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K Auberger

Showing results (1-10 of 19) with videos related to

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Annals of Hematology|March 1, 1992
Evaluation of a new protein-C concentrate and comparison of protein-C assays in a child with congenital protein-C deficiencyK Auberger
European Journal of Pediatrics|May 2, 2000
Thrombosis of the deep cerebral veins with excessive bilateral infarction in a premature infant with the thrombogenic 4G/4G genotype of the plasminogen activator inhibitor-1F A Baumeister, K Auberger, K Schneider
European Journal of Pediatrics|June 1, 1992
Hypothalamic failure as a sequela of heterozygous protein C deficiency?S Schmitt, K Auberger, T Fendel, et al.
European Journal of Pediatrics|January 29, 2000
The low molecular weight heparin dalteparin for prophylaxis and therapy of thrombosis in childhood: a report on 48 casesN Nohe, A Flemmer, R Rümler, et al.
Klinische Wochenschrift|July 15, 1987
[Homozygous infant in a family with hereditary protein C deficiency]G Hintz, J Weil, S Buchmann, et al.
European Journal of Pediatrics|January 29, 2000
Role of genetic prothrombotic risk factors in childhood caval vein thrombosisN Münchow, A Kosch, R Schobess, et al.
British Journal of Haematology|September 1, 1996
Prenatal diagnosis in combined antithrombin and factor V gene mutationD A Lane, K Auberger, H Ireland, et al.
Journal of Neuroimaging : Official Journal of the American Society of Neuroimaging|April 1, 1997
Brain hemangiomas of infancy. Sonographic detection and follow-upC Hundt, K Auberger, G Münch, et al.
British Journal of Haematology|December 1, 1988
Replacement therapy for a homozygous protein C deficiency-state using a concentrate of human protein C and ST Vukovich, K Auberger, J Weil, et al.
European Journal of Pediatrics|January 29, 2000
Factor V G1691A and prothrombin G20210A in childhood spontaneous venous thrombosis--evidence of an age-dependent thrombotic onset in carriers of factor V G1691A and prothrombin G20210A mutationR Schobess, R Junker, K Auberger, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Annals of Hematology|March 1, 1992
Evaluation of a new protein-C concentrate and comparison of protein-C assays in a child with congenital protein-C deficiencyK Auberger
European Journal of Pediatrics|May 2, 2000
Thrombosis of the deep cerebral veins with excessive bilateral infarction in a premature infant with the thrombogenic 4G/4G genotype of the plasminogen activator inhibitor-1F A Baumeister, K Auberger, K Schneider
European Journal of Pediatrics|June 1, 1992
Hypothalamic failure as a sequela of heterozygous protein C deficiency?S Schmitt, K Auberger, T Fendel, et al.
European Journal of Pediatrics|January 29, 2000
The low molecular weight heparin dalteparin for prophylaxis and therapy of thrombosis in childhood: a report on 48 casesN Nohe, A Flemmer, R Rümler, et al.
Klinische Wochenschrift|July 15, 1987
[Homozygous infant in a family with hereditary protein C deficiency]G Hintz, J Weil, S Buchmann, et al.
European Journal of Pediatrics|January 29, 2000
Role of genetic prothrombotic risk factors in childhood caval vein thrombosisN Münchow, A Kosch, R Schobess, et al.
British Journal of Haematology|September 1, 1996
Prenatal diagnosis in combined antithrombin and factor V gene mutationD A Lane, K Auberger, H Ireland, et al.
Journal of Neuroimaging : Official Journal of the American Society of Neuroimaging|April 1, 1997
Brain hemangiomas of infancy. Sonographic detection and follow-upC Hundt, K Auberger, G Münch, et al.
British Journal of Haematology|December 1, 1988
Replacement therapy for a homozygous protein C deficiency-state using a concentrate of human protein C and ST Vukovich, K Auberger, J Weil, et al.
European Journal of Pediatrics|January 29, 2000
Factor V G1691A and prothrombin G20210A in childhood spontaneous venous thrombosis--evidence of an age-dependent thrombotic onset in carriers of factor V G1691A and prothrombin G20210A mutationR Schobess, R Junker, K Auberger, et al.
Pageof 2