Amino acid dimorphism in IL1A is detectable by PCR amplificationVELDEN, P. A. V. D; REITSMA, P. H.Human molecular genetics (Print). 1993, Vol 2, Num 10, issn 0964-6906, p. 1753Article

Double strand conformation polymorphism (DSCP) detects two point mutations at codon 280 (AAC→ATC) and at codon 431 (TAC→AAC) of the blood coagulation factor VIII genePIENEMAN, W. C; REITSMA, P. H; BRIËT, E et al.Thrombosis and haemostasis. 1993, Vol 69, Num 5, pp 473-475, issn 0340-6245Article

The mutational demography of protein C deficiencyKRAWCZAK, M; REITSMA, P. H; COOPER, D. N et al.Human genetics. 1995, Vol 96, Num 2, pp 142-146, issn 0340-6717Article

Protein C deficiency : from gene defects to diseaseREITSMA, P. H.Thrombosis and haemostasis. 1997, Vol 78, Num 1, pp 344-350, issn 0340-6245Conference Paper

MspI RFLP in intron 8 of the human protein C geneKOENHEN, E; BERTINA, R. M; REITSMA, P. H et al.Nucleic acids research. 1989, Vol 17, Num 20, issn 0305-1048, 8401Article

The spectrum of genetic defects in a panel of 40 dutch families within symptomatic protein C deficiency type I heterogeneity and founder effectsREITSMA, P. H; ALLAART, C. F; BERTINA, R. M et al.Blood. 1991, Vol 78, Num 4, pp 890-894, issn 0006-4971Article

Localization of transcription initiation sites in the human coagulation factor IX geneREIJNEN, M. J; BERTINA, R. M; REITSMA, P. H et al.FEBS letters. 1990, Vol 270, Num 1-2, pp 207-210, issn 0014-5793, 4 p.Article

Characterization of a large chromosomal deletion in the PROS1 gene of a patient with protein S deficiency type I using long PCRHOLMES, Z. R; BERTINA, R. M; REITSMA, P. H et al.British journal of haematology. 1996, Vol 92, Num 4, pp 986-991, issn 0007-1048Article

Inherited prethrombotic disorders and infectious purpuraWESTENDORP, R. G. J; REITSMA, P. H; BERTINA, R. M et al.Thrombosis and haemostasis. 1996, Vol 75, Num 6, pp 899-901, issn 0340-6245Article

Seeming homozygosity in type-IIB von Willebrand's disease due to a polymorphism within the sequence of a commonly used primerEIKENBOOM, J. C. J; REITSMA, P. H; BRIËT, E et al.Annals of hematology (Print). 1994, Vol 68, Num 3, pp 139-141, issn 0939-5555Article

Two RFLPS ∼ 7 kb 5' of the human protein C geneLINTEL HEKKERT, W. T; BERTINA, R. M; REITSMA, P. H et al.Nucleic acids research. 1988, Vol 16, Num 24, issn 0305-1048, 11849 [1 p.]Article

Inhalation of activated protein C inhibits endotoxin-induced pulmonary inflammation in mice independent of neutrophil recruitmentSLOFSTRA, S. H; GROOT, A. P; MARIS, N. A et al.British journal of pharmacology. 2006, Vol 149, Num 6, pp 740-746, issn 0007-1188, 7 p.Article

Thermolabile methylenetetrahydrofolate reductase and factor V Leiden in the risk of deep-vein thrombosisKLUIJTMANS, L. A. J; HEIJER, M. D; REITSMA, P. H et al.Thrombosis and haemostasis. 1998, Vol 79, Num 2, pp 254-258, issn 0340-6245Article

Protein S deficiency : A database of mutations : For the Plasma Coagulation Inhibitors Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and HaemostasisGANDRILLE, S; BORGEL, D; FORMSTONE, C et al.Thrombosis and haemostasis. 1997, Vol 77, Num 6, pp 1201-1214, issn 0340-6245Article

Factor V Leiden (resistance to activated protein C) increases the risk of myocardial infarction in young womenROSENDAAL, F. R; SISCOVICK, D. S; SCHWARTZ, S. M et al.Blood. 1997, Vol 89, Num 8, pp 2817-2821, issn 0006-4971Article

Rat ferritin-H : cDNA cloning, differential expression and localization during hepatocarcinogenesisWU, C.-G; GROENINK, M; BOSMA, A et al.Carcinogenesis (New York. Print). 1997, Vol 18, Num 1, pp 47-52, issn 0143-3334Article

Tissue factor expression during monocyte-macrophage differentiationVAN DEN EIJNDEN, M. M. E. D; STEENHAUER, S.-I; REITSMA, P. H et al.Thrombosis and haemostasis. 1997, Vol 77, Num 6, pp 1129-1136, issn 0340-6245Article

Apparent different thrombotic tendency in patients with factor V Leiden and protein C deficiency due to selection of patientsLENSEN, R. P. M; ROSENDAAL, F. R; KOSTER, T et al.Blood. 1996, Vol 88, Num 11, pp 4205-4208, issn 0006-4971Article

Rapid identification of gene defects in protein C deficiency by temperature gradient gel electrophoresisHERNANDEZ, A; UHRBERG, M; ENCZMANN, J et al.Blood coagulation & fibrinolysis. 1995, Vol 6, Num 1, pp 23-30, issn 0957-5235Article

Protein C deficiency in a controlled series of unselected outpatients : an infrequent but clear risk factor for venous thrombosis (Leiden thrombophilia study)KOSTER, T; ROSENDAAL, F. R; BRIËT, E et al.Blood. 1995, Vol 85, Num 10, pp 2756-2761, issn 0006-4971Article

Mutation in blood coagulation factor V associated with resistance to activated protein CBERTINA, R. M; KOELEMAN, B. P. C; KOSTER, T et al.Nature (London). 1994, Vol 369, Num 6475, pp 64-67, issn 0028-0836Article

Haemophilia B : database of point mutations and short additions and deletions : second editionGIANNELLI, F; GREEN, P. M; SOMMER, S et al.Nucleic acids research. 1991, Vol 19, pp 2193-2219, issn 0305-1048, 27 p., SUPArticle

Intron-exon organization of the human gene coding for the lipoprotein-associated coagulation inhibitor : the factor Xa dependent inhibitor of the extrinsic pathway of coagulationVAN DER LOGT, C. P. E; REITSMA, P. H; BERTINA, R. M et al.Biochemistry (Easton). 1991, Vol 30, Num 6, pp 1571-1577, issn 0006-2960, 7 p.Article

A Dutch family with moderately severe hemophilia B (factor IX_Heerde) has a missense mutation identical to that of factor IX_London2POORT, S. R; BRIET, E; BERTINA, R. M et al.Nucleic acids research. 1989, Vol 17, Num 9, issn 0305-1048, 3614 [1 p.]Article

Two genes homologous with human protein s cDNA are located on chromosome 3PLOOS VAN AMSTED, J. K; VAN DER ZANDEN, A. L; BAKKER, E et al.Thrombosis and haemostasis. 1987, Vol 58, Num 4, pp 982-987, issn 0340-6245Article