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J C Eikenboom

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Best Practice & Research. Clinical Haematology|November 1, 2001

Congenital von Willebrand disease type 3: clinical manifestations, pathophysiology and molecular biologyJ C Eikenboom

Analytical Biochemistry|February 15, 1997

Separating short tandem repeat polymorphisms on microgelD Guo, J C Eikenboom, R M Bertina

Haemostasis|January 1, 1992

Value of the patient interview: all but consensus among haemostasis expertsJ C Eikenboom, F R Rosendaal, E Briët

Annals of Hematology|March 1, 1994

Seeming homozygosity in type-IIB von Willebrand's disease due to a polymorphism within the sequence of a commonly used primerJ C Eikenboom, P H Reitsma, E Briët

Thrombosis and Haemostasis|February 3, 1992

Peri-operative replacement therapy with factor VII concentrate in a patient with severe factor VII deficiencyJ C Eikenboom, C F Bos, E Briët

Thrombosis and Haemostasis|August 1, 1991

Paroxysmal finger haematoma: a neglected syndromeJ C Eikenboom, S C Cannegieter, E Briët

Haemophilia : the Official Journal of the World Federation of Hemophilia|May 24, 2016

The inheritance and molecular genetics of von Willebrand's diseaseJ C Eikenboom, P H Reitsma, E Briët

Thrombosis and Haemostasis|November 1, 2000

Grossly abnormal proteolysis of von Willebrand factor (VWF) in a patient heterozygous for a gene deletion and mutation in the dimerization area of VWFG Castaman, J C Eikenboom, A Lattuada, et al.

Thrombosis and Haemostasis|August 26, 2000

Pregnancy in women with type 1 von Willebrand disease caused by heterozygosity for von Willebrand factor mutation C1130FG Castaman, J C Eikenboom, A Contri, et al.

British Journal of Haematology|May 3, 2000

Autosomal dominant type 1 von willebrand disease due to G3639T mutation (C1130F) in exon 26 of von Willebrand factor gene: description of five Italian families and evidence for a founder effectG Castaman, J C Eikenboom, E Missiaglia, et al.

Pageof 4

Search research articles

Showing results (1-10 of 33) with videos related to

Sort By:

Pageof 4

Best Practice & Research. Clinical Haematology|November 1, 2001

Congenital von Willebrand disease type 3: clinical manifestations, pathophysiology and molecular biologyJ C Eikenboom

Analytical Biochemistry|February 15, 1997

Separating short tandem repeat polymorphisms on microgelD Guo, J C Eikenboom, R M Bertina

Haemostasis|January 1, 1992

Value of the patient interview: all but consensus among haemostasis expertsJ C Eikenboom, F R Rosendaal, E Briët

Annals of Hematology|March 1, 1994

Seeming homozygosity in type-IIB von Willebrand's disease due to a polymorphism within the sequence of a commonly used primerJ C Eikenboom, P H Reitsma, E Briët

Thrombosis and Haemostasis|February 3, 1992

Peri-operative replacement therapy with factor VII concentrate in a patient with severe factor VII deficiencyJ C Eikenboom, C F Bos, E Briët

Thrombosis and Haemostasis|August 1, 1991

Paroxysmal finger haematoma: a neglected syndromeJ C Eikenboom, S C Cannegieter, E Briët

Haemophilia : the Official Journal of the World Federation of Hemophilia|May 24, 2016

The inheritance and molecular genetics of von Willebrand's diseaseJ C Eikenboom, P H Reitsma, E Briët

Thrombosis and Haemostasis|November 1, 2000

Grossly abnormal proteolysis of von Willebrand factor (VWF) in a patient heterozygous for a gene deletion and mutation in the dimerization area of VWFG Castaman, J C Eikenboom, A Lattuada, et al.

Thrombosis and Haemostasis|August 26, 2000

Pregnancy in women with type 1 von Willebrand disease caused by heterozygosity for von Willebrand factor mutation C1130FG Castaman, J C Eikenboom, A Contri, et al.

British Journal of Haematology|May 3, 2000

Autosomal dominant type 1 von willebrand disease due to G3639T mutation (C1130F) in exon 26 of von Willebrand factor gene: description of five Italian families and evidence for a founder effectG Castaman, J C Eikenboom, E Missiaglia, et al.

Pageof 4