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Consecutive publication list on the project and/or work referring to the project (in descending order)
16. Von Krogh A-S, Quist-Paulsen P, Waage A, Langseth ØO, Thorstensen K, Brudevold R, Tjønnfjord GE, Largiadèr CR, Lämmle B, Kremer Hovinga JA. High prevalence of hereditary thrombotic thrombocytopenic purpura in Central Norway: from clinical observation to evidence.
15. Von Krogh A-S, Kremer Hovinga JA, Romundstad PR, Roten LT, Lämmle B, Waage A, Quist-Paulsen P. ADAMTS13 gene variants and function in women with preeclampsia: a population-based nested case-control study from the HUNT study.
14. Von Auer C, von Krogh A-S, Kremer Hovinga JA, Lämmle B. Current insights into thrombotic microangiopathies: Thrombotic thrombocytopenic purpura and pregnancy.
13. Raval JS, Padmanabhan A, Kremer Hovinga JA, Kiss JE. Development of a clinically significant ADAMTS13 inhibitor in a patient with hereditary thrombotic thrombocytopenic purpura. Am J Hematol 2015;90:E22
12. Falter T, Kremer Hovinga JA, Lackner K, Füllemann H-G, Lämmle B, Scharrer I. Late onset and pregnancy-induced congenital thrombotic thrombocytopenic purpura. Haemostaseologie 2014;34:244–24
11. Von Krogh A-S, Kremer Hovinga JA, Tjønnfjord GE, Ringen IM, Lämmle B, Waage A, Quist-Paulsen P. The impact of congenital thrombotic thrombocytopenic purpura on pregnancy complications. Thromb Haemost 2014;111:1180–1183
8. Rank CU, Kremer Hovinga JA, Taleghani MM, Lämmle B, Gøtze JP, Nielsen OJ. Congenital thrombotic thrombocytopenic purpura caused by new compound heterozygous mutations of the ADAMTS13 gene. Eur J Haematol. 2014;92:168-71
5. Mansouri Taleghani M, von Krogh A-S, Fujimura Y, George JN, Hrachovinova I, Knöbl PN, Quist-Paulsen P, Schneppenheim R, Lämmle B, Kremer Hovinga JA. Hereditary Thrombotic Thrombocytopenic Purpura (Upshaw-Schulman syndrome) and the hereditary TTP registry.
4. Deal T, Kremer Hovinga JA, Marques MB, Adamski J. Novel ADAMTS13 Mutations in an Obstetric Patient with Upshaw-Schulman Syndrome. J Clin Apher 2013;28:311-16
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