrift|December 15, 1981
Decreased production or increased turnover of antithrombin III in severe acquired coagulopathy?B Schmidt, U Wais, W Pringsheim, 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.
Pageof 11