S R Poort - Concepedia

Author

S R Poort

Also Known As

Hans Vos, S Poort, S R Poort, S. Poort, S. R. Poort, S.R. POORT, S.R. Poort, Swibertus R Poort, Swibertus R. POORT, Swibertus R. Poort

Publications

Citations

H-Index

Concepts

All Affiliations

Leiden University Utrecht University Leiden University Medical Center Thrombosis Research Institute Rotterdam University of Applied Sciences

About

S R Poort is an author at Leiden University specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	13	16	1.5K
2	Public Health	4	4	366
3	Natural Sciences	3	3	222
4	Health Sciences	2	2	34
5	Allergy	1	1	126

S R Poort

Publications

1.8K

Citations

H-Index

Page 1

	Year	Citations
Increased risk of venous thrombosis in carriers of hereditary protein C deficiency defect C.F. Allaart, S R Poort, Pieter H. Reitsma, The Lancet Venous DiseaseVenous ThrombosisVenous Disease TreatmentGenetic DisorderInherited Metabolic Disease	1993	361
Prevalence of Protein C Deficiency in the Healthy Population Robert C. Tait, Isobel D. Walker, P H Reitsma, Thrombosis and Haemostasis NutritionGeneticsGenetic EpidemiologyHuman PolymorphismPathology	1995	334
Protein C Deficiency: A Database of Mutations, 1995 Update P H Reitsma, Francesca Bernardi, Rowan G. Doig, Thrombosis and Haemostasis Protein C DeficiencyGenetic DisorderGeneticsPathogenesisPathology	1995	294
Determination of Plasma Protein S - The Protein Cofactor of Activated Protein C Rogier M. Bertina, A van Wijngaarden, J Reinalda-Poot, Thrombosis and Haemostasis ImmunologyPathologyProtein CofactorPlasma Protein SProtein S	1985	126
Protein C deficiency: a database of mutations. For the Protein C & S Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis. Pieter H. Reitsma, S R Poort, Francesco Bernardi, PubMed ThrombosisLaboratory HematologyProtein C DeficiencyGenetic DisorderGenetics	1993	83
Factor XIII Val34Leu polymorphism, factor XIII antigen levels and activity and the risk of deep venous thrombosis Astrid van Hylckama Vlieg, Nantarat Komanasin, Robert A.S. Ariëns, British Journal of Haematology	2002	73
Binding of recombinant annexin V to endothelial cells: effect of annexin V binding on endothelial-cell-mediated thrombin formation Waander L. van Heerde, S R Poort, Cornelis van ′t Veer, Biochemical Journal Endothelial CellsDissociation ConstantImmunologyAnnexin VThrombosis	1994	65
Protein C Deficiency: A Database of Mutations P.H. Reitsma, S R Poort, Fernando Luiz de Melo Bernardi, Thrombosis and Haemostasis Protein C DeficiencyGenetic DisorderGeneticsMolecular GeneticsDisease Gene Identification	1993	65
Homozygosity for a Novel Missense Mutation in the Prothrombin Gene Causing a Severe Bleeding Disorder S R Poort, J. J. Michiels, P.H. Reitsma, Thrombosis and Haemostasis GeneticsImmunologyGenetic EpidemiologyPathologyProthrombin Gene	1994	39
Identification of Eight Point Mutations in Protein S Deficiency Type I – Analysis of 15 Pedigrees P H Reitsma, E. Gómez, S R Poort, Thrombosis and Haemostasis Mendelian DisorderPoint MutationsEight Point MutationsMedicineGenetics	1995	34

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