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K Auberger

Showing results (11-20 of 19) with videos related to

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Arteriosclerosis, Thrombosis, and Vascular Biology|October 16, 1999
Prothrombin G20210A gene mutation and further prothrombotic risk factors in childhood thrombophiliaR Junker, H G Koch, K Auberger, et al.
European Journal of Pediatrics|January 29, 2000
Prevalence and outcome of intracranial haemorrhage in haemophiliacs--a survey of the paediatric group of the German Society of Thrombosis and Haemostasis (GTH)J Klinge, K Auberger, G Auerswald, et al.
The Clinical Investigator|January 1, 1994
High-dose intravenous immunoglobulins in the treatment of adolescent and adult HIV-infected hemophiliacsU Wintergerst, K Niinivaara-Kreuzer, G Notheis, et al.
Human Mutation|January 1, 1994
(ATT) trinucleotide repeats in the antithrombin gene and their use in determining the origin of repeated mutationsR J Olds, D A Lane, V Chowdhury, et al.
European Journal of Pediatrics|November 1, 1996
Inherited defects of the protein C anticoagulant system in childhood thrombo-embolismU Nowak-Göttl, K Auberger, U Göbel, et al.
Thrombosis and Haemostasis|March 1, 2000
Thrombolysis in newborns and infantsU Nowak-Göttl, K Auberger, S Halimeh, et al.
European Journal of Pediatrics|January 29, 2000
The 677T genotype of the common MTHFR thermolabile variant and fasting homocysteine in childhood venous thrombosisH G Koch, P Nabel, R Junker, et al.
Thrombosis and Haemostasis|August 1, 1994
Homozygous antithrombin deficiency: report of two new cases (99 Leu to Phe) associated with arterial and venous thrombosisV Chowdhury, D A Lane, B Mille, et al.
Seminars in Thrombosis and Hemostasis|November 25, 2000
Molecular biology and clinical manifestation of hereditary factor VII deficiencyF H Herrmann, K Wulff, K Auberger, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Arteriosclerosis, Thrombosis, and Vascular Biology|October 16, 1999
Prothrombin G20210A gene mutation and further prothrombotic risk factors in childhood thrombophiliaR Junker, H G Koch, K Auberger, et al.
European Journal of Pediatrics|January 29, 2000
Prevalence and outcome of intracranial haemorrhage in haemophiliacs--a survey of the paediatric group of the German Society of Thrombosis and Haemostasis (GTH)J Klinge, K Auberger, G Auerswald, et al.
The Clinical Investigator|January 1, 1994
High-dose intravenous immunoglobulins in the treatment of adolescent and adult HIV-infected hemophiliacsU Wintergerst, K Niinivaara-Kreuzer, G Notheis, et al.
Human Mutation|January 1, 1994
(ATT) trinucleotide repeats in the antithrombin gene and their use in determining the origin of repeated mutationsR J Olds, D A Lane, V Chowdhury, et al.
European Journal of Pediatrics|November 1, 1996
Inherited defects of the protein C anticoagulant system in childhood thrombo-embolismU Nowak-Göttl, K Auberger, U Göbel, et al.
Thrombosis and Haemostasis|March 1, 2000
Thrombolysis in newborns and infantsU Nowak-Göttl, K Auberger, S Halimeh, et al.
European Journal of Pediatrics|January 29, 2000
The 677T genotype of the common MTHFR thermolabile variant and fasting homocysteine in childhood venous thrombosisH G Koch, P Nabel, R Junker, et al.
Thrombosis and Haemostasis|August 1, 1994
Homozygous antithrombin deficiency: report of two new cases (99 Leu to Phe) associated with arterial and venous thrombosisV Chowdhury, D A Lane, B Mille, et al.
Seminars in Thrombosis and Hemostasis|November 25, 2000
Molecular biology and clinical manifestation of hereditary factor VII deficiencyF H Herrmann, K Wulff, K Auberger, et al.
Pageof 2