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B Zieger

Showing results (51-60 of 76) with videos related to

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Thrombosis Research|July 1, 1997
New families with von Willebrand disease type 2M (Vicenza)B Zieger, U Budde, U Jessat, et al.
Hamostaseologie|May 1, 2009
Lepirudin treatment in a boy with suspected HIT II after surgery because of tetralogy of FallotChristof Andreas Hanke, K Barth, L Nakamura, et al.
Vaccine|August 5, 2000
Can monovalent hepatitis A and B vaccines be replaced by a combined hepatitis A/B vaccine during the primary immunization course?B Kallinowski, A Knöll, E Lindner, et al.
Klinische Padiatrie|April 20, 2012
Homozygous point mutations in platelet glycoprotein ITGA2B gene as cause of Glanzmann thrombasthenia in 2 familiesK Sandrock, S Halimeh, V Wiegering, et al.
Radiology|January 14, 1999
Reflux in young patients: comparison of voiding US of the bladder and retrovesical space with echo enhancement versus voiding cystourethrography for diagnosisK Darge, J Troeger, T Duetting, et al.
Klinische Padiatrie|May 28, 2013
Molecular genetic analysis of a patient with moderate hemophilia A and psychomotor developmental delayM Gothwal, L Nakamura, I Hainmann, et al.
Human Genetics|June 1, 1995
Identification of a candidate missense mutation in a family with von Willebrand disease type IICR Schneppenheim, K B Thomas, S Krey, et al.
Klinische Padiatrie|May 14, 2009
Lepirudin treatment in a girl with iliac vein thrombosis, severe pulmonary embolism and suspected heparin-induced thrombocytopenia (HIT) IIK N Walter, M Erlacher, M Uhl, et al.
Klinische Padiatrie|June 2, 2010
Compound heterozygous mutations in 2 siblings with Hermansky-Pudlak syndrome type 1 (HPS1)K Sandrock, I Bartsch, N Rombach, et al.
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|September 29, 2000
[Hypertrophic pyloric stenosis: sonographic monitoring of conservative therapy with intravenous atropine sulfate]I Theobald, W K Rohrschneider, P E Meissner, et al.
Pageof 8

Showing results (51-60 of 76) with videos related to

Sort By:
Pageof 8
Thrombosis Research|July 1, 1997
New families with von Willebrand disease type 2M (Vicenza)B Zieger, U Budde, U Jessat, et al.
Hamostaseologie|May 1, 2009
Lepirudin treatment in a boy with suspected HIT II after surgery because of tetralogy of FallotChristof Andreas Hanke, K Barth, L Nakamura, et al.
Vaccine|August 5, 2000
Can monovalent hepatitis A and B vaccines be replaced by a combined hepatitis A/B vaccine during the primary immunization course?B Kallinowski, A Knöll, E Lindner, et al.
Klinische Padiatrie|April 20, 2012
Homozygous point mutations in platelet glycoprotein ITGA2B gene as cause of Glanzmann thrombasthenia in 2 familiesK Sandrock, S Halimeh, V Wiegering, et al.
Radiology|January 14, 1999
Reflux in young patients: comparison of voiding US of the bladder and retrovesical space with echo enhancement versus voiding cystourethrography for diagnosisK Darge, J Troeger, T Duetting, et al.
Klinische Padiatrie|May 28, 2013
Molecular genetic analysis of a patient with moderate hemophilia A and psychomotor developmental delayM Gothwal, L Nakamura, I Hainmann, et al.
Human Genetics|June 1, 1995
Identification of a candidate missense mutation in a family with von Willebrand disease type IICR Schneppenheim, K B Thomas, S Krey, et al.
Klinische Padiatrie|May 14, 2009
Lepirudin treatment in a girl with iliac vein thrombosis, severe pulmonary embolism and suspected heparin-induced thrombocytopenia (HIT) IIK N Walter, M Erlacher, M Uhl, et al.
Klinische Padiatrie|June 2, 2010
Compound heterozygous mutations in 2 siblings with Hermansky-Pudlak syndrome type 1 (HPS1)K Sandrock, I Bartsch, N Rombach, et al.
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|September 29, 2000
[Hypertrophic pyloric stenosis: sonographic monitoring of conservative therapy with intravenous atropine sulfate]I Theobald, W K Rohrschneider, P E Meissner, et al.
Pageof 8