Connection
Christopher Ng to von Willebrand Diseases
This is a "connection" page, showing publications Christopher Ng has written about von Willebrand Diseases.
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2.656 |
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Ng CJ, Baker RI, Lavin M, Haberichter SL. Recommendation to adopt the type 1C VWD nomenclature into the classification of von Willebrand disease: communication from the ISTH Scientific and Standardisation Subcommittee on von Willebrand Factor. J Thromb Haemost. 2026 07; 24(7):2656-2660.
Score: 0.935
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Ng CJ, Liu A, Venkataraman S, Ashworth KJ, Baker CD, O'Rourke R, Vibhakar R, Jones KL, Di Paola J. Single-cell transcriptional analysis of human endothelial colony-forming cells from patients with low VWF levels. Blood. 2022 04 07; 139(14):2240-2251.
Score: 0.713
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Ng CJ, Di Paola J. von Willebrand Disease: Diagnostic Strategies and Treatment Options. Pediatr Clin North Am. 2018 06; 65(3):527-541.
Score: 0.546
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Cox AA, Liu A, Ng CJ. Clusterin knockdown has effects on intracellular and secreted von Willebrand factor in human umbilical vein endothelial cells. PLoS One. 2024; 19(2):e0298133.
Score: 0.203
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Rao ES, Ng CJ. Current approaches to diagnostic testing in von Willebrand Disease. Transfus Apher Sci. 2018 Aug; 57(4):463-465.
Score: 0.138
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White-Adams TC, Ng CJ, Jacobi PM, Haberichter SL, Di Paola JA. Mutations in the D'D3 region of VWF traditionally associated with type 1 VWD lead to quantitative and qualitative deficiencies of VWF. Thromb Res. 2016 Sep; 145:112-8.
Score: 0.120